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136819-96-0

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136819-96-0 Usage

Structure

A pyrimidine ring with a prop-2-en-1-yloxy group attached to the methyl carbon

Type of compound

Heterocyclic compound

Derivative of

Pyrimidine-2,4(1H,3H)-dione

Functional groups

Prop-2-en-1-yloxy, carbonyl, and amide groups

Applications

Organic synthesis, medicinal chemistry, and pharmaceutical drug development

Potential uses

Treatment of certain diseases or as a building block for the synthesis of other organic molecules

Check Digit Verification of cas no

The CAS Registry Mumber 136819-96-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,8,1 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 136819-96:
(8*1)+(7*3)+(6*6)+(5*8)+(4*1)+(3*9)+(2*9)+(1*6)=160
160 % 10 = 0
So 136819-96-0 is a valid CAS Registry Number.

136819-96-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(prop-2-enoxymethyl)pyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 2,4(1H,3H)-Pyrimidinedione,1-((2-propenyloxy)methyl)

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:136819-96-0 SDS

136819-96-0Downstream Products

136819-96-0Relevant articles and documents

Efficient synthesis of 3-hydroxymethylated cis- and trans-cyclobutane β-amino acids using an intramolecular photocycloaddition strategy

Mondière, Aurélie,Peng, Runhui,Remuson, Roland,Aitken, David J.

, p. 1088 - 1093 (2008/09/17)

Uracil bearing a tethered allyl alcohol appendage at N1 undergoes a [2+2] photocycloaddition reaction to provide a single tricyclic adduct in high yield. This compound is transformed in one step into a cis-cyclobutane β-amino acid bearing a 3-hydroxymethyl group. Through appropriate functionalization and epimerization, the trans isomer is obtained therefrom in only three further steps.

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