Category: 31643-49-9

Inorganic compounds containing the −C≡N group are not called nitriles, but cyanides instead.31643-49-9, formula is C8H3N3O2, Name is 4-Nitrophthalonitrile. Though both nitriles and cyanides can be derived from cyanide salts, most nitriles are not nearly as toxic. Computed Properties of 31643-49-9.

Botnar, A. A.;Domareva, N. P.;Kazaryan, K. Yu.;Tikhomirova, T. V.;Abramova, M. B.;Vashurin, A. S. research published 《 Synthesis and spectral properties of tetraphenoxy substituted erbium phthalocyanines containing peripheral phenyl and cyclohexyl fragments》, the research content is summarized as follows. The synthesis of peripherally and non-peripherally substituted erbium phthalocyanines with cyclohexylphenoxyl or phenylphenoxyl fragments by the template condensation of substituted phthalonitrile and erbium chloride in boiling isoamyl alc. was studied. The role of the influence of the substituents in the macrocycle on the yield of the product was revealed. The change in the spectra of the synthesized compounds in various solvents was studied.

Computed Properties 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

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. COA of Formula: C8H3N3O2.

Botnar, Anna;Tikhomirova, Tatiyana;Kazaryan, Kristina;Bychkova, Anna;Maizlish, Vladimir;Abramov, Igor;Vashurin, Artur research published 《 Synthesis and properties of tetrasubstituted phthalocyanines containing cyclohexylphenoxy-groups on the periphery》, the research content is summarized as follows. The data on synthesis and spectroscopic-luminescent proportion of novel peripheral and non-peripheral substituted cyclohexylphenoxy-phthalocyanine derivatives and their metal complexes with magnesium and zinc are given in the work. By means of the nucleophilic substitution reaction of 3- or 4-nitrophthalonitrile and 4-cyclohexylphenol, the 3/4-(4-cyclohexylphenoxy)phthalonitriles were synthesized and further characterized by ¹H NMR, IR spectroscopy and elemental anal. Metal complexes synthesis were carried out by template fusion of substituted nitriles with appropriate metal acetates, whereas the ligands were obtained through demetallization of magnesium complexes in hydrochloric acid. It was found non-peripheral substituted magnesium and zinc complexes in the chloroform and toluene solutions forms J-type aggregates. Peripheral substituted metal complexes possess more pronounced fluorescent properties compare to non-peripheral ones.

COA of Formula: C8H3N3O2, 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

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). 31643-49-9, formula is C8H3N3O2, Name is 4-Nitrophthalonitrile. 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. Product Details of C8H3N3O2.

Butler, Tristan;Bunton, Caleb;Ryou, Heonjune;Dyatkin, Boris;Weise, Nickolaus;Laskoski, Matthew research published 《 Influence of molecular weight on thermal and mechanical properties of bisphenol A-based phthalonitrile resins》, the research content is summarized as follows. This effort assesses the correlation between chem. structures and performance-essential thermal, mech., and long-term stability properties of cross-linked thermosets. Resins of different mol. weights were prepared from the Bisphenol A based PEEK-like oligomeric phthalonitrile (BisA). Differential scanning calorimetry, which was used to investigate curing thermodn., indicated that BisA resins demonstrated pos. correlation between increasing oligomer mol. weight and both resulting m.ps. and cure initiation conditions. Characterization of thermal properties using thermogravimetric anal. (TGA) indicated a similar mol. weight trend, with char yields ranging between 57% and 73%. Rheol. studies of BisA of different mol. weights indicated significant viscosity increases in phthalonitriles that crosslinked from oligomers with higher mol. weights Moreover, the n = 1 chain length resin exhibited a gel point at 100°C lower than the n = 25 oligomer. Anal. of hardness of these cured polymers indicated that the resin crosslinked using the n = 1 oligomer was most brittle, while the thermoset derived from the n = 4 BisA demonstrated highest hardness. Aging of cured phthalonitriles indicated that the n = 10 remained most stable in long-duration high-temperature environments. This study suggests the use of preparing BisA thermosets from oligomers with different mol. weights as an effective strategy for improving toughness, albeit at the tradeoff of lower thermal stabilities.

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., Product Details of C8H3N3O2

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). 31643-49-9, formula is C8H3N3O2, Name is 4-Nitrophthalonitrile. 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. HPLC of Formula: 31643-49-9.

