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88190-77-6

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88190-77-6 Usage

General Description

6-CHLORO-4-PHENYL-3, 4-DIHYDROQUINAZOLINE-2-CARBOXYLIC ACID is a chemical compound with the molecular formula C16H12ClNO2. It is a quinazoline derivative with a chloro and phenyl group attached to the 6 and 4 position, respectively. It also contains a carboxylic acid group at the 2 position. 6-CHLORO-4-PHENYL-3, 4-DIHYDROQUINAZOLINE-2-CARBOXYLIC ACID is often used in medicinal and pharmaceutical research as it exhibits potential biological activities and can be used as a building block in the synthesis of other organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 88190-77-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,9 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88190-77:
(7*8)+(6*8)+(5*1)+(4*9)+(3*0)+(2*7)+(1*7)=166
166 % 10 = 6
So 88190-77-6 is a valid CAS Registry Number.

88190-77-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-4-phenyl-1,4-dihydroquinazoline-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 6-chloro-3,4-dihydro-4-phenylquinazoline-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:88190-77-6 SDS

88190-77-6Relevant articles and documents

Reactions of hydroxyglycines. New synthetic routes to 4-phenylquinazoline derivatives

Hoefnagel,Van Koningsveld,Van Meurs,Peters,Sinnema,Van Bekkum

, p. 6899 - 6912 (2007/10/02)

Reaction of hydroxyglycine with 2-aminobenzophenones gives 1,2-dihydro-4-phenyl-quinazoline-2-carboxylic acids in high yields and under mild conditions. These can be smoothly converted into the corresponding 3,4-dihydro isomers and into quinazoline derivatives via rearrangement and oxidation by air, respectively. The X-ray crystallographic structure of 6-chloro-1,2-dihydro-1-methyl-4-phenylquinazoline-2-carboxylic acid shows the carboxylate group at C(2) and the methyl group at N(1) to be in axial positions.

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