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1069123-92-7

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1069123-92-7 Usage

Structure

An ester of 1H-indole-3-carboxylic acid, 2,6-diMethyl

Type

Heterocyclic aromatic organic compound

Usage

Commonly used in the synthesis of pharmaceuticals and agrochemicals

Biological activities

Exhibits antimicrobial, anti-inflammatory, and anticancer properties

Importance

Important compound for the development of various therapeutic agents

Utilization

Used as a precursor for the synthesis of various drugs in the pharmaceutical industry, and as a key intermediate in the manufacturing of perfumes, flavorings, and other organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 1069123-92-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,9,1,2 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1069123-92:
(9*1)+(8*0)+(7*6)+(6*9)+(5*1)+(4*2)+(3*3)+(2*9)+(1*2)=147
147 % 10 = 7
So 1069123-92-7 is a valid CAS Registry Number.

1069123-92-7Downstream Products

1069123-92-7Relevant articles and documents

Copper(I)-catalyzed, one-pot synthesis of multisubstituted indoles from 2-iodoanilines and ethyl buta-2,3-dienoate

Wang, Xianxue,Liu, Jin,Guo, Han,Ma, Chao,Gao, Xiai,Zhou, Kang,Huang, Guosheng

, p. 1037 - 1042 (2012)

Reactions of 2-iodoanilines with ethyl buta-2,3-dienoate catalyzed by potassium carbonate and CuI in one pot generate the corresponding ethyl 2-methyl-1H-indole-3-carboxylate products in moderate yields under mild conditions. Georg Thieme Verlag Stuttgart · New York.

Copper-catalyzed synthesis of 2,3-disubstituted indoles from ortho-haloanilines and β-keto esters/β-diketone

Liu, Xiao-Guang,Li, Zi-Hao,Xie, Jian-Wei,Liu, Ping,Zhang, Jie,Dai, Bin

supporting information, p. 653 - 657 (2016/01/15)

Tetrazole-1-acetic acid was identified as an efficient ligand to promote copper-catalyzed domino reaction of ortho-iodo/bromo-anilines with β-keto esters/β-diketone for 2,3-disubstituted indoles' synthesis with high yields under mild conditions. The proto

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