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84212-03-3

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84212-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84212-03-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,2,1 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 84212-03:
(7*8)+(6*4)+(5*2)+(4*1)+(3*2)+(2*0)+(1*3)=103
103 % 10 = 3
So 84212-03-3 is a valid CAS Registry Number.

84212-03-3SDS

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 N-methyl-1-(4-methylsulfanylphenyl)methanamine

1.2 Other means of identification

Product number -
Other names N-methyl-4-methylthiobenzylamine

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:84212-03-3 SDS

84212-03-3Relevant articles and documents

Selective synthesis of mono- and di-methylated amines using methanol and sodium azide as C1 and N1 sources

Chakrabarti, Kaushik,Mishra, Anju,Panja, Dibyajyoti,Paul, Bhaskar,Kundu, Sabuj

supporting information, p. 3339 - 3345 (2018/07/29)

A Ru(ii) complex mediated synthesis of various N,N-dimethyl and N-monomethyl amines from organic azides using methanol as a methylating agent is reported. This methodology was successfully applied for a one-pot reaction of bromide derivatives and sodium azide in methanol. Notably, by controlling the reaction time several N-monomethylated and N,N-dimethylated amines were synthesized selectively. The practical applicability of this tandem process was revealed by preparative scale reactions with different organic azides and synthesis of an anti-vertigo drug betahistine. Several kinetic experiments and DFT studies were carried out to understand the mechanism of this transformation.

Cyclisation of Benzylaminonitriles. Part 5. Alkylthio and Arylthio Activating Groups.

Euerby, Melvin R.,Waigh, Roger D.

, p. 2417 - 2460 (2007/10/02)

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