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3-(2-chlorobenzalamino)-2-ethyl-4(3H)-quinazolinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112447-53-7

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112447-53-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112447-53-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,4,4 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 112447-53:
(8*1)+(7*1)+(6*2)+(5*4)+(4*4)+(3*7)+(2*5)+(1*3)=97
97 % 10 = 7
So 112447-53-7 is a valid CAS Registry Number.

112447-53-7SDS

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 3-(2-chlorobenzalamino)-2-ethyl-4(3H)-quinazolinone

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:112447-53-7 SDS

112447-53-7Downstream Products

112447-53-7Relevant academic research and scientific papers

α-Arylazo-N-benzylidenimines Incorporating a Formazan Moiety

Singh, Shradha,Shukla, Mukundja,Srivastava, Vijai K.,Shanker, K.

, p. 368 - 370 (2007/10/02)

α-Arylazo-N-benzylidenimines (IIIa-o) have been prepared from 2-alkyl-3-substituted-benzalamino-4-quinazolin-4(3H)-ones (IIa-g) and diazonium salts.The quinazolinones in turn have been obtained by the reaction of 2-alkyl-

Antiparkinsonian Agents from Quinazolinylthiazolidinones and Azetidinones

Srivastava, Vijai K.,Singh, S.,Gulati, A.,Shanker, K.

, p. 652 - 656 (2007/10/02)

2-Alkyl-3-arylidenamino-4-quinazolinones (I) on reaction with thioglycolic acid and chloroacetyl chloride are changed into thiazolidinones (II) and azetidinones (III) respectively.Their structures have been delineated by mass spectroscopy.Some of the comp

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