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84658-14-0

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84658-14-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84658-14-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,6,5 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 84658-14:
(7*8)+(6*4)+(5*6)+(4*5)+(3*8)+(2*1)+(1*4)=160
160 % 10 = 0
So 84658-14-0 is a valid CAS Registry Number.

84658-14-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methoxy-4,6-bismethylthio-1,3,5-triazine

1.2 Other means of identification

Product number -
Other names -

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:84658-14-0 SDS

84658-14-0Relevant articles and documents

Regioselective Reactions in Heteroaromatic Systems. Rules for Methyl Migration and Nucleophilic Substitution in Methyl Cyanurates and Thiocyanurates

Tosato, Maria Livia,Soccorsi, Laura

, p. 1321 - 1326 (2007/10/02)

A comparative analysis carried out on 19 methyl cyanurates and thiocyanurates (some of which reported for the first time) allowed the following general conclusions to be drawn about their reactivity in nucleophilic substitution and thermal isomerisation reactions.The nucleophilic substitution of the methylthio-groups by methoxide anions is always possible, but requires different experimental conditions which are specific for the molecular region in which the methylthio is located; the thermal isomerisation reaction of the methoxy-derivatives into the corresponding S- or N-methyl isomers requires temperature conditions which are also largely dependent upon the molecular site of the methoxy-group.In both reactions the reactivity is enhanced by local asymmetry of substitution at the ring carbon atom to which the XMe (X=S or O) group is bound.

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