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Pyridine, 2,6-bis(methylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58819-71-9

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58819-71-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58819-71-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,8,1 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 58819-71:
(7*5)+(6*8)+(5*8)+(4*1)+(3*9)+(2*7)+(1*1)=169
169 % 10 = 9
So 58819-71-9 is a valid CAS Registry Number.

58819-71-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-bis(methylsulfanyl)pyridine

1.2 Other means of identification

Product number -
Other names Pyridine,2,6-bis(methylthio)

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:58819-71-9 SDS

58819-71-9Downstream Products

58819-71-9Relevant academic research and scientific papers

One-pot double functionalisation of π-deficient heterocyclic lithium reagents

Chartoire, Anthony,Comoy, Corinne,Fort, Yves

, p. 1839 - 1845 (2011)

Herein, we report an efficient method for the double functionalisation of lithiated halogenopyridines, -pyrazines or -furopyridines through a convenient one-pot electrophilic trapping/nucleophilic substitution sequence.

POLYORGANOMETALLIC HETEROCYCLES. 2,6-DILITHIOPYRIDINE

Newkome, George R.,Roper, Jerry M.

, p. 147 - 153 (2007/10/02)

Metal-halogen exchange between 2,6-diiodo- and 2,6-dibromopyridine and two equivalents of n-butyllithium gives 2,6-dilithiopyridine.On quenching with either carbon dioxide followed by esterification, methanol or dimethyl disulfide the dilithio compound gives a methyl 2,6-pyridinedicarboxylate, pyridine, or 2,6-dithiomethylpyridine, respectively.A convenient procedure for halogen-halogen exchange is also described.

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