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4-METHYL-6-(METHYLTHIO)-1,3,5-TRIAZIN-2-AMINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27622-90-8

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27622-90-8 Usage

Synthesis Reference(s)

Journal of Heterocyclic Chemistry, 27, p. 1565, 1990 DOI: 10.1002/jhet.5570270608

Check Digit Verification of cas no

The CAS Registry Mumber 27622-90-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,6,2 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27622-90:
(7*2)+(6*7)+(5*6)+(4*2)+(3*2)+(2*9)+(1*0)=118
118 % 10 = 8
So 27622-90-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H8N4S/c1-3-7-4(6)9-5(8-3)10-2/h1-2H3,(H2,6,7,8,9)

27622-90-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Methyl-6-(methylthio)-1,3,5-triazin-2-amine

1.2 Other means of identification

Product number -
Other names 4-methyl-6-methylsulfanyl-1,3,5-triazin-2-amine

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:27622-90-8 SDS

27622-90-8Downstream Products

27622-90-8Relevant academic research and scientific papers

Process for the preparation of 2-amino-s-triazines

-

, (2008/06/13)

The present invention relates to a process for the preparation of 2-amino-s-triazines in three stages. In the first stage nitriles, alcohols and hydrogen chloride are reacted to form the corresponding imido-ester hydrochlorides. In the second stage, the imido-ester hydrochlorides are reacted with cyanamide in the aqueous phase to form the N-cyanimido-esters, which comprises carrying out the first stage in the presence of acetic acid esters and the second stage in an aqueous solution which has been brought to a pH value of 5-8 by addition of bases, and reacting the N-cyanimido-esters with O-alkylisourea, S-alkylisothiourea, guanidine or amidine salts in the presence of a base in the third stage. The 2-amino-s-triazines can be prepared in a high purity and with good yields in this manner.

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