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87573-90-8

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87573-90-8 Usage

Chemical structure

A pyrimidinone derivative with a chlorine atom attached to a vinyl group

Usage

Can be used in various chemical reactions and syntheses

Potential applications

Pharmaceutical and agrochemical industries

Uses and applications

May vary based on specific properties and reactivity of the chemical

Toxicological and environmental impact

May impact the potential uses and applications of the chemical

Check Digit Verification of cas no

The CAS Registry Mumber 87573-90-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,7 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87573-90:
(7*8)+(6*7)+(5*5)+(4*7)+(3*3)+(2*9)+(1*0)=178
178 % 10 = 8
So 87573-90-8 is a valid CAS Registry Number.

87573-90-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(1-chlorolvinyl)-2-pyrimidinone

1.2 Other means of identification

Product number -
Other names 5-(1-Chloro-vinyl)-1H-pyrimidin-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:87573-90-8 SDS

87573-90-8Downstream Products

87573-90-8Relevant articles and documents

Syntheses and Reactions of Some 5-Vinyl- and 5-Ethynylpyrimidines

Benneche, Tore,Undheim, Kjell

, p. 235 - 240 (2007/10/02)

5-β,β-Dichlorovinyl- and 5-α-chlorovinylpyrimidines have been prepared from 5-acetyl-2-methylthiopyrimidines.HCl elimination from the 5-α-chlorovinyl derivatives yields the 5-ethynyl analogues.Peracid or chlorine oxidation of the sulfides yields the sulfones which may be hydrolyzed to the corresponding lactams.The reaction paths are discussed.

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