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155883-52-6

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155883-52-6 Usage

General Description

1-Carbamoyl-2,3-dihydro-1H-indole-2-carboxylic acid is a chemical compound with the molecular formula C11H12N2O3. It is a derivative of indole-2-carboxylic acid with a carbamoyl group attached to the nitrogen atom. 1-CARBAMOYL-2,3-DIHYDRO-1H-INDOLE-2-CARBOXYLIC ACID is a potential intermediate in the synthesis of various pharmaceuticals and biologically active molecules. Its structure and properties make it suitable for use in the development of new drugs and as a key building block in organic synthesis. The chemical properties and potential biological activities of 1-Carbamoyl-2,3-dihydro-1H-indole-2-carboxylic acid make it an important target for research and development in the fields of medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 155883-52-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,8,8 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 155883-52:
(8*1)+(7*5)+(6*5)+(5*8)+(4*8)+(3*3)+(2*5)+(1*2)=166
166 % 10 = 6
So 155883-52-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2O3/c11-10(15)12-7-4-2-1-3-6(7)5-8(12)9(13)14/h1-4,8H,5H2,(H2,11,15)(H,13,14)

155883-52-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-carbamoyl-2,3-dihydroindole-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-CARBAMOYL-2,3-DIHYDRO-1H-INDOLE-2-CARBOXYLIC ACID

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:155883-52-6 SDS

155883-52-6Relevant articles and documents

Preparation and reaction of 3-oxo-3H-pyrazolo[1,5-a]indole derivatives

Shen,Katayama

, p. 222 - 227 (1994)

An alternative method to prepare 3-oxo-2-phenyl-3H-pyrazolo[1,5-a]indole starting from indoline-2-carboxylic acid was explored. The reaction with nucleophilic agents allowed us to introduce the properly substituted alkyl substituents at C-4 of the 4H-pyrazolo[1,5-a]indoles. The 2,3-dichloro-5,6- dicyano-p-benzoquinone (DDQ) oxidation of these products gave the 3-oxo-2- phenyl-3H-pyrazolo[1,5-a]indole derivatives. Selective keto-enol tautomerizations of these 1,5-diketo-monoene system were observed.

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