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132973-51-4

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132973-51-4 Usage

General Description

DiMethyl 2-(Methylthio)pyriMidine-4,5-dicarboxylate is a chemical compound with a complex molecular structure containing two methyl groups, a methylthio group, and a pyrimidine ring. It is an ester derivative of pyrimidine-4,5-dicarboxylic acid, a type of organic compound. This chemical may be used in research or industrial processes as a building block for the synthesis of various other compounds. Its specific properties and potential uses would depend on the context of its application and the specific reactions in which it is involved.

Check Digit Verification of cas no

The CAS Registry Mumber 132973-51-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,9,7 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 132973-51:
(8*1)+(7*3)+(6*2)+(5*9)+(4*7)+(3*3)+(2*5)+(1*1)=134
134 % 10 = 4
So 132973-51-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H10N2O4S/c1-14-7(12)5-4-10-9(16-3)11-6(5)8(13)15-2/h4H,1-3H3

132973-51-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2-methylsulfanylpyrimidine-4,5-dicarboxylate

1.2 Other means of identification

Product number -
Other names 4,5-dimethoxycarbonyl-2-methylsulfanylpyrimidine

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:132973-51-4 SDS

132973-51-4Downstream Products

132973-51-4Relevant articles and documents

Cationic 1,3-diazadienes in annulation reactions. Synthesis of pyrimidine, thiadiazinedioxide and triazine derivatives

Landreau,Deniaud,Reliquet,Reliquet,Meslin

, p. 93 - 98 (2007/10/03)

Triazapentadienium iodides 2 prepared from N'-thiocarbamoylformamidines 1 are efficient intermediates in heterocyclic synthesis. They react with ketenes, sulfenes, phenyl isocyanate or isothiocyanate and dimethyl acetylenedicarboxylate affording the corre

SYNTHESIS AND DIELS-ALDER REACTION OF STABLE ARYL FREE 1,3-DIAZABUTADIENE

Ibnusaud, Ibrahim,Padma Malar, E. J.,Sundaram, Narayanaswamy

, p. 7357 - 7358 (2007/10/02)

The Diels-Alder reactions of 1-methoxycarbonyl-4-dimethylamino-2-thiomethyl-1,3-diazabutadiene with dimethyl acetylenedicarboxylate (DMAD) and monophenyl ketene give pyrimidines in one pot.

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