Day: November 1, 2021

COA of Formula: C8H7NO3. Sun, YL; Lu, CR; Zhao, B; Xue, MQ in [Lu, Chengrong; Zhao, Bei] Soochow Univ, Key Lab Organ Synth Jiangsu Prov, Suzhou 215123, Peoples R China; [Sun, Yuli; Lu, Chengrong; Zhao, Bei; Xue, Mingqiang] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China published Enantioselective Hydroboration of Ketones Catalyzed by Rare-Earth Metal Complexes Containing Trost Ligands in 2020.0, Cited 74.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

Four chiral dinuclear rare-earth metal complexes [REL1](2) (RE = Y(1), Eu(2), Nd(3), La (4)) stabilized by Trost proligand H3L1 (H3L1 = ( S,S) -2, 6-b is [2- (hydroxydiph enylmethyl)pyrrolidin-1-ylmethyl]-4-methyl-phenol) were first prepared, and all were characterized by X-ray diffraction. Complex 4 was employed as the catalyst for enantioselective hydroboration reaction of substituted ketones, and the corresponding secondary alcohols with excellent yields and high ee values were obtained using reductant HBpin. The same result was also achieved using the combination of lanthanium amides La[N(SiMe3)(2)](3) with Trost proligand H3L1 in a 1:1 molar ratio. The experimental findings and DFT calculation revealed the possible mechanism of the enantioselective hydroboration reaction and defined the origin of the enantioselectivity in the current system.

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Sun, YL; Lu, CR; Zhao, B; Xue, MQ or concate me.. COA of Formula: C8H7NO3

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Application In Synthesis of 2,2-Diphenylacetonitrile. Recently I am researching about PALLADIUM-CATALYZED 1,4-DIFUNCTIONALIZATION; LIGHT PHOTOREDOX CATALYSIS; CROSS-COUPLING REACTIONS; CARBON BOND FORMATION; DOMINO REACTIONS; HECK REACTION; C-C; CONJUGATED DIENES; ATOM-TRANSFER; HALIDES, Saw an article supported by the Alexander von Humboldt FoundationAlexander von Humboldt Foundation; Deutsche Forschungsgemeinschaft (Leibniz Award)German Research Foundation (DFG) [SBF 858]. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Huang, HM; Bellotti, P; Pfluger, PM; Schwarz, JL; Heidrich, B; Glorius, F. The CAS is 86-29-3. Through research, I have a further understanding and discovery of 2,2-Diphenylacetonitrile

Developing efficient and selective strategies to approach complex architectures containing (multi)stereogenic centers has been a long-standing synthetic challenge in both academia and industry. Catalytic cascade reactions represent a powerful means of rapidly leveraging molecular complexity from simple feedstocks. Unfortunately, carrying out cascade Heck-type reactions involving unactivated (tertiary) alkyl halides remains an unmet challenge owing to unavoidable beta-hydride elimination. Herein, we show that a modular, practical, and general palladium-catalyzed, radical three-component coupling can indeed overcome the aforementioned limitations through an interrupted Heck/allylic substitution sequence mediated by visible light. Selective 1,4-difunctionalization of unactivated 1,3-dienes, such as butadiene, has been achieved by employing different commercially available nitrogen-, oxygen-, sulfur-, or carbon-based nucleophiles and unactivated alkyl bromides (>130 examples, mostly >95:5 E/Z, >20:1 a). Sequential C(sp(3))-C(sp(3)) and C-X (N, O, S) bonds have been constructed efficiently with a broad scope and high functional group tolerance. The flexibility and versatility of the strategy have been illustrated in a gram-scale reaction and streamlined syntheses of complex ether, sulfone, and tertiary amine products, some of which would be difficult to access via currently established methods.

About 2,2-Diphenylacetonitrile, If you have any questions, you can contact Huang, HM; Bellotti, P; Pfluger, PM; Schwarz, JL; Heidrich, B; Glorius, F or concate me.. Application In Synthesis of 2,2-Diphenylacetonitrile

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Recently I am researching about TOSYLHYDRAZONES; FLUORINE; CONSTRUCTION; IMIDAZOLES; ALKYLATION; PYRAZOLES; UNIQUE, Saw an article supported by the National Key Research and Development Program of China [2016YFA0602900]; National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21420102003]; Guangdong Province Science FoundationNational Natural Science Foundation of Guangdong Province [2017B090903003]. Computed Properties of C8H7NO3. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Huang, YB; Lin, ZM; Chen, Y; Fang, SJ; Jiang, HF; Wu, WQ. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

Herein a novel and practical protocol to synthesize a series of N-difluoromethyl hydrazones via base-promoted N-difluoromethylation is reported. With hydrazones as chain substrates containing N-N bonds and TMSCF2Br as the difluoromethylation reagent, the reaction delivers N-difluoromethyl hydrazones in good yields, which exhibit good functional group tolerance and stereoselectivity.

Computed Properties of C8H7NO3. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Huang, YB; Lin, ZM; Chen, Y; Fang, SJ; Jiang, HF; Wu, WQ or concate me.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Recently I am researching about H BOND ACTIVATION; SELECTIVE CATALYTIC-HYDROGENATION; HEXAHYDRIDE COMPLEX; LIGANDS PREPARATION; N-H; DEHYDROGENATION; HYDRIDE; VINYLIDENE; RUTHENIUM; REACTIVITY, Saw an article supported by the MINECO of Spain [CTQ2017-82935-P, RED2018-102387-T]; Gobierno de AragonGobierno de Aragon [E06_20R, LMP148_18]; FEDEREuropean Commission; European Social FundEuropean Social Fund (ESF). Category: benzodioxans. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Babon, JC; Esteruelas, MA; Lopez, AM; Onate, E. The CAS is 86-29-3. Through research, I have a further understanding and discovery of 2,2-Diphenylacetonitrile

The transformation of alkyl nitriles to symmetrical and asymmetrical secondary aliphatic amines promoted by the hexahydride complex OsH6 ((PPr3)-Pr-i)(2) (1) is described, and the mechanisms of the reactions involved are established. Complex 1 catalyzes the aforementioned transformations of aryl-, pyridyl-, and alkoxy-functionalized alkyl nitriles with linear or branched chains. The formation of the secondary amines involves primary imines, primary amines, and secondary imines as organic intermediates. The reactions take place under mild conditions (toluene, 100 degrees C, and 4 bar of H-2). Stoichiometric reactions of 1 with pivalonitrile and 2-methoxyacetonitrile have allowed us to isolate the trihydride azavinylidene derivatives OsH3{=N=CHR}((PPr3)-Pr-i)(2) (R = Bu-t (3), CH2OMe (4)). Their formation involves the insertion of the N-C triple bond of the substrates into an Os-H bond of the unsaturated tetrahydride OsH4 ((PPr3)-Pr-i)(2) (A), which is generated by reductive elimination of H-2 from the hexahydride precursor. The reaction of these trihydride azavinylidene species with H-2 is the key step for the reduction of the N-C triple bond of the nitriles. In the absence of H-2, the attack of A to the azavinylidene ligand produces the rupture of its C(sp(2))-C(sp(3)) bond. As a consequence of this attack and the presence of primary imines and amines in the reaction media, the binuclear complexes ((PPr3)-Pr-i)(2) H4Os(mu-CN)OsH3{kappa(1)-N-(NH= CHCH2OMe)}((PPr3)-Pr-i)(2) (5) and ((PPr3)-Pr-i)(2)H4Os(mu-CN)OsH3{kappa(1)-N-(NH2CH2CH2OMe)}((PPr3)-Pr-i)(2) (6) have been isolated and characterized by X-ray diffraction analysis, for 2-methoxyacetonitrile. DFT calculations reveal noticeable similarities between the hydrogenations of nitriles to primary imines and those of primary imines to primary amines.

Category: benzodioxans. About 2,2-Diphenylacetonitrile, If you have any questions, you can contact Babon, JC; Esteruelas, MA; Lopez, AM; Onate, E or concate me.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Product Details of 100-19-6. In 2019.0 TETRAHEDRON LETT published article about FURAZAN DERIVATIVES; FUNCTIONALIZATION; MECHANISM; C-60 in [Gu, Zhen-Zhen; Guo, Feng-Chao; Zhang, Pu; Qin, Yu-Jun; Guo, Zhi-Xin] Renmin Univ China, Dept Chem, Beijing 100872, Peoples R China in 2019.0, Cited 36.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

Acetophenones with a variety of substituents could be converted to diacylfuroxans in a solvent-free reaction by combining the reagents Fe(NO3)(3)center dot 9H(2)O and P2O5 under high-speed ball milling. This reaction was facile and eco-friendly, and exhibits advantages in terms of better toleration, safety, and easier operation. The nitrate acid and nitrogen dioxide generated in situ should play a major role in this mechanochemical reaction. (C) 2019 Elsevier Ltd. All rights reserved.

Product Details of 100-19-6. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Gu, ZZ; Guo, FC; Zhang, P; Qin, YJ; Guo, ZX or concate me.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

I found the field of Pharmacology & Pharmacy very interesting. Saw the article Synthesis and Investigation on the Antidiabetic Effect of 3-aryl-1-(5-methylisox azol-3-ylamino)-1-(4-nitrophenyl) Propan-1-one published in 2019.0. COA of Formula: C8H7NO3, Reprint Addresses Yang, DC (corresponding author), Southwest Univ, Sch Chem & Chem Engn, Chongqing 400715, Peoples R China.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

Background: Diabetes mellitus is the third-largest non-communicable chronic disease worldwide. There are many effective drugs, but the long-term use of these clinical drugs may cause various side effects. Therefore, it is urgent to develop new antidiabetic molecules with higher efficacy and lower toxicity. Methods: Fifteen new 3-aryl-1-(5-methylisoxazol-3-ylamino)-1-(4-nitrophenyl)propan-1-one were synthesized directly through the Mannich reaction of 4-nitroacetophenone, 3-amino-5-methylisoxazole and aromatic aldehydes catalyzed by concentrated hydrochloric acid. The molecular structures of the products were fully characterized by H-1 NMR, C-13 NMR, ESI MS and HRMS. The peroxisome proliferator-activated receptor (PPAR) response element and alpha-glucosidase inhibitory activity of these compounds were evaluated in vitro. Molecular docking, molecular physical parameters calculation, and molecular toxicity prediction were performed to analyze the structure-activity relationship and evaluate the druggability of these compounds theoretically. Results: All compounds exhibited weak antidiabetic activities, but compound 15 showed promising as a high performance, dual-target antidiabetic lead compound with peroxisome proliferator-activated receptor (PPAR) response element relative agonist activity of 99.55% at 27.2 nmol.ml(-1) and alpha-glucosidase inhibitory activity of 35.21% at 13.6 nmol.mL(-1). All compounds obtained may have no cardiotoxicity, no acute toxicity, no carcinogenic, and within safe range of mutagenic risk. Conclusion: This study identified a potential PPAR lead molecule and presented an unusual strategy for antidiabetic drug development.

COA of Formula: C8H7NO3. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Liu, JY; Zhou, ZW; Liu, J; Yan, JF; Fan, L; Tang, XM; Liu, J; Chen, FF; Yang, DC or concate me.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

HPLC of Formula: C8H7NO3. I found the field of Chemistry very interesting. Saw the article Enantioselective Reduction of alpha,beta-Unsaturated Ketones and Aryl Ketones by Perakine Reductase published in 2019.0, Reprint Addresses Sun, LL (corresponding author), Zhejiang Univ, Coll Pharmaceut Sci, Inst Drug Metab & Pharmaceut Anal, Hangzhou 310058, Zhejiang, Peoples R China.; Zhao, JH (corresponding author), Zhejiang Univ, Inst Pesticide & Environm Toxicol, Minist Agr, Key Lab Mol Biol Crop Pathogens & Insects, Hangzhou 310029, Zhejiang, Peoples R China.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone.

This report describes the enantioselective reduction of structurally diverse alpha,beta-unsaturated ketones and aryl ketones by perakine reductase (PR) from Rauvolfia. This enzymatic reduction produces alpha-chiral allylic and aryl alcohols with excellent enantioselectivity and most of the products in satisfactory yields. Furthermore, the work demonstrates 1 mmol scale reactions for product delivery without any detrimental effect on yield and enantioselectivity. The catalytic mechanism, determined by 3D-structure-based modeling of PR and ligand complexes, is also described.

HPLC of Formula: C8H7NO3. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Cai, S; Shao, NN; Chen, YY; Li, AB; Pan, J; Zhu, HJ; Zou, HB; Zeng, S; Sun, LL; Zhao, JH or concate me.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

I found the field of Science & Technology – Other Topics very interesting. Saw the article Preparation of palladated porous nitrogen-doped carbon using halloysite as porogen: disclosing its utility as a hydrogenation catalyst published in 2020.0. Quality Control of 1-(4-Nitrophenyl)ethanone, Reprint Addresses Sadjadi, S (corresponding author), Iran Polymer & Petrochem Inst, Fac Petrochem, Gas Convers Dept, POB 14975-112, Tehran, Iran.; Heravi, MM (corresponding author), Alzahra Univ, Sch Sci, Dept Chem, POB 1993891176, Tehran, Iran.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

In this article, halloysite nanoclay (Hal) was used as porogen for the synthesis of nitrogen doped porous carbon material with high specific surface area and pore volume. To this purpose, polymerization of melamine and terephthalaldehyde (MT) was performed in the presence of amine-functionalized carbon coated Hal (Hal@Glu-2N) that was prepared from hydrothermal treatment of Hal and glucose. Then, the prepared nanocomposite was palladated and carbonized to afford Pd@Hal@C. To further improve the textural properties of the nanocomposite, and introduce more pores in its structure, Hal nanotubes were etched. The characterization of the resulting compound, Pd@C, and comparing it with Pd@Hal@C, showed that etching of Hal significantly increased the specific surface area and pore volume in Pd@C. Pd@C was successfully used as a heterogeneous catalyst for promoting hydrogenation of nitroarens in aqueous media using hydrogen with atmospheric pressure as a reducing agent. The comparison of the structural features and catalytic activity of the catalyst with some control catalysts, including, Pd@Hal, Pd@Hal@Glu, Pd@Hal@Glu-MT and Pd@Hal@C confirmed that nitrogen groups in C could improve the Pd anchoring and suppress its leaching, while etching of Hal and introduction of more pores could enhance the catalytic activity through facilitating the mass transfer.

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Sadjadi, S; Malmir, M; Lazzara, G; Cavallaro, G; Heravi, MM or concate me.. Quality Control of 1-(4-Nitrophenyl)ethanone

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

In 2020.0 EUR J ORG CHEM published article about SELECTIVE SYNTHESIS; PENTAARYLPYRIDINES; ARYLPYRIDINES; CONSTRUCTION; CONDENSATION; DERIVATIVES; ENAMINES; KINETICS; BINDING in [Arita, Mao; Yokoyama, Soichi; Asahara, Haruyasu; Nishiwaki, Nagatoshi] Kochi Univ Technol, Sch Environm Sci & Engn, Kami Kochi 7828502, Japan; [Yokoyama, Soichi; Asahara, Haruyasu; Nishiwaki, Nagatoshi] Kochi Univ Technol, Res Ctr Mat Sci & Engn, Kami Kochi 7828502, Japan; [Asahara, Haruyasu] Osaka Univ, Grad Sch Pharmaceut Sci, Yamadaoka 1-6, Suita, Osaka 5650871, Japan in 2020.0, Cited 47.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Recommanded Product: 1-(4-Nitrophenyl)ethanone

Condensation of beta-(2-pyridyl)enamine and alpha,beta-unsaturated ketone in the presence of FeCl3 under air afforded highly substituted pyridines. In this transformation, FeCl3 acted as not only an acid catalyst but also an oxidant for the intermediate dihydropyridine. The substituents could be easily modified by altering the substrates to obtain tri- and tetraarylpyridines including bipyridines and terpyridine. Synthesis of differently substituted pentaarylpyridines was consequently achieved via only three steps from commercially available reagents with simple experimental manipulations.

Recommanded Product: 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Arita, M; Yokoyama, S; Asahara, H; Nishiwaki, N or concate me.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

I found the field of Chemistry; Science & Technology – Other Topics very interesting. Saw the article HCl center dot DMPU-assisted one-pot and metal-free conversion of aldehydes to nitriles published in 2020. HPLC of Formula: C14H11N, Reprint Addresses Hammond, GB (corresponding author), Univ Louisville, Dept Chem, Louisville, KY 40292 USA.. The CAS is 86-29-3. Through research, I have a further understanding and discovery of 2,2-Diphenylacetonitrile

We report an efficient HCl center dot DMPU assisted one-pot conversion of aldehydes into nitriles. The use of HCl center dot DMPU as both an acidic source as well as a non-nucleophilic base constitutes an environmentally mild alternative for the preparation of nitriles. Our protocol proceeds smoothly without the use of toxic reagents and metal catalysts. Diverse functionalized aromatic, aliphatic and allylic aldehydes incorporating various functional groups were successfully converted to nitriles in excellent to quantitative yields. This protocol is characterized by a broad substrate scope, mild reaction conditions, and high scalability.

About 2,2-Diphenylacetonitrile, If you have any questions, you can contact Mudshinge, SR; Potnis, CS; Xu, B; Hammond, GB or concate me.. HPLC of Formula: C14H11N

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem