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4-[(1H-indol-3-yl)methyl]-N,N-diethylbenzenamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

134627-71-7

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134627-71-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134627-71-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,6,2 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 134627-71:
(8*1)+(7*3)+(6*4)+(5*6)+(4*2)+(3*7)+(2*7)+(1*1)=127
127 % 10 = 7
So 134627-71-7 is a valid CAS Registry Number.

134627-71-7Downstream Products

134627-71-7Relevant academic research and scientific papers

ZnCl2 promoted efficient, one-pot synthesis of 3-arylmethyl and diarylmethyl indoles

Subramaniapillai, Selva Ganesan,Ganesan, Asaithampi

, p. 694 - 698 (2014)

Anhydrous ZnCl2 mediated convenient, one-pot synthesis of 3-arylmethyl and diarylmethyl indoles was accomplished in good yields. Under reaction condition, in situ formation of kinetically stable bis(indolyl)methane product was identified. Its s

Ruthenium-catalyzed alkylation of indoles with tertiary amines by oxidation of a sp3 CH bond and lewis acid catalysis

Wang, Ming-Zhong,Zhou, Cong-Ying,Wong, Man-Kin,Che, Chi-Ming

experimental part, p. 5723 - 5735 (2010/08/20)

Ruthenium porphyrins (particularly [Ru(2,6-Cl2tpp)CO]; tpp = tetraphenylporphinato) and RuCl3 can act as oxidation and/or Lewis acid catalysts for direct C-3 alkylation of indoles, giving the desired products in high yields (up to 82

A novel multi-component reaction of indole, formaldehyde, and tertiary aromatic amines

Kumar, Atul,Sharma, Siddharth,Maurya, Ram Awatar

experimental part, p. 5937 - 5940 (2010/01/18)

A novel multi-component reaction of indoles, formaldehydes, and tertiary aromatic amines is described for the synthesis of dialkylaminoarylated indoles using silica-supported perchloric acid (HClO4-SiO2) as an inexpensive and highly efficient catalyst. The key features of this multi-component reactions are operational simplicity, mild reaction conditions, regioselectivity, and recycling of catalyst.

Benzotriazole as a Synthetic Auxiliary: Advantageous Syntheses of Substituted Diarylmethanes and Heterocyclic Analogues

Katritzky, Alan R.,Lan, Xiangfu,Lam, Jamshed N.

, p. 4397 - 4403 (2007/10/02)

4-(Benzotriazol-1-ylmethyl)-N,N-dimethylaniline (1b) can be substituted at the CH2 link via lithiation.Both the parent and substituted derivatives react with a variety of electron-rich benzenoid and heteroaromatic compounds in a novel approach to leuco dy

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