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1-(tert-butyldimethylsilyl)-N,N-diethyl-5-(4-methoxyphenyl)-1H-indole-4-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1415045-75-8

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1415045-75-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1415045-75-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,0,4 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1415045-75:
(9*1)+(8*4)+(7*1)+(6*5)+(5*0)+(4*4)+(3*5)+(2*7)+(1*5)=128
128 % 10 = 8
So 1415045-75-8 is a valid CAS Registry Number.

1415045-75-8Downstream Products

1415045-75-8Relevant academic research and scientific papers

Beyond directed ortho metalation: Ru-catalyzed CAr-O activation/cross-coupling reaction by amide chelation

Zhao, Yigang,Snieckus, Victor

, p. 11224 - 11227 (2014/09/29)

Disclosed is a new, catalytic, and general methodology for the chemical synthesis of biaryl, heterobiaryl, and polyaryl molecules by the cross-coupling of o-methoxybenzamides with aryl boroneopentylates. The reaction is based on the activation of the unreactive C-OMe bond by the proximate amide directing group using catalytic RuH2(CO)(PPh3)3 conditions. A one-step, base-free coupling process is thereby established that has the potential to supersede the useful two-step directed ortho metalation/cross- coupling reaction involving cryogenic temperature and strong base conditions. High regioselectivity, orthogonality with the Suzuki-Miyaura reaction, operational simplicity, minimum waste, and convenient scale-up make these reactions suitable for industrial applications.

Compounds and Methods for Catalytic Directed ortho Substitution of Aromatic Amides and Esters

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Page/Page column 22; 25; 51, (2012/12/13)

Methods are described for efficient and regioselective reactions that are Ru-catalyzed and either (i) amide-directed C—H, C—N, C—O activation/C—C bond forming reactions, (ii) ester-directed C—O and C—N activation/C—C bond forming reactions, or (iii) amide

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