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1-Benzyl-2-chloro-indole is an organic compound with the molecular formula C15H12ClN and a molecular weight of 243.71 g/mol. It is a derivative of indole, a heterocyclic aromatic organic compound, and features a benzyl group attached to the 1-position and a chlorine atom at the 2-position. 1-benzyl-2-chloro-indole is often used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its unique structure and reactivity. It is typically synthesized through various chemical reactions, such as the Friedel-Crafts alkylation of indole with benzyl chloride, followed by chlorination. 1-Benzyl-2-chloro-indole is a white to off-white crystalline solid, soluble in organic solvents, and has a melting point of around 90-92°C. It is sensitive to light and moisture, and should be stored under cool, dry conditions to maintain its stability.

7135-34-4

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7135-34-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7135-34-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,3 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7135-34:
(6*7)+(5*1)+(4*3)+(3*5)+(2*3)+(1*4)=84
84 % 10 = 4
So 7135-34-4 is a valid CAS Registry Number.

7135-34-4Downstream Products

7135-34-4Relevant academic research and scientific papers

REACTION OF 3-INDOLYLPHENYLIODONIUM BETAINE WITH ELECTROPHILIC AGENTS

Budylin, V. A.,Ermolenko, M. S.,Chugtai, F. A.,Sharbatyan, P. A.,Kost, A. N.

, p. 1095 - 1097 (2007/10/02)

3-Indolylphenyliodonium chloride and bromide, respectively, were obtained by the action of hydrochloric and hydrobromic acids on 3-indolylphenyliodonium betaine.Pyrolysis of the chloride leads to a mixture of 2- and 3-chloroindoles,while pyrolysis the bromine leads only to 3-bromoindole. 1-Benzyl-2-chloroindole is obtained in the reaction of the betaine with benzyl chloride.The betaine reacts with dimethylsulfate to give an iodonium salt, the reaction of wich with lithium chloride and ammonium chloride leads to 1-methyl-2-chloroindole.

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