Category: nitriles-buliding-blocks

Nitrile is any organic compound with a −C≡N functional group. 105-34-0, formula is C4H5NO2, Name is Methyl 2-cyanoacetate.The prefix cyano- is used interchangeably with the term nitrile in literature. Computed Properties of 105-34-0.

Shin, Sangbin;Sim, Eunji;Lee, Wonjoo;Paik, Hyun-jong;Yu, Youngchang;Ahn, Dowon research published 《 Synthesis and reactivity of novel cinnamonitrile derivatives as reactive UV stabilizers for enhanced light protection and performance of coatings》, the research content is summarized as follows. UV light is generally harmful to human health and organic compounds (for example, plastics) as it deteriorates the long-term stability via photodegradation Thus, an efficient strategy for reducing light-induced damage is the key to maximizing the operation lifetime or durability of materials. The most common means of preventing UV light-induced damage is by adding compounds that possess excellent UV absorbing capability. In this study, novel cinnamonitrile derivatives were designed and synthesized for their application as UV absorbers in pressure-sensitive adhesives. Absorption wavelengths were finely tuned by simple structural modification, and better molar absorptivity was obtained. The hydroxyhexyl functional group affixed into the cinnamonitrile core granted superior solubility (>10 weight%) in common organic solvents and acrylic monomers/resins, instigating enhanced UV blocking and visible light transparency. Further, to enhance the solubility and long-term stability of UV absorbers within a network, hydroxyhexyl-functionalized cinnamonitrile UV absorber was incorporated into urethane-based crosslinkers. Covalently attached reactive UV absorbers improved the adhesion property even at a high loading of UV absorber and remarkable phys. persistence within the network.

Computed Properties of 105-34-0, Methyl cyanoacetate is an alkyl cyanoacetate ester.
Methyl cyanoacetate is the intermediate product in pharmaceutical organic synthesis as well as in the synthesis of some biologically active compounds used in agriculture. It undergoes calcite or fluorite catalyzed Knövenagel condensation with aromatic aldehydes, giving the corresponding arylidenemalononitriles and (E)-α -cyanocinnamic esters.
Methyl Cyanoacetate is often used as a nucleophile in the electrochemical oxidation of catechols. Methyl Cyanoacetate is also a reagent in the synthesis of Methyl 2-Amino-4-trifluoromethylthiophene-3-carboxylate (M287290); a compound used in the synthesis of DPP-IV inhibitors for treating type 2 diabetes., 105-34-0.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Nitrile is any organic compound with a −C≡N functional group. 20099-89-2, formula is C9H6BrNO, Name is 4-(2-Bromoacetyl)benzonitrile.The prefix cyano- is used interchangeably with the term nitrile in literature. Name: 4-(2-Bromoacetyl)benzonitrile.

Shin, Young Sup;Lee, Jun Young;Noh, Soojin;Kwak, Yoonna;Jeon, Sangeun;Kwon, Sunoh;Jin, Young-hee;Jang, Min Seong;Kim, Seungtaek;Song, Jong Hwan;Kim, Hyoung Rae;Park, Chul Min research published 《 Discovery of cyclic sulfonamide derivatives as potent inhibitors of SARS-CoV-2》, the research content is summarized as follows. Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) continues to spread worldwide, with 25 million confirmed cases and 800 thousand deaths. Effective treatments to target SARS-CoV-2 are urgently needed. In the present study, we have identified a class of cyclic sulfonamide derivatives as novel SARS-CoV-2 inhibitors. Compound 13c of the synthesized compounds exhibited robust inhibitory activity (IC₅₀ = 0.88μM) against SARS-CoV-2 without cytotoxicity (CC₅₀ > 25μM), with a selectivity index (SI) of 30.7. In addition, compound 13c exhibited high oral bioavailability (77%) and metabolic stability with good safety profiles in hERG and cytotoxicity studies. The present study identified that cyclic sulfonamide derivatives are a promising new template for the development of anti-SARS-CoV-2 agents.

