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Cyclohexanone, 2-(2-chloro-3-pyridinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

823787-29-7

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823787-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 823787-29-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,3,7,8 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 823787-29:
(8*8)+(7*2)+(6*3)+(5*7)+(4*8)+(3*7)+(2*2)+(1*9)=197
197 % 10 = 7
So 823787-29-7 is a valid CAS Registry Number.

823787-29-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-chloropyridin-3-yl)cyclohexan-1-one

1.2 Other means of identification

Product number -
Other names Cyclohexanone,2-(2-chloro-3-pyridinyl)

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:823787-29-7 SDS

823787-29-7Relevant academic research and scientific papers

Palladium-catalyzed intramolecular O-arylation of enolates: Application to benzo[6]furan synthesis

Willis, Michael C.,Taylor, Dawn,Gillmore, Adam T.

, p. 4755 - 4757 (2004)

(Chemical Equation Presented) A catalyst generated from Pd 2(dba)3 and the ligand DPEphos effects intramolecular C-O bond formation between enolates and aryl halides in the conversion of 1-(2-haloaryl)ketones directly into the corres

Palladium-catalyzed tandem alkenyl and aryl C-N bond formation: A cascade N-annulation route to 1-functionalized indoles

Willis, Michael C.,Brace, Gareth N.,Holmes, Ian P.

, p. 403 - 406 (2007/10/03)

(Chemical Equation Presented) A single tandem operation allows rapid access to a variety of substituted N-functionalized indoles. The nitrogen atom of the indole nucleus is incorporated through Pd-catalyzed aryl and alkenyl C-N bond-forming reactions (see scheme; dba = dibenzylideneacetone). Amine, aniline, amide, carbamate, and sulfonamide functional groups can be introduced efficiently.

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