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 articles and documents
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.
