Tag: M.W=100-150

McEwen, Charles N. published the artcileSublimation Driven Ionization for Use in Mass Spectrometry: Mechanistic Implications, Synthetic Route of 91-15-6, the main research area is mass spectrometry ionization sublimation driven.

Sublimation has been known at least since the middle ages. This process is frequently taught in schools through the use of phase diagrams. Astonishingly, such a well-known process appears to still harbor secrets. Under conditions in which compound sublimation occurs, gas-phase ions are frequently detected using mass spectrometry. This was exploited in matrix-assisted ionization in vacuum (vMAI) by adding analyte to subliming compounds used as matrixes. Good vMAI matrixes were those that ionize the added analyte with high sensitivity, but even matrixes that fail this test often produce ions of likely matrix impurities suggesting that they may be good matrixes for some compound types. We also show that binary matrixes may be manipulated to provide desired properties such as fast analyses and improved sensitivity. These results imply that sublimation in some cases is more complicated than just mols. leaving a surface and that understanding the phys. force responsible, and how the nonvolatile compound becomes charged, could lead to improved ionization efficiency for mass spectrometry. Here we provide insights into this process and an explanation of why this unexpected phenomenon has not previously been reported.

Journal of the American Society for Mass Spectrometry published new progress about Impurities. 91-15-6 belongs to class nitriles-buliding-blocks, name is Phthalonitrile, and the molecular formula is C8H4N2, Synthetic Route of 91-15-6.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Lee, Chuping published the artcileToward understanding the ionization mechanism of matrix-assisted ionization using mass spectrometry experiment and theory, Application In Synthesis of 91-15-6, the main research area is ionization mechanism MALDI mass spectrometry experiment theory.

Rationale : Matrix-assisted ionization (MAI) mass spectrometry does not require voltages, a laser beam, or added heat to initiate ionization, but it is strongly dependent on the choice of matrix and the vacuum conditions. High charge state distributions of nonvolatile analyte ions produced by MAI suggest that the ionization mechanism may be similar to that of electrospray ionization (ESI), but different from matrix-assisted laser desorption/ionization (MALDI). While significant information is available for MAI using mass spectrometers operating at atm. and intermediate pressure, little is known about the mechanism at high vacuum. Methods : Eleven MAI matrixes were studied on a high-vacuum time-of-flight (TOF) mass spectrometer using a 266. nm pulsed laser beam under otherwise typical MALDI conditions. Detailed comparisons with the commonly used MALDI matrixes and theor. prediction were made for 3-nitrobenzonitrile (3-NBN), which is the only MAI matrix that works well in high vacuum when irradiated with a laser. Results : Screening of MAI matrixes with good absorption at 266 nm but with various degrees of volatility and laser energies suggests that volatility and absorption at the laser wavelength may be necessary, but not sufficient, criteria to explain the formation of multiply charged analyte ions. 3-NBN produces intact, highly charged ions of nonvolatile analytes in high-vacuum TOF using a laser, demonstrating that ESI-like ions can be produced in high vacuum. Theor. calculations and mass spectra suggest that thermally induced proton transfer, which is the major ionization mechanism in MALDI, is not important with the 3-NBN matrix at 266 nm laser wavelength. 3-NBN:analyte crystal morphol. is, however, important in ion generation in high vacuum. Conclusions : The 3-NBN MAI matrix produces intact, highly charged ions of nonvolatile compounds in high-vacuum TOF mass spectrometers with the aid of ablation and/or heating by laser irradiation, and shows a different ionization mechanism from that of typical MALDI matrixes.

Rapid Communications in Mass Spectrometry published new progress about Ionization. 91-15-6 belongs to class nitriles-buliding-blocks, name is Phthalonitrile, and the molecular formula is C8H4N2, Application In Synthesis of 91-15-6.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Molaei, Somayeh published the artcileOrdered mesoporous SBA-15 functionalized with yttrium(III) and cerium(III) complexes: Towards active heterogeneous catalysts for oxidation of sulfides and preparation of 5-substituted 1H-tetrazoles, Safety of Phthalonitrile, the main research area is sulfoxide tetrazole preparation SBA 15 functionalized yttrium cerium complex; sulfide nitrile oxidation.

