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2-[(2-Chlorobenzyl)thio]-3-phenylquinazolin-4(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74333-00-9

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74333-00-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74333-00-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,3,3 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 74333-00:
(7*7)+(6*4)+(5*3)+(4*3)+(3*3)+(2*0)+(1*0)=109
109 % 10 = 9
So 74333-00-9 is a valid CAS Registry Number.
InChI:InChI=1/C21H15ClN2OS/c22-18-12-6-4-8-15(18)14-26-21-23-19-13-7-5-11-17(19)20(25)24(21)16-9-2-1-3-10-16/h1-13H,14H2

74333-00-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2-chlorophenyl)methylsulfanyl]-3-phenylquinazolin-4-one

1.2 Other means of identification

Product number -
Other names 2-(o-Chlorobenzylthio)-3-phenyl-4(3H)quinazolinone

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:74333-00-9 SDS

74333-00-9Downstream Products

74333-00-9Relevant academic research and scientific papers

Synthesis of thioether derivatives of quinazoline-4-one-2-thione and evaluation of their antiplatelet aggregation activity

Eskandariyan, Zahra,Esfahani Zadeh, Marjan,Haj Mohammad Ebrahim Tehrani, Kamaleddin,Mashayekhi, Vida,Kobarfard, Farzad

, p. 332 - 339 (2014/04/03)

A series of 2-(arylmethylthio)-3-phenylquinazolin-4-one derivatives have been synthesized and their antiplatelet aggregation activities were assessed against ADP and arachidonic acid-induced platelet aggregation in human plasma. Among the tested thioethers, derivative 2, 3, 5 and 16 were the most potent compounds with satisfactory IC50 for inhibition of platelet aggregation induced by ADP. Analysis of global physicochemical parameters shows some correlations between activities and molecular volume and also surface area of the studied derivatives.

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