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4-phenyl-2-Thiophenamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67637-83-6

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67637-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67637-83-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,6,3 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 67637-83:
(7*6)+(6*7)+(5*6)+(4*3)+(3*7)+(2*8)+(1*3)=166
166 % 10 = 6
So 67637-83-6 is a valid CAS Registry Number.

67637-83-6Relevant academic research and scientific papers

Discovery of novel N-(5-(arylcarbonyl)thiazol-2-yl)amides and N-(5-(arylcarbonyl)thiophen-2-yl)amides as potent RORγt inhibitors

Wang, Yonghui,Cai, Wei,Zhang, Guifeng,Yang, Ting,Liu, Qian,Cheng, Yaobang,Zhou, Ling,Ma, Yingli,Cheng, Ziqiang,Lu, Sijie,Zhao, Yong-Gang,Zhang, Wei,Xiang, Zhijun,Wang, Shuai,Yang, Liuqing,Wu, Qianqian,Orband-Miller, Lisa A.,Xu, Yan,Zhang, Jing,Gao, Ruina,Huxdorf, Melanie,Xiang, Jia-Ning,Zhong, Zhong,Elliott, John D.,Leung, Stewart,Lin, Xichen

, p. 692 - 702 (2014/01/23)

Novel series of N-(5-(arylcarbonyl)thiazol-2-yl)amides and N-(5-(arylcarbonyl)thiophen-2-yl)amides were discovered as potent retinoic acid receptor-related orphan receptor-gamma-t (RORγt) inhibitors. SAR studies of the RORγt HTS hit 6a led to identification of thiazole ketone amide 8h and thiophene ketone amide 9g with high binding affinity and inhibitory activity of Th17 cell differentiation. Compound 8h showed in vivo efficacy in both mouse experimental autoimmune encephalomyelitis (EAE) and collagen induced arthritis (CIA) models via oral administration.

RETINOID-RELATED ORPHAN RECEPTOR GAMMA MODULATORS, COMPOSITION CONTAINING THEM AND USES THEREOF

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Page/Page column 13, (2012/08/08)

Provided are retinoid-related orphan receptor gamma(ROR γ) modulators of formula (I), processes for their preparation, pharmaceutical compositions containing them, and their uses in the treatment of diseases mediated by ROR γ.

Reaction of 2-Thiophenamines with Hydrazine

Gewald, Karl,Hain, Ute,Gruner, Margit

, p. 573 - 576 (2007/10/02)

Depending on their substituents 2-thiophenamines react with hydrazine hydrate on different ways: Hydrazinolysis of the ester 1 yields the 2-amino-3-thiophenecarbohydrazide 2. 4-Phenyl-2-thiophenamine (4) is converted into the 2(5H)-thiophenone hydrazone 5 by exchange of the amino group.The thiophenamines 7, 9, 12 undergo ring transformation to yield pyridazine derivatives, the N,N'-bis(dihydro-3-pyridazinyl)hydrazine 8, the 3-pyridazinylhydrazine 10, and the pyrazolopyridazine 13.From 10 the 1,2,4-triazolopyridazine 11 is obtained.

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