Mesoporous SBA-15 was synthesized and modified with 3-chloropropyltrimethoxysilane and then used in immobilization of creatinine groups, which were employed to introduce Y3+ and Ce3+ to give rise to two novel yttrium and cerium catalysts: SBA-15@Creatinine@M (M = Y and Ce). The structures of the SBA-15@Creatinine@M catalysts were determined using various techniques. These catalysts offered outstanding catalytic performances in the oxidation of sulfides to sulfoxides and in the preparation of 5-substituted 1H-tetrazoles. An important characteristic of the SBA-15@Creatinine@M catalysts is that they are very stable without a considerable decrease in their catalytic performance lasting seven cycles.

Applied Organometallic Chemistry published new progress about IR spectra. 91-15-6 belongs to class nitriles-buliding-blocks, name is Phthalonitrile, and the molecular formula is C8H4N2, Safety of Phthalonitrile.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Nakagawa, Masayuki published the artcilePhotonucleophilic reactions of nitrofen, Safety of 4-Hydroxyisophthalonitrile, the main research area is nitrofen photonucleophilic reaction; photolysis nitrofen.

Irradiation of nitrofen (I) [1836-75-5] in the presence of KCN formed 2,4-dichlorobenzonitrile [6574-98-7] and related compounds, whereas the photoreaction with piperidine formed p-nitrophenol [100-02-7] and tarry products from the addnl. reactions of the intermediate 2,4-dichlorophenol [120-83-2] with piperidine. 2,4-Dichlorophenol also reacted with KCN to form 2,4-dicyanophenol [34133-58-9]. These and other photonucleophilic reactions may help to explain the environmental dissipation of many pesticides.

Journal of Agricultural and Food Chemistry published new progress about Photolysis. 34133-58-9 belongs to class nitriles-buliding-blocks, name is 4-Hydroxyisophthalonitrile, and the molecular formula is C8H4N2O, Safety of 4-Hydroxyisophthalonitrile.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Kamiya, Yusuke published the artcilePrediction of permeability across intestinal cell monolayers for 219 disparate chemicals using in vitro experimental coefficients in a pH gradient system and in silico analyses by trivariate linear regressions and machine learning, Computed Properties of 91-15-6, the main research area is intestinal cell monolayer permeability silico TLR machine learning; Caco-2 cells; Machine learning; Multivariate analysis; Octanol–water distribution coefficient; Permeability.

For medicines, the apparent membrane permeability coefficients (Papp) across human colorectal carcinoma cell line (Caco-2) monolayers under a pH gradient generally correlate with the fraction absorbed after oral intake. Furthermore, the in vitro Papp values of 29 industrial chems. were found to have an inverse association with their reported no-observed effect levels for hepatotoxicity in rats. In the current study, we expanded our influx permeability predictions for the 90 previously investigated chems. to both influx and efflux permeability predictions for 207 diverse primary compounds, along with those for 23 secondary compounds Trivariate linear regression anal. found that the observed influx and efflux logPapp values determined by in vitro experiments significantly correlated with mol. weights and the octanol-water distribution coefficients at apical and basal pH levels (pH 6.0 and 7.4, resp.) (apical to basal, r = 0.76, n = 198; and basal to apical, r = 0.77, n = 202); the distribution coefficients were estimated in silico. Further, prediction accuracy was enhanced by applying a light gradient boosting machine learning system (LightGBM) to estimate influx and efflux logPapp values that incorporated 17 and 19 in silico chem. descriptors (r = 0.83-0.84, p < 0.001). The determination in vitro and/or prediction in silico of permeability coefficients across intestinal cell monolayers of a diverse range of industrial chems./food components/medicines could contribute to the safety evaluations of oral intakes of general chems. in humans. Such new alternative methods could also reduce the need for animal testing during toxicity assessment. Biochemical Pharmacology (Amsterdam, Netherlands) published new progress about Algorithm. 91-15-6 belongs to class nitriles-buliding-blocks, name is Phthalonitrile, and the molecular formula is C8H4N2, Computed Properties of 91-15-6.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Wimmer, Eric published the artcileAn autonomous self-optimizing flow machine for the synthesis of pyridine-oxazoline (PyOX) ligands, Recommanded Product: Picolinonitrile, the main research area is pyridine oxazoline ligand self optimizing flow machine.

