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3678-63-5

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3678-63-5 Usage

Chemical Properties

Light yellow liquid

Uses

4-Chloro-2-picoline (cas# 3678-63-5) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 3678-63-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,7 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3678-63:
(6*3)+(5*6)+(4*7)+(3*8)+(2*6)+(1*3)=115
115 % 10 = 5
So 3678-63-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H6ClN/c1-5-4-6(7)2-3-8-5/h2-4H,1H3

3678-63-5 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Detail
  • Alfa Aesar

  • (H64093)  4-Chloro-2-methylpyridine, 95%   

  • 3678-63-5

  • 1g

  • 527.0CNY

  • Detail
  • Alfa Aesar

  • (H64093)  4-Chloro-2-methylpyridine, 95%   

  • 3678-63-5

  • 5g

  • 1980.0CNY

  • Detail
  • Alfa Aesar

  • (H64093)  4-Chloro-2-methylpyridine, 95%   

  • 3678-63-5

  • 25g

  • 7899.0CNY

  • Detail

3678-63-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chloro-2-methylpyridine

1.2 Other means of identification

Product number -
Other names 4-Chloro-2-Methylpyridine

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:3678-63-5 SDS

3678-63-5Relevant articles and documents

Chemoselective sp 2-sp3 cross-couplings: Iron-catalyzed alkyl transfer to dihaloaromatics

Malhotra, Sushant,Seng, Pamela S.,Koenig, Stefan G.,Deese, Alan J.,Ford, Kevin A.

supporting information, p. 3698 - 3701 (2013/08/23)

The chemoselective functionalization of a range of dihaloaromatics with methyl, cyclopropyl, and higher alkyl Grignard reagents via iron-catalyzed cross-coupling is described. The site selectivity of C-X (X = halogen) activation is determined by factors such as the position of the halogen on the ring, the solvent, and the nucleophile. A one-pot protocol for the chemoselective synthesis of mixed dialkyl heterocycles is achieved solely employing iron catalysis.

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