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918164-36-0

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918164-36-0 Usage

Chemical Class

Pyrimidinones

Physical Form

White to off-white solid

Synthesis

Used in the synthesis of pharmaceuticals

Organic Synthesis

Used as an intermediate in organic synthesis

Biological Activities

Studied for potential anti-inflammatory and anti-cancer properties

Industrial Applications

Versatile chemical with a range of applications in the pharmaceutical and chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 918164-36-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,1,6 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 918164-36:
(8*9)+(7*1)+(6*8)+(5*1)+(4*6)+(3*4)+(2*3)+(1*6)=180
180 % 10 = 0
So 918164-36-0 is a valid CAS Registry Number.

918164-36-0SDS

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-[2-(4-chlorophenyl)-2-oxoethyl]pyrimidin-2-one

1.2 Other means of identification

Product number -
Other names 2(1H)-Pyrimidinone,1-[2-(4-chlorophenyl)-2-oxoethyl]

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:918164-36-0 SDS

918164-36-0Relevant articles and documents

Novel and efficient synthesis of 2-aminooxazoles from pyrimidin-2(1H)-one

Alifanov, Vadim L.,Babaev, Eugene V.

, p. 263 - 270 (2007)

Stepwise conversion of pyrimidin-2(1H)-one to 2-amino-5-aryloxazoles via oxazolo[3,2-a]pyrimidinium salts is reported. The sequence involves, (i) regioselective N-alkylation of pyrimidone by phenacyl bromides, (ii) cyclization of obtained 1-(2-aryl-2-oxoethyl)pyrimidin-2(1H)-ones into oxazolo[3,2-a] pyrimidinium salts under the action of fuming sulfuric (or triflic) acid, and (iii) reaction of the obtained salts with hydrazine leading to 2-amino-5-aryloxazoles. Georg Thieme Verlag Stuttgart.

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