Cavus, Aleyna;Gork, Gulsen;Erdem, Murat;Ozer, Metin research published 《 Synthesis and characterization of the novel 4-(1-(pyridin-4-yl) ethoxyl) substituted bis(phthalocyaninato) rare earth complexes and investigation of their two-photon absorption-based third-order non-linear optical properties》, the research content is summarized as follows. Novel 4-(1-(pyridin-4-yl) ethoxyl) substituted double-decker rare earth phthalocyanine complexes were synthesized starting from (R)-4-(1-(pyridin-4-yl) ethoxy) phthalonitrile with proper rare earth metal acetates in octanol catalyzed by 1,8-diazabicyclo[5.4.0]undec-7-ene at 300°C. The new starting phthalonitrile compound was obtained from (R)-1-(pyridin-4-yl) ethan-1-ol and 4-nitrophthalonitrile in acetonitrile at reflux temperature in the presence of potassium carbonate as a catalyst. The characterization of the synthesized and isolated compounds was performed by elemental anal., IR, UV-visible, proton and correlation spectroscopy NMR, and matrix-assisted laser desorption/ionization time-of-flight mass spectroscopic methods. Nonlinear optical responses of all complexes are investigated using the Z-scan method. The nonlinear absorption coefficient, two-photon absorption cross-section, and the imaginary part of the nonlinear susceptibility of complexes are calculated for each discrete concentration All these nonlinear parameters of our rare-earth coordinated double-decker phthalocyanines present a decrement due to the aggregation under high optic powers, which result in sequential two-photon absorption for smaller ionic radii.

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., HPLC of Formula: 31643-49-9

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. Category: nitriles-buliding-blocks.

Demirbas, Umit;Ozturk, Dilek;Akcay, Hakki Turker;Durmus, Mahmut;Mentese, Emre;Kantekin, Halit research published 《 Metallo-phthalocyanines containing triazole substituents: Synthesis, spectroscopic and photophysicochemical properties》, the research content is summarized as follows. Magnesium(II) (4), lead(II) (5) and zinc(II) (6) phthalocyanines were prepared The structures of 4–6 were confirmed by the spectroscopic characterization such as FTIR, ¹H-NMR, MALDI-TOF mass, UV-visible and fluorescence spectral data. The aggregation behavior of the triazole substituted phthalocyanines (4–6) was studied in different solvents and no aggregation was observed The photophysicochem. properties of 4–6 were studied in DMSO. The photophys. and photochem. behaviors varied depending on the type of metal in the center of phthalocyanine. The zinc(II) phthalocyanine 6 showed the highest singlet oxygen quantum yield and the highest photostability. The magnesium(II) phthalocyanine 4 exhibited the highest fluorescence quantum yield. The zinc(II) phthalocyanine 6 has good photosensitizer performance due to its high singlet oxygen generation ability, high photostability and formation of non-aggregated species.

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., Category: nitriles-buliding-blocks

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Inorganic compounds containing the −C≡N group are not called nitriles, but cyanides instead.31643-49-9, formula is C8H3N3O2, Name is 4-Nitrophthalonitrile. Though both nitriles and cyanides can be derived from cyanide salts, most nitriles are not nearly as toxic. Application of C8H3N3O2.

He, Liang;Tong, Lifen;Xia, Yunqing;Lin, Guo;Wang, Ting;Zhang, Wanru;Liu, Yingfa;Liu, Xiaobo research published 《 Advanced composites based on end-capped polyarylene ether nitrile/bisphthalonitrile with controllable thermal curing reaction》, the research content is summarized as follows. A novel polymer was prepared through the combination of phthalonitrile end-capped polyarylene ether nitrile (PEN-Ph) and bisphthalonitrile (BPh), applying post-solid phase chem. reaction technol. BPh monomer was firstly pre-polymerized to form BPh prepolymer and then followed by crosslinking reaction with PEN-Ph matrix resin to obtain PEN-Ph/BPh composites. The generated crosslinking structures were confirmed by FTIR and UV including phthalocyanine, triazine, and isoindoline rings. Besides, the effect of BPh pre-polymerization time on the performance of PEN-Ph/BPh composite materials was studied. Tensile strength and modulus highest values of composites exceeded 98.9 MPa and 2.17 GPa resp. as BPh pre-polymerization time reached 30 min, improved by 55.6% and 36.9% in comparison with unpolymerized one. Besides, PEN-Ph/BPh composite films exhibited superior thermal properties (T_g: 278-330°C, T_5% (decomposition temperature of 5 wt%)>500°C) and maintained excellent dielec. stability over 300°C, leading to use for electronic fields at elevated temperature

Application of C8H3N3O2, 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

Inorganic compounds containing the −C≡N group are not called nitriles, but cyanides instead.31643-49-9, formula is C8H3N3O2, Name is 4-Nitrophthalonitrile. Though both nitriles and cyanides can be derived from cyanide salts, most nitriles are not nearly as toxic. Recommanded Product: 4-Nitrophthalonitrile.

Demirbas, Umit;Yanik, Hulya;Akcay, Hakki Turker;Durmus, Mahmut;Bekircan, Olcay;Kantekin, Halit research published 《 Synthesis, characterization, photophysical and photochemical properties of peripherally tetra-1,2,4-triazol-3-ylthio substituted metal-free phthalocyanine and its zinc(II) and lead(II) derivatives》, the research content is summarized as follows. Phthalonitrile (3) including 4-(4-fluorophenyl)-5-(4-methoxyphenyl)-4H-1,2,4-triazole-3-thio substituent and its peripherally tetra substituted metal-free (4), zinc(II) (5) and lead(II) (6) phthalocyanine derivatives were prepared and characterized by FTIR, mass, ¹HNMR and ¹³CNMR spectroscopic data. All studied phthalocyanines had good solubility in common organic solvents and did not aggregate. The photophys. and photochem. behaviors of the phthalocyanine complexes (4–6) were examined in DMSO to determinate their PDT potential. Singlet oxygen, fluorescence and photodegradation quantum yields showed that zinc(II) phthalocyanine (5) has potential as Type II photosensitizer for PDT applications.

