137777-12-9 Usage
Derivative of indole
The compound is derived from the molecule indole, which is a heterocyclic aromatic compound that is a building block of many natural and synthetic compounds.
Cyclohexenyl moiety
The compound has a cyclohexenyl group (a six-carbon ring with one double bond) attached to the carboxylic acid group, which contributes to its chemical and biological properties.
Potential biological activities
1H-Indole-2-carboxylic acid, 1-(3-oxo-1-cyclohexen-1-yl)is being studied for its potential pharmacological properties, including its ability to affect biological processes.
Anti-inflammatory and anti-cancer effects
The compound is being studied for its potential to reduce inflammation and inhibit the growth of cancer cells.
Check Digit Verification of cas no
The CAS Registry Mumber 137777-12-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,7,7 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 137777-12:
(8*1)+(7*3)+(6*7)+(5*7)+(4*7)+(3*7)+(2*1)+(1*2)=159
159 % 10 = 9
So 137777-12-9 is a valid CAS Registry Number.
137777-12-9Relevant articles and documents
Rearrangements of Pyrrole and Indole Substituted Enol Esters of Cyclohexane-1,3-dione
Oliver, James E.,Lusby, William R.,Waters, Rolland M.
, p. 1565 - 1568 (2007/10/02)
Enol esters 3a and 3b, from cyclohexane-1,3-dione and pyrrole-2-carbonyl chloride and indole-2-carbonyl chloride, respectively, rearranged in the presence of triethylamine to the enamino acids 7 and 12.In the presence of cyanide, 3b, also underwent the expected rearrangement to 4b, whereas only 7 was formed from 3a.Treatment of 7 with mercuric acetate in hot acetic acid resulted in decarboxylation and aromatization to phenol 9.
