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5-(3-CHLOROPHENYL)-5-OXOVALERONITRILE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

898767-68-5

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898767-68-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 898767-68-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,7,6 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 898767-68:
(8*8)+(7*9)+(6*8)+(5*7)+(4*6)+(3*7)+(2*6)+(1*8)=275
275 % 10 = 5
So 898767-68-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H10ClNO/c12-10-5-3-4-9(8-10)11(14)6-1-2-7-13/h3-5,8H,1-2,6H2

898767-68-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(3-chlorophenyl)-5-oxopentanenitrile

1.2 Other means of identification

Product number -
Other names 5-(3-CHLOROPHENYL)-5-OXOVALERONITRILE

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:898767-68-5 SDS

898767-68-5Upstream product

898767-68-5Downstream Products

898767-68-5Relevant academic research and scientific papers

Nickel-Catalyzed Reductive Electrophilic Ring Opening of Cycloketone Oxime Esters with Aroyl Chlorides

Ding, Decai,Wang, Chuan

, p. 11324 - 11329 (2018)

By merging cross-electrophile coupling and C-C bond cleavage, we developed a Ni-catalyzed electrophilic ring opening of cycloketone oxime esters with aromatic acid chlorides in assistance of Mn as reductant. Notably, complete regioselectivity can be achieved in this C-C bond cleavage reaction, providing an efficient access to a variety of cyanoketones under cyanide-free conditions. A radical reaction pathway was proposed on the basis of the results of the mechanistic probing experiments.

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