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14370-74-2

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14370-74-2 Usage

Description

3-Hydroxy-1H-indole-2-carboxylic acid ethyl ester, with the molecular formula C11H11NO3, is an ethyl ester of 3-hydroxyindole-2-carboxylic acid. It is a derivative of indole and serves as an intermediate in the synthesis of various pharmaceutical compounds. This chemical compound 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. Furthermore, 3-Hydroxy-1H-indole-2-carboxylic acid ethyl ester has been identified as a potential lead compound for further medicinal chemistry studies.

Uses

Used in Pharmaceutical Industry:
3-Hydroxy-1H-indole-2-carboxylic acid ethyl ester is used as an intermediate in the synthesis of various pharmaceutical compounds for its potential applications in drug development.
Used in Antimicrobial Applications:
In the field of antimicrobial research, 3-Hydroxy-1H-indole-2-carboxylic acid ethyl ester is used as an antimicrobial agent, exhibiting properties that can help combat various types of bacteria.
Used in Antiviral Applications:
3-Hydroxy-1H-indole-2-carboxylic acid ethyl ester is utilized as an antiviral agent, showing potential in inhibiting the replication and spread of viruses.
Used in Anti-inflammatory Applications:
In the area of anti-inflammatory research, 3-Hydroxy-1H-indole-2-carboxylic acid ethyl ester is employed as an agent to reduce inflammation, potentially providing relief for various inflammatory conditions.
Used in Medicinal Chemistry Studies:
3-Hydroxy-1H-indole-2-carboxylic acid ethyl ester is used as a lead compound in medicinal chemistry studies, where it is further investigated and modified to enhance its therapeutic potential and optimize its properties for specific medical applications.

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

14370-74-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-hydroxy-1H-indole-2-carboxylate

1.2 Other means of identification

Product number -
Other names 3-hydroxy-indole-2-carboxylic acid ethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:14370-74-2 SDS

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.

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