Pyridine-oxazoline-type ligands (PyOX) are an important class of chiral ligands for metal-catalyzed asym. transformations. Herein we describe an efficient and reliable flow route which is amenable for the synthesis of PyOX ligands at a scale of hundreds of milligrams per h. Optimal flow conditions were rapidly identified through the assistance of an inhouse built autonomous self-optimizing system integrating a custom-made optimization algorithm derived from the Nelder-Mead and golden section search methods. The preparation of a small library of representative PyOX ligands highlights the practical application of this flow route which should be of primary interest for synthetic chemists developing metal-catalyzed asym. transformations.

Reaction Chemistry & Engineering published new progress about Algorithm. 100-70-9 belongs to class nitriles-buliding-blocks, name is Picolinonitrile, and the molecular formula is C6H4N2, Recommanded Product: Picolinonitrile.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Saul, Sirle published the artcileIdentification and evaluation of 4-anilinoquin(az)olines as potent inhibitors of both dengue virus (DENV) and Venezuelan equine encephalitis virus (VEEV), Safety of 2-Aminobenzonitrile(Flakes or Chunks), the main research area is anilinoquinoline anilinoquinazoline antiviral dengue virus Venezuelan equine encephalitis virus; Alphavirus; Antiviral; Dengue virus; Flavivirus; Venezuelan equine encephalitis virus.

There is an urgent need for novel strategies for the treatment of emerging arthropod-borne viral infections, including those caused by dengue virus (DENV) and Venezuelan equine encephalitis virus (VEEV). We prepared and screened focused libraries of 4-anilinoquinolines and 4-anilinoquinazolines for antiviral activity and identified three potent compounds N-(2,5-dimethoxyphenyl)-6-(trifluoromethyl)quinolin-4-amine (10, I) inhibited DENV infection with an EC50 = 0.25μM, N-(3,4-dichlorophenyl)-6-(trifluoromethyl)quinolin-4-amine (27, II) inhibited VEEV with an EC50 = 0.50μM, while N-(3-ethynyl-4-fluorophenyl)-6,7-dimethoxyquinazolin-4-amine (54, III) inhibited VEEV with an EC50 = 0.60μM. These series of compounds demonstrated nearly no toxicity with CC50 values greater than 10μM in all cases. These promising results provide a future prospective to develop a clin. compound against these emerging viral threats.

Bioorganic & Medicinal Chemistry Letters published new progress about Antiviral agents. 1885-29-6 belongs to class nitriles-buliding-blocks, name is 2-Aminobenzonitrile(Flakes or Chunks), and the molecular formula is C7H6N2, Safety of 2-Aminobenzonitrile(Flakes or Chunks).

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Wang, Zhaoyang published the artcileMechanisms and reaction conditions of CO2 with o-aminobenzonitrile for the synthesis of quinazoline-2,4-dione, Category: nitriles-buliding-blocks, the main research area is review carbon dioxide aminobenzonitrile quinazolinedione reaction condition.

Quinazoline-2,4(1H,3H)-dione derivatives are key intermediates in pharmaceutical, biol. and chem. fields. To avoid the use of toxic carbonylation reagents such as phosgene, carbon monoxide and potassium cyanate, green synthesis methods for preparing quinazolindiones via the reaction of o-aminobenzonitrile with CO2 are developed. In this review, the factors such as reaction medium, catalyst and reaction temperature that influence the reaction of o-aminobenzonitrile with CO2 are systematically discussed. The protic solvent is favorable for the nitrile group as the initial reaction site to react with CO2. In contrast, the reactivity of the nitrile group and amino group of o-aminobenzonitrile could hardly be affected by aprotic solvent. Moreover, the reaction is also strongly affected by the catalyst, which is evaluated by the basicity and nucleophilicity of the catalyst. Specifically, the basicity mainly affects the activation of the amino group in the o-aminobenzonitrile substrate, whereas the nucleophilicity primarily impacts the formation of the CO2 activated state. The similarities and differences of different catalysts such as organic bases, inorganic bases, ionic liquids and supported catalysts in specific reaction pathways are also discussed in this review. In addition, the formation of isocyanate intermediate in the rearrangement process is significantly affected by the reaction temperature The quinazolindione could be easily formed from the isocyanate intermediate, isomerized from the cyclic carbamate, under high reaction temperature Furthermore, the quinazolindione could be formed directly by the isomerized cyclic carbamate under low reaction temperature