20099-89-2, 4-(2-Bromoacetyl)benzonitrile, also known as 2-Bromo-4′ -cyanoacetophenone, is a useful research compound. Its molecular formula is C9H6BrNO and its molecular weight is 224.05 g/mol. The purity is usually 95%.
2-Bromo-4′ -cyanoacetophenone can be synthesized from ethylbenzene via aerobic photooxidation using aqueous HBr.
4-(2-Bromoacetyl)benzonitrile is useful for the irreversible inhibitory activity of Glycogen synthase kinase 3 (GSK-3). Phenylhalomethylketones can be used in the study of novel GSK-3 inhibitors., Name: 4-(2-Bromoacetyl)benzonitrile

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Industrially, the main methods for producing nitriles are ammoxidation and hydrocyanation. 31643-49-9, formula is C8H3N3O2, Name is 4-Nitrophthalonitrile. Both routes are green in the sense that they do not generate stoichiometric amounts of salts. Application In Synthesis of 31643-49-9.

Singh, Ajit Shankar;Shukla, S. K.;Mishra, Preeti;Pandey, A. K. research published 《 Synthesis and thermal evaluation of novel mono- and bis-adamantylated resorcinol-based phthalonitrile resins with enhanced solubility》, the research content is summarized as follows. Phthalonitrile (PN) resins are high-temperature-resistant thermosetting polymers which find applications in military as well as aerospace owing to their outstanding performance. At present, most of the PN resins are melt-processed and cured at high temperature via resin transfer molding owing to their poor solubility in common organic solvents. In the present, embodiment efforts have been made to change the PN resin backbone with adamantane as potential functionality. Mono- and novel bis-adamantylated resorcinols 1a and 1b have been synthesized via Amberlyst-15 solid acid resin-catalyzed Friedel-Crafts alkylation reaction, as precursor material for the synthesis of novel phthalonitrile (PN) resin monomers 2a and 2b, resp. The study includes structural and thermal characterization of resin monomers 2a and 2b along with their solubility in common organic solvents. These resins when cured to their thermosets have demonstrated thermal stability ~723 K (5% mass loss) with no glass transition temperature (Tg) up to 673 K. The resin monomers show very good solubility in industry-friendly organic solvents like acetone, Et acetate, Me Et ketone and Me iso-Bu ketone.

Application In Synthesis of 31643-49-9, 4-Nitrophthalonitrile, also known as 4-Nitrophthalonitrile, is a useful research compound. Its molecular formula is C8H3N3O2 and its molecular weight is 173.13 g/mol. The purity is usually > 95%.
4-Nitrophthalonitrile is a chemical substance that can be synthesized by the reaction of sodium carbonate with 3,4,5-trimethoxybenzyl alcohol. It can also be prepared using nitro phenol and sodium hydroxide. 4-Nitrophthalonitrile has been shown to have high photochemical activity in the presence of light. The frequency shift of its infrared spectrum is indicative of a nucleophilic addition reaction mechanism. 4-Nitrophthalonitrile has been used as an intermediate for producing other chemicals, such as herbicides and pharmaceuticals., 31643-49-9.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Nitrile is any organic compound with a −C≡N functional group. 1835-49-0, formula is C8F4N2, Name is Tetrafluoroterephthalonitrile.The prefix cyano- is used interchangeably with the term nitrile in literature. Recommanded Product: Tetrafluoroterephthalonitrile.

Sizov, Victor E.;Zefirov, Vadim V.;Volkova, Yulia A.;Gusak, Danil I.;Kharitonova, Elena P.;Ponomarev, Igor I.;Gallyamov, Marat O. research published 《 Celgard/ PIM -1 proton conducting composite membrane with reduced vanadium permeability》, the research content is summarized as follows. Renewable energy systems need efficient and cheap storage devices and vanadium redox flow batteries (VRB) may become one of them. However, better performance of VRB membranes yet should be achieved. Novel composite Celgard-based films coated with PIM-1 for aqueous electrolyte VRB applications are presented. Two types of the composites with different PIM-1 loadings are obtained. Their properties are studied and compared with the original Celgard films. The deposited PIM-1 forms a smooth layer on the outer Celgard surface and penetrates inside the porous matrix, thus significantly reducing the pores diameter and affecting the transport properties of the composite film. The nanoporous structure of PIM-1 permits size-screening of H₃O⁺/hydrated vanadium ions when used in aqueous vanadium redox flow batteries applications, which allows to tailor the membrane permeability for the two types of ions and, therefore, to increase its selectivity from 4.3 x 10⁶ to 1.3 x 10⁷ mS min cm^-3, while maintaining high proton conductivity

