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18368-57-5

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18368-57-5 Usage

General Description

2-Mercapto-6-methylpyridine 97 is a chemical compound with the molecular formula C6H7NS. It is a pyridine derivative that contains both a thiol group and a methyl group. 2-MERCAPTO-6-METHYLPYRIDINE 97 is commonly used in the synthesis of pharmaceuticals and agrochemicals, as well as in the production of rubber chemicals and corrosion inhibitors. It is also utilized as a building block in organic synthesis for various industrial applications. Additionally, 2-Mercapto-6-methylpyridine 97 is known for its strong odor and should be handled with care due to its potential irritant and harmful effects.

Check Digit Verification of cas no

The CAS Registry Mumber 18368-57-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,6 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18368-57:
(7*1)+(6*8)+(5*3)+(4*6)+(3*8)+(2*5)+(1*7)=135
135 % 10 = 5
So 18368-57-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H7NS/c1-5-3-2-4-6(8)7-5/h2-4H,1H3,(H,7,8)

18368-57-5 Well-known Company Product Price

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  • Aldrich

  • (642096)  2-Mercapto-6-methylpyridine  97%

  • 18368-57-5

  • 642096-1G

  • 1,289.34CNY

  • Detail
  • Aldrich

  • (642096)  2-Mercapto-6-methylpyridine  97%

  • 18368-57-5

  • 642096-5G

  • 4,264.65CNY

  • Detail

18368-57-5SDS

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 6-methyl-1H-pyridine-2-thione

1.2 Other means of identification

Product number -
Other names 6-Methyl-2-pyridinethiol

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:18368-57-5 SDS

18368-57-5Relevant articles and documents

Synthesis and characterization of 2-pyridylsulfur pentafluorides

Kanishchev, Oleksandr S.,Dolbier, William R.

, p. 280 - 284 (2015)

Current approaches to prepare SF5-substituted heterocycles during the synthesis of targeted heterocyclic compounds require the use of SF5-functionalized aryl or alkyne reagents or SF5Cl as a source of the SF5 functional group. Herein we report that excess oxidative fluorination of 2,2' -dipyridyl disulfide with a KF/Cl2 /MeCN system leads to the formation of thirteen new 2-pyridylsulfur chlorotetrafluorides (2-SF4Cl-pyridines). These molecules are found to undergo further chlorine-fluorine exchange reactions by treatment with silver(I) fluoride enabling ready access to a series of ten new substituted 2-pyridylsulfur pentafluorides (2-SF5-pyridines). This is the first preparatively simple and readily scalable example of the transformation of an existing heterocyclic sulfur functionality to prepare SF5-substituted heterocycles.

Grignard-Reagent-Promoted Desulfonylation/Intramolecular Coupling for the Synthesis of 2-(1-Fluorovinyl)pyridines

Jiang, Gaoxi,Kang, Lei,Qian, Jinlong,Yang, Huameng,Zhang, Jinlong

supporting information, p. 9118 - 9122 (2020/12/02)

A novel process involving Grignard-reagent-promoted desulfonylation/intramolecular coupling of readily available α-fluoro-α,β-unsaturated-(2-pyridyl)sulfones was realized that provided a series of polysubstituted 2-(1-fluorovinyl)pyridines in good yields. The intrinsic coordination between pyridine and Mg(II) along with the "negative fluorine effect"of the substrates should play the key role for the smooth transformation in the absence of transition-metal catalysts.

The Synthesis and Some Reactions of Novel Pyridine-2(1H)-thiones

Dunn, A. D.,Norrie, R.,L'Hostis, J.,Marjot, S.

, p. 119 - 125 (2007/10/02)

The use of methyl 3-mercaptopropionate for the conversion of halogenated pyridins to pyridine thiones and thiols is described, and limitations of the reaction discussed.S-Alkylation and oxidation reactions of the products from these reactions are reported.

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