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37472-94-9

37472-94-9

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  • 6-Amino-1,2,3,4-tetrahydro-1,3-dimethyl-2,4-dioxo-5-pyrimidinecarboxylic acid ethyl ester

    Cas No: 37472-94-9

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  • 6-Amino-1,2,3,4-tetrahydro-1,3-dimethyl-2,4-dioxo-5-pyrimidinecarboxylic acid ethyl ester

    Cas No: 37472-94-9

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37472-94-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37472-94-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,4,7 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 37472-94:
(7*3)+(6*7)+(5*4)+(4*7)+(3*2)+(2*9)+(1*4)=139
139 % 10 = 9
So 37472-94-9 is a valid CAS Registry Number.

37472-94-9SDS

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 ethyl 4-amino-1,3-dimethyl-2,6-dioxopyrimidine-5-carboxylate

1.2 Other means of identification

Product number -
Other names 6-amino-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid ethyl ester

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:37472-94-9 SDS

37472-94-9Relevant articles and documents

Tandem reactions using nitrile imines: Synthesis of some novel heterocyclic compounds with expected biological activity

Gobouri, Adil A. H.,Mohamed, Mosselhi A. N. M.,Amin, Mahmoud A.

, p. 149 - 158 (2016)

New functionalized 7,9-dimethylpyrimido[4,5-d][1,2,4]triazolo[4,3-a]pyrimidine-5,6,8(1H,7H,9H)-trione derivatives were synthesized via reaction of the hydrazonoyl halides with 7,8-dihydro-1,3-dimethyl-7-thioxopyrimido[4,5-d]pyrimidine-2,4,5(1H,3H,6H)trione. The biological activity of the products has been evaluated. The mechanism and the regioselectivity of the studied reactions have been discussed.

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