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36946-02-8

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36946-02-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36946-02-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,9,4 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 36946-02:
(7*3)+(6*6)+(5*9)+(4*4)+(3*6)+(2*0)+(1*2)=138
138 % 10 = 8
So 36946-02-8 is a valid CAS Registry Number.

36946-02-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-5-butyl-3-ethyl-6-methylpyrimidin-4-one

1.2 Other means of identification

Product number -
Other names 4(3H)-Pyrimidinone,2-amino-5-butyl-3-ethyl-6-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:36946-02-8 SDS

36946-02-8Relevant articles and documents

NEW AMINOPYRIMIDINONIC DERIVATIVES WITH POTENTIAL BIOLOGICAL ACTIVITY

Mager, Sorin,Cristea, I.,Craciun, Liliana,Irimie, F.,Diudea, M.

, p. 665 - 670 (2007/10/03)

In the industrial synthesis of fungicide, ethyrimol (I) (5-butyl-2-ethylamino-6-methyl-4-pyrimidinol), starting from ethylguanidine nitrate and butylacetoacetic ester, a by product (15 percent of the main product) was also formed: the 2-amino-5-butyl-3-ethyl-4-pyrimidinone (II). In order to render valuable this by-product by means of some of its potentially biologic active derivatives, its 2-amino function was used. By acylation with phenoxyacetyl chlorides, tosyl chloride, p-acetylaminobenzenesulfonic chloride, the corresponding amides were obtained. The amino function was also replaced by the hydroxyl and chlorine groups. With phosgene the N,N-disubstituted urea was obtained. The new compounds were characterized by means of 1H-NMR and IR spectra, some of them proving a biological activity.

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