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4-methyl-6-methylsulfanyl-pyrimidin-2-amine is an organic compound with the molecular formula C6H9N3S. It is a derivative of pyrimidin-2-amine, featuring a methyl group at the 4th position and a methylsulfanyl (methylthio) group at the 6th position. 4-methyl-6-methylsulfanyl-pyrimidin-2-amine is characterized by its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its role as an intermediate in the production of certain chemical compounds. Its chemical structure and properties make it a valuable building block in the development of new molecules with specific therapeutic or pesticidal activities.

6307-46-6

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6307-46-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6307-46-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6307-46:
(6*6)+(5*3)+(4*0)+(3*7)+(2*4)+(1*6)=86
86 % 10 = 6
So 6307-46-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H9N3S/c1-4-3-5(10-2)9-6(7)8-4/h3H,1-2H3,(H2,7,8,9)

6307-46-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-6-methylsulfanylpyrimidin-2-amine

1.2 Other means of identification

Product number -
Other names 4-methyl-6-methylsulfanyl-pyrimidin-2-ylamine

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 -
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More Details:6307-46-6 SDS

6307-46-6Downstream Products

6307-46-6Relevant academic research and scientific papers

Heterocyclization of acetylketene N,S-acetals with benzoyl cyanamide

Dorokhov,Komkov,Bogdanov

, p. 1969 - 1970 (1997)

N-Unsubstituted mono- and diacetylketene N,S-acetals undergo cyclization with benzoyl cyanamide to form 2-amino-4-methylthiopyrimidine derivatives.

Synthesis and Plant Growth Stimulating Action of 2-Amino-6-methylpyrimidine-4(3H)-thione Derivatives

Hambardzumyan, E. N.,Shahbazyan, L. V.,Vorskanyan, A. S.,Yengoyan, A. P.

, p. 208 - 216 (2020/04/17)

Abstract: A series of new pyrimidine derivatives, including those containing an azole or azine heterocycle linked through a sulfur atom or a thiomethylene group, was synthesized based on 2-amino-6-methylpyrimidine-4(3H)-thione. The synthesized compounds exhibited a pronounced stimulating effect on plants growth in the range of 43–96% compared to heteroauxin.

Dimerizing condensation of alkylidenepropanedinitriles and alkylidenecyanamides. - A general approach to aniline, aminopyridine, and aminopyridine derivatives

Hartke,Sauerbier,Richter

, p. 279 - 284 (2007/10/02)

The base catalyzed dimerizing condensation of (α-methylthioalkylidene)propanedinitriles (e.g. 8) yields 2-aminobenzene-1,3-dicarbonitriles (e.g. 13), of (α-methylthioalkylidene)cyanamides (e.g. 14) 2-aminopyrimidines (e.g. 16, 37). The mixed condensation

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