Recommanded Product: Tetrafluoroterephthalonitrile, Tetrafluoroterephthalonitrile can react with alkyl grignard reagents to form 4-alkyltetraflurorobenzonitriles. It acts as a four electron donor ligand. Tetrafluoroterephthalonitrile can be used to synthesize polymers of intrinsic microporosity. It has been used to study UV rearranged polymers of teh PIM-1 type membrane for the efficient separation of H2 and CO2.
Tetrafluoroterephthalonitrile reacts with alkyl Grignard reagents to form corresponding 4-alkyltetrafluorobenzonitriles. Tetrafluoroterephthalonitrile acts as a four-electron donor ligand and forms tungsten(II)η 2-nitrile complexes.
Tetrafluoroterephthalonitrile is a hydroxyl group-containing organic chemical compound . It has been used in analytical chemistry as a reagent for the determination of peptide binding constants and disulfide bonds. Tetrafluoroterephthalonitrile binds to nucleophilic sites on proteins, such as the pim-1 protein, and can be used to transport other molecules across cell membranes. In addition, it has been used to produce polymers for use in analytical chemistry. This chemical is also able to bind with magnetic particles under constant pressure conditions, which makes it useful for optical sensor applications. , 1835-49-0.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Industrially, the main methods for producing nitriles are ammoxidation and hydrocyanation. 3032-92-6, formula is C9H5N, Name is 4-Ethynylbenzonitrile. Both routes are green in the sense that they do not generate stoichiometric amounts of salts. COA of Formula: C9H5N.

Reddy, Mandapati Bhargava;Prasanth, Kesavan;Anandhan, Ramasamy research published 《 Controlled Photochemical Synthesis of Substituted Isoquinoline-1,3,4(2H)-triones, 3-Hydroxyisoindolin-1-ones, and Phthalimides via Amidyl Radical Cyclization Cascade》, the research content is summarized as follows. A controlled radical cyclization cascade of isoquinoline-1,3,4(2H)-triones I(R = H, 7-Cl, 7-Br,6-Cl), 3-hydroxyisoindolin-1-ones II (R¹ = Ph, 3-chloro-4-fluorophenyl, cyclopentyl, cyclohexyl, etc.; R² = Ph, Bu, 4-phenylphenyl, naphthalen-1-yl, etc.; R³ = H, 5-Cl, 6-Br), and phthalimides III from o-alkynylated benzamides R⁴-2-R²CCC₆H₃C(O)NHR¹ (R⁴ = H, 4-Cl, 5-Br) by metal-free photoredox catalyzed amidyl N-centered radical addition to the C-C triple bond using the proton-coupled electron transfer (PCET) process under mild reaction conditions was reported. A time tunable synthesis of 3-hydroxyisoindolin-1-ones II and phthalimides III via β-carbonyl-C(sp³) bond cleavage was also achieved under visible light irradiation A mechanistic rationale for the radical cyclization cascade is supported by various control and quenching experiments as well as EPR studies.

COA of Formula: C9H5N, 4-Ethynylbenzonitrile is a simple benzyl alkyne compound potentially useful as a synthetic fragment and as a test compound for cross-coupling protocols. 4-Ethynylbenzonitrile has been described as a model compound for studying hydrogen bond formation in multifunctional molecules, as it contains four hydrogen bonding sites of which three are π-acceptors.

4-Ethynylbenzonitrile is a useful research compound. Its molecular formula is C9H5N and its molecular weight is 127.14 g/mol. The purity is usually 95%., 3032-92-6.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Nitriles are found in many useful compounds. Nitrile rubber is also widely used as automotive and other seals since it is resistant to fuels and oils. Organic compounds containing multiple nitrile groups are known as cyanocarbons. 1835-49-0, formula is C8F4N2, Name is Tetrafluoroterephthalonitrile. Nitriles are found in many useful compounds. One of the most common occurrences of nitriles is in Nitrile rubber. Recommanded Product: Tetrafluoroterephthalonitrile.

