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2-phenyl-5-(trifluoromethoxy)-1H-indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

906774-22-9

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906774-22-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 906774-22-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,6,7,7 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 906774-22:
(8*9)+(7*0)+(6*6)+(5*7)+(4*7)+(3*4)+(2*2)+(1*2)=189
189 % 10 = 9
So 906774-22-9 is a valid CAS Registry Number.

906774-22-9Downstream Products

906774-22-9Relevant academic research and scientific papers

Chiral Br?nsted Acid from Chiral Phosphoric Acid Boron Complex and Water: Asymmetric Reduction of Indoles

Yang, Kai,Lou, Yixian,Wang, Chenglan,Qi, Liang-Wen,Fang, Tongchang,Zhang, Feng,Xu, Hetao,Zhou, Lu,Li, Wangyang,Zhang, Guan,Yu, Peiyuan,Song, Qiuling

, p. 3294 - 3299 (2020/01/21)

A new chiral Br?nsted acid, generated in situ from a chiral phosphoric acid boron (CPAB) complex and water, was successfully applied to asymmetric indole reduction. This “designer acid catalyst”, which is more acidic than TsOH as suggested by DFT calculations, allows the unprecedented direct asymmetric reduction of C2-aryl-substituted N-unprotected indoles and features good to excellent enantioselectivities with broad functional group tolerance. DFT calculations and mechanistic experiments indicates that this reaction undergoes C3-protonation and hydride-transfer processes. Besides, bulky C2-alkyl-substituted N-unprotected indoles are also suitable for this system.

INDOLE DERIVATIVE OR PHARMACEUTICALLY ACCEPTABLE SALT THEREOF

-

, (2012/06/01)

A compound (I) of the present invention, which has an EP1 receptor antagonism: [wherein A represents a benzene ring or the like; Y1 represents a C1-6 alkylene group; Y2 represents a single bond or the like; Rsu

Intramolecular Ir(I)-catalyzed benzylic C-H bond amination of ortho-substituted aryl azides

Sun, Ke,Sachwani, Rachna,Richert, Kathleen J.,Driver, Tom G.

supporting information; experimental part, p. 3598 - 3601 (2011/02/23)

Image Persented Iridium(I) catalyzes the intramolecular benzylic C-H bond amination of ortho-homobenzyl-substituted aryl azides to produce indolines at 25 °C.

Dirhodium(II)-catalyzed intramolecular C-H amination of aryl azides

Shen, Meihua,Leslie, Brooke E.,Driver, Tom G.

supporting information; experimental part, p. 5056 - 5059 (2009/03/11)

(Chemical Equation Presented) Azides to indoles: Dirhodium(II)-catalyzed decomposition of aryl azides was developed as a mild, functional group tolerant method for the synthesis of indoles (see scheme).

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