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13382-54-2

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13382-54-2 Usage

General Description

2-Chloro-6-phenylpyridine is a chemical compound with the molecular formula C11H8ClN. It is a pyridine derivative with a chlorine atom at the 2-position and a phenyl group at the 6-position. 2-CHLORO-6-PHENYLPYRIDINE is primarily used in the pharmaceutical industry as a building block for the synthesis of various biologically active molecules, such as pharmaceutical drugs and agrochemicals. It has also been studied for its potential as a ligand in coordination chemistry and for its biological activity in various cellular pathways. 2-Chloro-6-phenylpyridine is considered to be a valuable intermediate in organic synthesis and has potential applications in both the pharmaceutical and chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 13382-54-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,8 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13382-54:
(7*1)+(6*3)+(5*3)+(4*8)+(3*2)+(2*5)+(1*4)=92
92 % 10 = 2
So 13382-54-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H8ClN/c12-11-8-4-7-10(13-11)9-5-2-1-3-6-9/h1-8H

13382-54-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-6-phenylpyridine

1.2 Other means of identification

Product number -
Other names 2-chloro-6-phenyl-pyridine

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:13382-54-2 SDS

13382-54-2Relevant articles and documents

Direct Synthesis of Benzoylpyridines from Chloropyridines via a Palladium-Carbene Catalyzed Carbonylative Suzuki Cross-Coupling Reaction

Maerten, Eddy,Hassouna, Fatima,Couve-Bonnaire, Samuel,Mortreux, André,Carpentier, Jean-Fran?ois,Castanet, Yves

, p. 1874 - 1876 (2003)

The use of N-heterocyclic carbene-type ligands with palladium catalysts allows the activation of chloropyridines and chloroquinoline towards carbonylative cross-coupling with phenylboronic acid for the synthesis of unsymmetrical biaryl ketones.

Micelle-Enabled Suzuki-Miyaura Cross-Coupling of Heteroaryl Boronate Esters

Guo, Pengfei,Zhang, Hao,Zhou, Jianguang,Gallou, Fabrice,Parmentier, Michael,Wang, Hui

, p. 7523 - 7527 (2018/06/04)

We report a micellar protocol for Suzuki-Miyaura cross-coupling of heteroaryl boronic esters with aryl or heteroaryl halides. The micellar catalysis enables this coupling reaction to run under mild conditions, which avoids the decomposition of heteroaryl boronate esters and allows for high chemoselectivity for cross-coupling reaction with 6-chloropridine-2-boronic ester. The micellar protocol expands the scope of the cross-coupling reaction with challenging heteroaryl boronic esters and complements the existing cross-coupling methods for construction of heterobiaryl building blocks.

Cross-coupling study of iodo/chloropyridines and 2-chloroquinoline with atom-economic triarylbismuth reagents under Pd-catalysis

Rao, Maddali L.N.,Dhanorkar, Ritesh J.

, p. 338 - 349 (2015/03/04)

This study describes the palladium-catalyzed couplings of iodopyridines, chloropyridines, and chloroquinoline with atom-economic BiAr3 reagents in sub-stoichiometric loadings. Mono-arylations of iodo and chloropyridines produced arylpyridines i

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