Ricci, Eleonora;Benedetti, Francesco M.;Noto, Antonella;Merkel, Timothy C.;Jin, Jianyong;De Angelis, Maria Grazia research published 《 Enabling experimental characterization and prediction of ternary mixed-gas sorption in polymers: C₂H₆/CO₂/CH₄ in PIM-1》, the research content is summarized as follows. In this work, a new exptl. protocol was designed to measure sorption of ternary gas mixtures in polymer membranes for the first time. We measured the sorption isotherms of binary and ternary mixtures of C₂H₆, CO₂, and CH₄ in PIM-1, using a pressure decay apparatus, working at constant composition and variable pressure of the gas phase. The results show competitive sorption effects in all gas mixtures analyzed, affecting each species in proportion to the total sorbed concentration of the other components. It was found that the presence of C₂H₆ in the mixture reduces the sorption of both CH₄ and CO₂ to a similar extent, so that the CO₂/CH₄ solubility-selectivity is not markedly affected. The exptl. data were used to validate predictions of the Non-Equilibrium Lattice Fluid (NELF) model of binary and ternary sorption isotherms. The NELF model is generally in close agreement, both in the prediction of pressure and mixture composition effects, proving to be a reliable tool to assess mixed-gas sorption, even in complex scenarios.

1835-49-0, Tetrafluoroterephthalonitrile can react with alkyl grignard reagents to form 4-alkyltetraflurorobenzonitriles. It acts as a four electron donor ligand. Tetrafluoroterephthalonitrile can be used to synthesize polymers of intrinsic microporosity. It has been used to study UV rearranged polymers of teh PIM-1 type membrane for the efficient separation of H2 and CO2.
Tetrafluoroterephthalonitrile reacts with alkyl Grignard reagents to form corresponding 4-alkyltetrafluorobenzonitriles. Tetrafluoroterephthalonitrile acts as a four-electron donor ligand and forms tungsten(II)η 2-nitrile complexes.
Tetrafluoroterephthalonitrile is a hydroxyl group-containing organic chemical compound . It has been used in analytical chemistry as a reagent for the determination of peptide binding constants and disulfide bonds. Tetrafluoroterephthalonitrile binds to nucleophilic sites on proteins, such as the pim-1 protein, and can be used to transport other molecules across cell membranes. In addition, it has been used to produce polymers for use in analytical chemistry. This chemical is also able to bind with magnetic particles under constant pressure conditions, which makes it useful for optical sensor applications. , Recommanded Product: Tetrafluoroterephthalonitrile

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Inorganic compounds containing the −C≡N group are not called nitriles, but cyanides instead.1835-49-0, formula is C8F4N2, Name is Tetrafluoroterephthalonitrile. Though both nitriles and cyanides can be derived from cyanide salts, most nitriles are not nearly as toxic. Related Products of 1835-49-0.

Rochat, Sebastien;Tian, Mi;Atri, Ria;Mays, Timothy J.;Burrows, Andrew D. research published 《 Enhancement of gas storage and separation properties of microporous polymers by simple chemical modifications》, the research content is summarized as follows. Owing to their large surface area and good solvent processability, polymers of intrinsic microporosity (PIMs) have been widely investigated for gas storage and separation processes. In this article, we show how chem. modifying the polymers can fine-tune their properties for specific, targeted applications. We find that converting the archetypal microporous polymer PIM-1 into a polycarboxylate salt enhances its separation capabilities for H₂/CO₂ mixtures (relevant to hydrogen production), whereas appending multiple amine groups significantly improves gas separation properties for N₂/CO₂ mixtures (relevant to flue gas treatment). Adsorption-based separation processes have received less attention than size-sieving processes in porous polymeric materials, however they could provide a suitable alternative technol. to energy-intensive separation processes such as cryogenic distillation We also report the hydrogen storage properties of the modified polymers, which we find to depend on the chem. modification carried out. By coupling the simplicity of the proposed chem. modifications with the scalability and porous properties of PIMs, we provide a blueprint to create new multifunctional materials with adapted properties for targeted applications.

