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1-[4-(dimethylamino)phenyl]-2-quinazolin-4(3H)-ylideneethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85957-41-1

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85957-41-1 Usage

Type of compound

Quinazolinone derivative

Substituents

a. Substituted phenyl group
b. Dimethylamino group

Physical appearance

Yellow to orange powder

Potential properties

Pharmaceutical properties

Possible applications

a. Medicine
b. Drug development for various diseases and conditions

Further evaluation

Requires research and testing to determine exact uses and properties

Check Digit Verification of cas no

The CAS Registry Mumber 85957-41-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,9,5 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 85957-41:
(7*8)+(6*5)+(5*9)+(4*5)+(3*7)+(2*4)+(1*1)=181
181 % 10 = 1
So 85957-41-1 is a valid CAS Registry Number.

85957-41-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2Z)-1-[4-(dimethylamino)phenyl]-2-(3H-quinazolin-4-ylidene)ethanone

1.2 Other means of identification

Product number -
Other names -

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:85957-41-1 SDS

85957-41-1Downstream Products

85957-41-1Relevant academic research and scientific papers

SYNTHESES OF 1-PHENYL-2-(4(1H)-QUINAZOLINYLIDENE)ETHANONE AND RELATED ETHANONES.

Sund,Beall,Borgfeld

, p. 428 - 429 (2007/10/02)

Eleven 1-phenyl-2-(4(1H)-quinazolinylidene)ethanones were synthesized by the condensation of 4-methylquinazoline and the requiste methyl benzoate ester with sodium hydride as the condensing agent. Substitutents in the 3- or 4-positions of the phenyl ring were chloro, dimethylamino, methoxy, methyl, and trifluoromethyl.

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