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(1H-indol-3-yl)(4-(trifluoromethyl)phenyl)methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1190763-78-0

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1190763-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1190763-78-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,0,7,6 and 3 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1190763-78:
(9*1)+(8*1)+(7*9)+(6*0)+(5*7)+(4*6)+(3*3)+(2*7)+(1*8)=170
170 % 10 = 0
So 1190763-78-0 is a valid CAS Registry Number.

1190763-78-0Downstream Products

1190763-78-0Relevant academic research and scientific papers

Optimization of novel oxidative DIMs as Nur77 modulators of the Nur77-Bcl-2 apoptotic pathway

Tu, Xuhuang,Chen, Xiaohui,Zhang, Dongliang,Gao, Meichun,Liang, Jingmei,Bao, Guoliang,Zhang, Jie,Peng, Shuangzhou,Zhang, Xiaokun,Zeng, Zhiping,Su, Ying

, (2020/12/07)

Nur77, an orphan nuclear receptor, is a member of the nuclear receptor superfamily. Nur77 plays important roles in various biological processes. Previously we reported that BI1071(DIM-C-pPhCF3+MeSO3-), an oxidiz

The direct asymmetric alkylation of α-amino aldehydes with 3-indolylmethanols by enamine catalysis

Guo, Zhi-Lei,Xue, Jia-Hui,Fu, Li-Na,Zhang, Shun-En,Guo, Qi-Xiang

supporting information, p. 6472 - 6475 (2015/01/16)

This work describes an efficient α-alkylation reaction of α-amino aldehydes with 3-indolylmethanols. In the promotion of catalyst 3f, the target products were obtained in high yields (up to 99%), good diastereoselectivities (up to 88:12), and excellent en

Highly enantioselective alkylation reaction of enamides by bronsted-acid catalysis

Guo, Qi-Xiang,Peng, Yun-Gul,Zhang, Jin-Wei,Song, Liu,Feng, Zhang,Gong, Liu-Zhu

supporting information; experimental part, p. 4620 - 4623 (2009/12/09)

The H8-BINOL-derived, phosphoric acid catalyzed, highly enatioselective alkylation reaction of enamides with Indoiyl alcohols has been described. A phosphoric acid derived from H8-BINOL enabled an asymmetric α-alkylation of enamides with indoiy

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