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1-(CyclopropylMethyl)-4-phenylquinazolin-2(1H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33453-22-4

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33453-22-4 Usage

Family

Quinazolinone

Functional groups

Cyclopropylmethyl group
Phenyl substituent

Type

Organic compound

Potential applications

Pharmacological properties
Medicinal chemistry
Development of novel drug candidates

Further research needed

Specific biological activity
Potential uses
Investigation through research and testing

Check Digit Verification of cas no

The CAS Registry Mumber 33453-22-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,4,5 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 33453-22:
(7*3)+(6*3)+(5*4)+(4*5)+(3*3)+(2*2)+(1*2)=94
94 % 10 = 4
So 33453-22-4 is a valid CAS Registry Number.

33453-22-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(cyclopropylmethyl)-4-phenylquinazolin-2-one

1.2 Other means of identification

Product number -
Other names 1-cyclopropylmethyl-4-phenyl-1H-quinazolin-2-one

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:33453-22-4 SDS

33453-22-4Upstream product

33453-22-4Downstream Products

33453-22-4Relevant academic research and scientific papers

Process for preparing 2(1H)-quinazolinone derivatives

-

, (2008/06/13)

2(1H)-Quinazolinone and quinazolinethione derivatives having excellent pharmacological activities are produced in high yield with high purity by heating the corresponding 3,4-dihydro-2(1H)-quinazolinone or quinazolinethione derivatives together with sulfur in an inert solvent.

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