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18368-64-4

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18368-64-4 Usage

Description

2-Chloro-5-methylpyridine is an organic compound that serves as a crucial intermediate in the synthesis of various chemical products. It is characterized by its clear light yellow to straw-yellow liquid appearance and holds significance in the chemical and pharmaceutical industries due to its versatile reactivity and potential applications.

Uses

Used in Chemical Synthesis:
2-Chloro-5-methylpyridine is used as a key intermediate for the synthesis of several chemical compounds, including:
2-methylthio-5-pyridinemethylene amine, which may have applications in the development of pharmaceuticals or other specialty chemicals.
5-methyl-2,2′-bipyridine, a compound that could be utilized in the creation of complex organic molecules or materials with specific properties.
1-(5′-methyl-2,2′-bipyridin-5-yl)-2,5-dimethyl-1H-pyrrole, which might be employed in the production of novel chemical entities with potential applications in various fields.
Used in Pesticide Industry:
2-Chloro-5-methylpyridine is also used as a pesticide intermediate, playing a vital role in the development of new pesticides to protect crops and enhance agricultural productivity. Its chemical properties make it a valuable component in the formulation of effective and targeted pest control solutions.

Check Digit Verification of cas no

The CAS Registry Mumber 18368-64-4 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, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18368-64:
(7*1)+(6*8)+(5*3)+(4*6)+(3*8)+(2*6)+(1*4)=134
134 % 10 = 4
So 18368-64-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H6ClN/c1-5-2-3-6(7)8-4-5/h2-4H,1H3

18368-64-4 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H59145)  2-Chloro-5-methylpyridine, 97%   

  • 18368-64-4

  • 5ml

  • 286.0CNY

  • Detail
  • Alfa Aesar

  • (H59145)  2-Chloro-5-methylpyridine, 97%   

  • 18368-64-4

  • 25ml

  • 1018.0CNY

  • Detail
  • Aldrich

  • (495328)  2-Chloro-5-methylpyridine  97%

  • 18368-64-4

  • 495328-5ML

  • 524.16CNY

  • Detail
  • Aldrich

  • (495328)  2-Chloro-5-methylpyridine  97%

  • 18368-64-4

  • 495328-25ML

  • 1,788.93CNY

  • Detail

18368-64-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-5-methylpyridine

1.2 Other means of identification

Product number -
Other names 6-CHLORO-3-PICOLINE

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:18368-64-4 SDS

18368-64-4Relevant articles and documents

Convenient access to new chiral ferroceno-(iso)quinolines

Mamane, Victor,Fort, Yves

, p. 8220 - 8223 (2005)

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Efficient Phosphorus-Free Chlorination of Hydroxy Aza-Arenes and Their Application in One-Pot Pharmaceutical Synthesis

Wang, Jian,Li, Yan-Hui,Pan, Song-Cheng,Li, Ming-Fang,Du, Wenting,Yin, Hong,Li, Jing-Hua

supporting information, p. 146 - 153 (2020/03/10)

The chlorination of hydroxy aza-arenes with bis(trichloromethyl) carbonate (BTC) and SOCl2 has been effectively performed by refluxing with 5 wt % 4-dimethylaminopyridine (DMAP) as a catalyst. Various substrates are chlorinated with high yields. The obtained chlorinated aza-arenes can be used directly with simple workup for succedent one-pot synthesis on a large scale.

Transition-metal-free decarboxylative halogenation of 2-picolinic acids with dihalomethane under oxygen conditions

Zhang, Xitao,Feng, Xiujuan,Zhang, Haixia,Yamamoto, Yoshinori,Bao, Ming

supporting information, p. 5565 - 5570 (2019/10/22)

A convenient and efficient method for the synthesis of 2-halogen-substituted pyridines is described. The decarboxylative halogenation of 2-picolinic acids with dihalomethane proceeded smoothly via N-chlorocarbene intermediates to afford 2-halogen-substituted pyridines in satisfactory to excellent yields under transition-metal-free conditions. This new type of decarboxylative halogenation is operationally simple and exhibits high functional-group tolerance.

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