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1H-Indole-1-carboxylic acid, 2-[(ethoxycarbonyl)oxy]-3-(phenylmethyl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

140701-17-3

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140701-17-3 Usage

Molecular structure

A chemical compound that is a derivative of indole-1-carboxylic acid, with an ethyl group attached to the carboxylic acid functional group and a phenylmethyl group attached to the indole ring.

Type of compound

An ester.

Functional groups

Carboxylic acid, ester, ethoxycarbonyl, phenylmethyl.

Uses

Commonly used in organic synthesis and pharmaceutical research as a building block or intermediate in the synthesis of various bioactive molecules.

Potential applications

May have potential applications in medicinal chemistry and drug development due to its structural features.

Check Digit Verification of cas no

The CAS Registry Mumber 140701-17-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,7,0 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 140701-17:
(8*1)+(7*4)+(6*0)+(5*7)+(4*0)+(3*1)+(2*1)+(1*7)=83
83 % 10 = 3
So 140701-17-3 is a valid CAS Registry Number.

140701-17-3Relevant academic research and scientific papers

Synthesis of 3-alkyl-3-bromo-1-ethoxycarbonyl-1,3-dihydro-2H-indol-2-ones

Beccalli,Marchesini

, p. 265 - 266 (1992)

3-Alkyl-1,3-dihydro-2H-indol-2-ones 1 are converted to the coresponding 2-ethoxycarbonyloxy derivatives 2 by reaction with ethyl chloroformate in the presence of triethylamine. Bromination of 2 affords the title compounds in 73-93% yield.

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