Journal of CO2 Utilization published new progress about Aprotic solvents. 1885-29-6 belongs to class nitriles-buliding-blocks, name is 2-Aminobenzonitrile(Flakes or Chunks), and the molecular formula is C7H6N2, Category: nitriles-buliding-blocks.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Yang, Xulin published the artcileDesigning phthalonitrile/hydroxyl compound systems for high performance CFRP composites, HPLC of Formula: 91-15-6, the main research area is phthalonitrile hydroxyl compound system carbon fiber reinforced polymer composite.

High mech. residues at/after elevated temperatures are basic prerequisites for the engineering applications of carbon fiber reinforced polymer (CFRP) composites in special fields like aerospace. In this study, phthalonitrile (PNP) copolymers based on hydroxyl compounds of BP monomer, PEP and BZCN resin were designed and their curing behavior and processability were investigated for realizing the corresponding CFRP composites. High temperature mech. performances of PNP/hydroxyl compound/CF composites under instantaneous and non-instantaneous states are systematically assessed. At 300°C, PNP/hydroxyl compounds/CF composite showed a retention rate of tensile, compressive, flexural strength and flexural modulus higher than 35%, 95%, 80% and 90%, resp. After 300°C/50 h thermal aging, their flexural properties show no obvious attenuation. Even after being aged at 350°C for 50 h, the residue of flexural modulus is above 90% while that of flexural strength is over 60%. The mass residue of PNP/hydroxyl compounds/CF composites were all higher than 98% and 90% after aging at 300°C and 350°C for 50 h. PNP/hydroxyl compounds/CF composites, with the excellent comprehensive mech. properties, can be used as high performance engineering materials.

Materials Research Express published new progress about Bending strength. 91-15-6 belongs to class nitriles-buliding-blocks, name is Phthalonitrile, and the molecular formula is C8H4N2, HPLC of Formula: 91-15-6.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Yu, Bin published the artcileDesign, Synthesis, and Evaluation of the Antifungal Activity of Novel Pyrazole-Thiazole Carboxamides as Succinate Dehydrogenase Inhibitors, HPLC of Formula: 1885-29-6, the main research area is pyrazole thiazole carboxamide derivative preparation succinate dehydrogenase inhibitor antifungal; fungicidal activity; molecular docking; structure−activity relationships; succinate dehydrogenase inhibitors.

Succinate dehydrogenase (SDH) is regarded as a promising target for fungicide discovery. To continue our ongoing studies on the discovery of novel SDH inhibitors as fungicides, novel pyrazole-thiazole carboxamides were designed, synthesized, and evaluated for their antifungal activity. The results indicated that compounds 9ac, 9bf, and 9cb showed excellent in vitro activities against Rhizoctonia cerealis with EC50 values from 1.1 to 4.9 mg/L, superior to that of the com. fungicide thifluzamide (EC50 = 23.1 mg/L). Compound 9cd (EC50 = 0.8 mg/L) was far more active than thifluzamide (EC50 = 4.9 mg/L) against Sclerotinia sclerotiorum. Compound 9ac exhibited promising in vivo activity against Rhizoctonia solani (90% at 10 mg/L), which was better than that of thifluzamide (80% at 10 mg/L). The field experiment showed that compound 9ac had 74.4% efficacy against Rhizoctonia solani on the 15th day after two consecutive sprayings at an application rate of 4.80 g a.i./667 m2, which was close to that of thifluzamide (83.3%). Furthermore, mol. docking explained the possible binding mode of compound 9ac in the RcSDH active site. Our studies indicated that the pyrazole-thiazole carboxamide hybrid is a new scaffold of SDH inhibitors.

Journal of Agricultural and Food Chemistry published new progress about Botrytis cinerea. 1885-29-6 belongs to class nitriles-buliding-blocks, name is 2-Aminobenzonitrile(Flakes or Chunks), and the molecular formula is C7H6N2, HPLC of Formula: 1885-29-6.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts