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N-(3-(trifluoromethyl)phenyl)benzo[d]oxazol-2-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39190-20-0

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39190-20-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39190-20-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,1,9 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 39190-20:
(7*3)+(6*9)+(5*1)+(4*9)+(3*0)+(2*2)+(1*0)=120
120 % 10 = 0
So 39190-20-0 is a valid CAS Registry Number.

39190-20-0Downstream Products

39190-20-0Relevant academic research and scientific papers

Synthesis, biological evaluation and molecular docking study of N-arylbenzo[d]oxazol-2-amines as potential α-glucosidase inhibitors

Wang, Guangcheng,Peng, Zhiyun,Wang, Jing,Li, Juan,Li, Xin

, p. 5374 - 5379 (2016)

A novel series of N-arylbenzo[d]oxazol-2-amines (4a–4m) were synthesized and evaluated for their α-glucosidase inhibitory activity. Compounds 4f–4i, 4k and 4m displayed potent inhibitory activity against α-glucosidase with IC50values in the range of 32.49?±?0.17–120.24?±?0.51?μM as compared to the standard drug acarbose. Among all tested compounds, compound 4g having 4-phenoxy substitution at the phenyl ring was found to be the most active inhibitor of α-glucosidase with an IC50value of 32.49?±?0.17?μM. Analysis of the kinetics of enzyme inhibition indicated that compound 4g is a noncompetitive inhibitor of α-glucosidase with a Kivalue of 31.33?μM. Binding interaction of compound 4g with α-glucosidase was explored by molecular docking simulation.

Synthesis of N-aryl-2-aminobenzoxazoles from substituted benzoxazole-2-thiol and 2-chloro-N-arylacetamides in KOH-DMF system

Wang, Guang-Cheng,Wang, Jing,Li, Lu-Yao,Chen, Shan,Peng, Ya-Ping,Xie, Zhen-Zhen,Chen, Ming,Deng, Bin,Li, Wen-Biao

, p. 1257 - 1268 (2017/07/18)

A simple and novel method for the synthesis of N-aryl-2-aminobenzoxazoles from substituted benzoxazole-2-thiol and 2-chloro-N-arylacetamides in KOH-DMF system has been developed. The present protocol provides an attractive approach to access various N-aryl-2-aminobenzoxazoles in moderate to good yields without using transition metal catalyst under very mild reaction condition.

Substituted 2-anilinobenzoxazoles

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, (2008/06/13)

Compositions comprising certain 2-(substituted anilino)benzoxazoles, such as 2-[4-bromo-3-(trifluoromethyl)-anilino]benzoxazole, and methods for using same as immunosuppressive agents, antifertility agents, for the prophylaxis of Marek's disease in chicke

Substituted 2-anilinobenzoxazoles used as immunosuppressive agents

-

, (2008/06/13)

Compositions comprising certain 2-(substituted anilino)benzoxazoles, such as 2-[4-bromo-3-(trifluoromethyl)anilino]benzoxazole, and methods for using same as immunosuppressive agents, antifertility agents, for the prophylaxis of Marek's disease in chicken

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