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N(1),N(3)-diallyl-6-methyluracil is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62899-01-8

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62899-01-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62899-01-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,8,9 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62899-01:
(7*6)+(6*2)+(5*8)+(4*9)+(3*9)+(2*0)+(1*1)=158
158 % 10 = 8
So 62899-01-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N2O2/c1-4-6-12-9(3)8-10(14)13(7-5-2)11(12)15/h4-5,8H,1-2,6-7H2,3H3

62899-01-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methyl-1,3-bis(prop-2-enyl)pyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 2,4(1H,3H)-Pyrimidinedione,6-methyl-1,3-di-2-propenyl

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:62899-01-8 SDS

62899-01-8Relevant academic research and scientific papers

Alkylation of 6-methyluracil and its derivatives

Krivonogov,Tolstikov,Murinov,Spirikhin,Fatykhov,Abdrakhmanov

, p. 301 - 306 (2007/10/03)

Alkylation of 6-methyluracil, 5-hydroxy-6-methyluracil, and 6-methyluracil-5-ammonium sulfate by allyl and propynyl bromide in DMF in the presence of K2CO3 and tetrabutylammonium bromide and the reaction products were studied.

SYNTHESIS AND ANTIVIRAL ACTIVITY OF ACYCLIC NUCLEOSIDE ANALOGUES OF 6-METHYLURACIL AND 4-ALKYLAMINO-6-METHYL-2(1H)-PYRIMIDINONES

Bhat, Sunita

, p. 683 - 690 (2007/10/02)

Reaction of 2,4-dimethoxy-6-methylpyrimidine (I) with allyl bromide or benzyl bromide afforded 1-substituted 4-methoxy-6-methyl-2(1H)-pyrimidinone intermediates III, X.Oxidation of the compound III afforded racemic cis diol VI.O-Demethylation and nucleophilic displacement of the intermediates III, VI, and X gave 1-substituted 6-methyluracils IV, VII, IX and 1-substituted 4-alkylamino-6-methyl-2(1H)-pyrimidinones V, VIII, XII in good yields.The compounds II - XII were evaluated against Ranikhet desease virus (RDV); compounds Vb, Vii, X, XIIb - XIId showed 100, 43, 44, 75, 72 and 100percent inhibition, respectively.

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