14370-74-2 Usage
General Description
3-Hydroxy-1H-indole-2-carboxylic acid ethyl ester is a chemical compound with a molecular formula of C11H11NO3. It is an ethyl ester of 3-hydroxyindole-2-carboxylic acid, which is a derivative of indole and an intermediate in the synthesis of various pharmaceutical compounds. 3-HYDROXY-1H-INDOLE-2-CARBOXYLIC ACID ETHYL ESTER has been studied for its potential applications in the pharmaceutical industry, particularly in the development of new drugs and therapeutics. It exhibits biological activity and has been investigated for its antimicrobial, antiviral, and anti-inflammatory properties. Additionally, 3-Hydroxy-1H-indole-2-carboxylic acid ethyl ester has been identified as a potential lead compound for further medicinal chemistry studies.
Check Digit Verification of cas no
The CAS Registry Mumber 14370-74-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,7 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14370-74:
(7*1)+(6*4)+(5*3)+(4*7)+(3*0)+(2*7)+(1*4)=92
92 % 10 = 2
So 14370-74-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO3/c1-2-15-11(14)9-10(13)7-5-3-4-6-8(7)12-9/h3-6,12-13H,2H2,1H3
14370-74-2Relevant articles and documents
ARYL AND HETEROARYL-CARBOXAMIDE SUBSTITUTED HETEROARYL COMPOUNDS AS TYK2 INHIBITORS
-
, (2021/10/15)
Novel carboxamide substituted compounds of Formula (I) are disclosed; as well as processes for their preparation, pharmaceutical compositions comprising them and their use in therapy as inhibitors of Tyrosine Kinase 2 (Tyk2).
3-substituted indole antiproliferative angiogenesis inhibitors
-
, (2008/06/13)
3-Substituted indole carbohydrazides having the formula are useful for inhibiting angiogenesis and cell proliferation. Also disclosed are compositions which inhibit angiogenesis and cell proliferation and methods of inhibiting angiogenesis and cancer in a mammal.
Regiospecific functionalization of indole-2-carboxylates and diastereoselective preparation of the corresponding indolines
Collot, Valerie,Schmitt, Martine,Marwah, Padma,Bourguignon, Jean-Jacques
, p. 2823 - 2847 (2007/10/03)
The N-acyl derivatives of 3-substituted indole-2-carboxylates prepared through several routes were submitted to catalytic hydrogenation affording either cis- or trans-indoline diastereomers after quantitative C-2 epimerization.
