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2(1H)-Pyrimidinone, 6-amino-5-(4-chlorobenzoyl)-1-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

353285-41-3

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353285-41-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 353285-41-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,3,2,8 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 353285-41:
(8*3)+(7*5)+(6*3)+(5*2)+(4*8)+(3*5)+(2*4)+(1*1)=143
143 % 10 = 3
So 353285-41-3 is a valid CAS Registry Number.

353285-41-3SDS

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 6-amino-5-(4-chlorobenzoyl)-1-methylpyrimidin-2-one

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:353285-41-3 SDS

353285-41-3Upstream product

353285-41-3Relevant academic research and scientific papers

A convenient route for the synthesis of 4-aryl- and 4-aminopyrimidines

Jachak, Madhukar N.,Tantak, Chanda D.,Toche, Raghunath B.,Badgujar, Naresh S.

, p. 1529 - 1538 (2007/10/03)

A series of ureidopropenenitriles were synthesised by Knoevenagel condensation of ArCOCH2CN and HC(OEt)3 in presence of ureas in a one potreaction. These ureidopropenenitriles were cyclised to 4-aryl-5-cyano-3-substituted pyrimidines (in acid) or to 4-amino-5- benzoylpyrimidines (in base) in 60-70% yields. The amine pyrimidine derivatives were further converted to substituted uracils by hydrolysis with isopentyl nitrite in DMF. Alkylation of uracils furnished 1,3-dimethyluracil derivatives with DMS in alkali. All new compounds were characterised by spectral and analytical methods. Springer-Verlag 2004.

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