1835-49-0, Tetrafluoroterephthalonitrile can react with alkyl grignard reagents to form 4-alkyltetraflurorobenzonitriles. It acts as a four electron donor ligand. Tetrafluoroterephthalonitrile can be used to synthesize polymers of intrinsic microporosity. It has been used to study UV rearranged polymers of teh PIM-1 type membrane for the efficient separation of H2 and CO2.
Tetrafluoroterephthalonitrile reacts with alkyl Grignard reagents to form corresponding 4-alkyltetrafluorobenzonitriles. Tetrafluoroterephthalonitrile acts as a four-electron donor ligand and forms tungsten(II)η 2-nitrile complexes.
Tetrafluoroterephthalonitrile is a hydroxyl group-containing organic chemical compound . It has been used in analytical chemistry as a reagent for the determination of peptide binding constants and disulfide bonds. Tetrafluoroterephthalonitrile binds to nucleophilic sites on proteins, such as the pim-1 protein, and can be used to transport other molecules across cell membranes. In addition, it has been used to produce polymers for use in analytical chemistry. This chemical is also able to bind with magnetic particles under constant pressure conditions, which makes it useful for optical sensor applications. , Related Products of 1835-49-0

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Nitriles are found in many useful compounds. Nitrile rubber is also widely used as automotive and other seals since it is resistant to fuels and oils. Organic compounds containing multiple nitrile groups are known as cyanocarbons. 1835-49-0, formula is C8F4N2, Name is Tetrafluoroterephthalonitrile. Nitriles are found in many useful compounds. One of the most common occurrences of nitriles is in Nitrile rubber. Recommanded Product: Tetrafluoroterephthalonitrile.

Rong, Siyi;Su, Pengcheng;Chen, Shizheng;Jia, Miaomiao;Li, Wanbin research published 《 Sub-5 nm porous polymer decoration toward superhydrophobic MOFs with enhanced stability and processability》, the research content is summarized as follows. Metal-organic frameworks (MOFs) show great potential for various applications, but many of them suffer from the drawbacks of hydrolysis propensity and poor processability. Herein, we employ polymers of intrinsic microporosity (PIMs) with hydrophobic pores to decorate MOFs toward substantially improved water stability and shapeability. Through simple PIM-1 decoration, the sub-5 nm polymer layers can be uniformly deposited on MOF surfaces with almost no deterioration in porosity. Owing to the existence of superhydrophobic coating and the obstruction of water entrance into MOFs, the PIM-1 coated CuBTC exhibits impressive water resistance and excellent pore preservation ability after exposure in water, even in acidic and alk. solutions Moreover, polymer decoration improves the processability of MOFs, while various MOF/PIM-1 bulk wafers and oil-water separators can be obtained straightforwardly.

1835-49-0, Tetrafluoroterephthalonitrile can react with alkyl grignard reagents to form 4-alkyltetraflurorobenzonitriles. It acts as a four electron donor ligand. Tetrafluoroterephthalonitrile can be used to synthesize polymers of intrinsic microporosity. It has been used to study UV rearranged polymers of teh PIM-1 type membrane for the efficient separation of H2 and CO2.
Tetrafluoroterephthalonitrile reacts with alkyl Grignard reagents to form corresponding 4-alkyltetrafluorobenzonitriles. Tetrafluoroterephthalonitrile acts as a four-electron donor ligand and forms tungsten(II)η 2-nitrile complexes.
Tetrafluoroterephthalonitrile is a hydroxyl group-containing organic chemical compound . It has been used in analytical chemistry as a reagent for the determination of peptide binding constants and disulfide bonds. Tetrafluoroterephthalonitrile binds to nucleophilic sites on proteins, such as the pim-1 protein, and can be used to transport other molecules across cell membranes. In addition, it has been used to produce polymers for use in analytical chemistry. This chemical is also able to bind with magnetic particles under constant pressure conditions, which makes it useful for optical sensor applications. , Recommanded Product: Tetrafluoroterephthalonitrile

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Inorganic compounds containing the −C≡N group are not called nitriles, but cyanides instead.105-34-0, formula is C4H5NO2, Name is Methyl 2-cyanoacetate. Though both nitriles and cyanides can be derived from cyanide salts, most nitriles are not nearly as toxic. Formula: C4H5NO2.