Recommanded Product: 4-Nitrophthalonitrile, 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

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). 31643-49-9, formula is C8H3N3O2, Name is 4-Nitrophthalonitrile. 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. Application of C8H3N3O2.

He, Liang;Tong, Lifen;Bai, Zhongxiang;Lin, Guo;Xia, Yunqing;Liu, Xiaobo research published 《 Investigation of the controllable thermal curing reaction for ultrahigh T_g polyarylene ether nitrile compositions》, the research content is summarized as follows. High-performance polymer plays critical roles in 5G communication and electronic applications. Hence, special engineering plastic polyarylene ether nitrile (PEN) suitable for use in a harsh environment (T_g > 400°C,T_5% > 500°C, and tensile strength 100 MPa) has been developed. Bisphthalonitrile (BPh) units form a flexible bridge between the nitrile of PEN. In the preparation, DDS acts as a catalyst and ZnCl₂ functions as both a catalyst and a reinforcing phase, to enhance the degree of crosslinking and mech. properties of the resulting compositions Therefore, the structure of a linear polymer is converted into a 3D network, resulting in greatly enhanced performance. The mode of action for DDS/ZnCl₂ and the transformation of nitrile groups has been described. These insights provide an understanding of the impact of crosslinking factors in structure formation and supply a feasible design strategy for the preparation of high-performance polymer films.

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., Application of C8H3N3O2

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). 31643-49-9, formula is C8H3N3O2, Name is 4-Nitrophthalonitrile. 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. Recommanded Product: 4-Nitrophthalonitrile.

Agcaabat, Ruveyda;Bilen Senturk, Cansu;Odabas, Zafer research published 《 The effect of the position of the trimethoxy groups as distant substituents on the spectral and acid sensing properties of phthalocyanines》, the research content is summarized as follows. In this study, alpha and beta substituted phthalonitrile derivatives were obtained by using 3,4,5-trimethoxyphenol and 2,4,6-trimethoxyphenol, and metal-free and Co²⁺ phthalocyanine mols. were synthesized using these starting compounds After the phthalocyanine compounds were purified and characterized by classical methods, their detailed solubility, UV-Vis and FT-IR spectroscopy studies were performed and it was revealed how the positions of methoxy groups changed the spectroscopic properties of phthalocyanines. In addition, during detailed UV-Vis studies of Pcs, it was determined that alpha-substituted Pcs gave an extra peak in 1 x 10^-5 M dichloromethane solution It was determined that this peak was caused by acid impurities in dichloromethane in trace amounts and UV-Vis spectra in DCM solutions with different trifluoroacetic acid(TFA) concentrations for alpha substituted Pcs (5–8) were studied and their protonation behavior was examined It was determined that H2Pc(6) was sensitive to acid even at 1.8 x 10^-3 mM concentration Thus, acid sensor device can be developed by using this Pc mol., if desired.

Recommanded Product: 4-Nitrophthalonitrile, 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

Inorganic compounds containing the −C≡N group are not called nitriles, but cyanides instead.31643-49-9, formula is C8H3N3O2, Name is 4-Nitrophthalonitrile. Though both nitriles and cyanides can be derived from cyanide salts, most nitriles are not nearly as toxic. Quality Control of 31643-49-9.

Agirtas, Mehmet Salih;Solgun, Derya Gungordu;Yildiko, Umit research published 《 Synthesis, theoretical DFT analysis, photophysical and photochemical properties of a new zinc phthalocyanine compound》, the research content is summarized as follows. In this study, fluorescent zinc phthalocyanine compound was synthesized using 4-(2-(4-(2-phenylpropan-2-yl) phenoxy) phenoxy) phthalonitrile and zinc metal salt. The structure of compounds was characterized by using 1H, and 13C NMR, FT-IR, Mass, UV-Vis spectroscopy. The fluorescence emission, excitation and absorption properties of this phthalocyanine compound were studied in THF and DMSO. Aggregation behaviors for different concentrations in the same solvent were investigated. Quantum chem. calculations were performed using 6-311G basis set of DFT (B3LYP and CAMB3LYP) methods. The structural optimization, MO anal., and electronic properties of the synthesized phthalocyanine were then determined in the ground state and gas phase of the DFT method. Moreover, mol. electrostatic potential (MEP) maps were drawn to identify the reactive regions of the zinc phthalocyanine complex. The data of the study show that the phthalocyanine complex can be used as sensor agent for biol. fluorescence anal.

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., Quality Control of 31643-49-9

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts