92622-96-3 Usage
Chemical class
Ester derivative
Explanation
It is a compound formed by the esterification of the carboxylic acid group of 3-bromo-5-methoxy-1H-indole-2-carboxylic acid with an alcohol (ethanol).
Explanation
It is commonly used in organic synthesis and pharmaceutical research as a starting material for the synthesis of various biologically active compounds.
Explanation
The compound has shown potential in the development of new drugs with these therapeutic properties, making it valuable in medicinal chemistry research.
Explanation
1H-INDOLE-2-CARBOXYLIC ACID, 3-BROMO-5-METHOXY-, ETHYL ESTER exhibits a range of pharmacological activities, which contributes to its importance in the development of new drugs and therapies.
Therapeutic applications
a. Anticancer
b. Anti-inflammatory
c. Antimicrobial
Check Digit Verification of cas no
The CAS Registry Mumber 92622-96-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,6,2 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 92622-96:
(7*9)+(6*2)+(5*6)+(4*2)+(3*2)+(2*9)+(1*6)=143
143 % 10 = 3
So 92622-96-3 is a valid CAS Registry Number.
92622-96-3Relevant academic research and scientific papers
Design, synthesis and biological evaluation of 2-alkoxycarbonyl-3-anilinoindoles as a new class of potent inhibitors of tubulin polymerization
Balzarini, Jan,Bortolozzi, Roberta,Brancale, Andrea,Ferla, Salvatore,Hamel, Ernest,Kimatrai Salvador, Maria,Liekens, Sandra,Oliva, Paola,Persoons, Leentje,Prencipe, Filippo,Romagnoli, Romeo,Schols, Dominique,Viola, Giampietro
, (2020/02/22)
A new class of inhibitors of tubulin polymerization based on the 2-alkoxycarbonyl-3-(3′,4′,5′-trimethoxyanilino)indole molecular skeleton was synthesized and evaluated for antiproliferative activity, inhibition of tubulin polymerization and cell cycle eff
REGIOSELECTIVE BROMINATION OF METHOXY DERIVATIVES OF ETHYL INDOLE-2-CARBOXYLATE
Tani, Masanobu,Ikegami, Hiroyo,Tashiro, Mayumi,Hiura, Tetsuji,Tsukioka, Hiroko,et al.
, p. 2349 - 2362 (2007/10/02)
Bromination of ethyl methoxyindole-2-carboxylate (1) with bromine in acetic acid proceeded on the benzene moiety of 1, whereas the reaction of 1 with pyridinium bromide perbromide in pyridine or N-bromosuccinimide in dimethylformamide gave ethyl 3-bromo-m