Rouifi, Z.;Benhiba, F.;El Faydy, M.;Laabaissi, T.;Oudda, H.;Lakhrissi, B.;Guenbour, A.;Warad, I.;Zarrouk, A. research published 《 Electrochemical and theoretical studies of hydroxyquinoline grafted triazole derivatives as corrosion inhibitors for carbon steel in sulfuric acid solution》, the research content is summarized as follows. The inhibition capacity of carbon steel (CS) in 0.5M H₂SO₄ by three 8-hydroxyquinoline grafted triazole derivatives (EHTC, AHTC, and MHTC) have been investigated using electrochem. impedance spectroscopy (EIS), potentiodynamic polarization (PPD), and weight loss measurements (WLM) at 298 K. Generally, the results clearly show that the inhibition performance (η %) increases with an increase in the concentration of EHTC, MHTC, and AHTC, reaching a maximum value of 95.5% (EHTC), 95.1% (MHTC), and 94.1% (AHTC) at the optimal concentration (10^-3 M) for PPD tech. The PPD shows that EHTC, AHTC, and MHTC behave as mixed-type inhibitors. In addition, the inhibitor obeys the single layer adsorption isotherm of Langmuir. SEM (SEM) anal. of the CS has also been investigated and discussed. The theor. calculations and MD simulations show a better correlation with the exptl. results for the studied triazole derivatives

105-34-0, Methyl cyanoacetate is an alkyl cyanoacetate ester.
Methyl cyanoacetate is the intermediate product in pharmaceutical organic synthesis as well as in the synthesis of some biologically active compounds used in agriculture. It undergoes calcite or fluorite catalyzed Knövenagel condensation with aromatic aldehydes, giving the corresponding arylidenemalononitriles and (E)-α -cyanocinnamic esters.
Methyl Cyanoacetate is often used as a nucleophile in the electrochemical oxidation of catechols. Methyl Cyanoacetate is also a reagent in the synthesis of Methyl 2-Amino-4-trifluoromethylthiophene-3-carboxylate (M287290); a compound used in the synthesis of DPP-IV inhibitors for treating type 2 diabetes., Formula: C4H5NO2

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Nitriles used to be known as cyanides; the smallest organic nitrile is ethanenitrile, CH3CN, (old name: methyl cyanide or acetonitrile – and sometimes now called ethanonitrile). 3032-92-6, formula is C9H5N, Name is 4-Ethynylbenzonitrile. Nitriles are found in many useful compounds, including methyl cyanoacrylate, used in super glue, and nitrile rubber, a nitrile-containing polymer used in latex-free laboratory and medical gloves. SDS of cas: 3032-92-6.

Ru, Guang-Xin;Zhang, Meng;Zhang, Ting-Ting;Jiang, Xiao-Lei;Gao, Guang-Qin;Zhu, Xiu-Hong;Wang, Shun;Fan, Cai-Ling;Li, Xiao;Shen, Wen-Bo research published 《 Copper catalyzed dearomatization by Michael-type addition of indolyl ynones: divergent synthesis of functionalized spiroindoles and cyclopenta[c]quinolin-3-ones》, the research content is summarized as follows. Described herein is a novel copper-catalyzed multifunctionalization of alkyne-tethered indoles, allowing the practical and efficient synthesis of a diverse array of valuable dihalogen-substituted spiroindoles containing tetrasubstituted alkenes which can be readily functionalized further to obtain various spiroindolines. The construction of synthetically challenging quaternary spirocyclic carbons and tetrasubstituted alkenes is easily achieved in a single operation. Importantly, an unexpected dearomatization of alkyne-tethered indoles via Michael-type addition is involved in this tandem sequence. Furthermore, this Cu catalysis is also applicable to the regioselective synthesis of cyclopenta[c]quinolin-3-ones from readily available indolyl ynone homologues by skeletal rearrangement.

SDS of cas: 3032-92-6, 4-Ethynylbenzonitrile is a simple benzyl alkyne compound potentially useful as a synthetic fragment and as a test compound for cross-coupling protocols. 4-Ethynylbenzonitrile has been described as a model compound for studying hydrogen bond formation in multifunctional molecules, as it contains four hydrogen bonding sites of which three are π-acceptors.

4-Ethynylbenzonitrile is a useful research compound. Its molecular formula is C9H5N and its molecular weight is 127.14 g/mol. The purity is usually 95%., 3032-92-6.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts