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6-(2-METHOXYPHENYL)-6-OXOHEXANENITRILE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

898786-52-2

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898786-52-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 898786-52-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,7,8 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 898786-52:
(8*8)+(7*9)+(6*8)+(5*7)+(4*8)+(3*6)+(2*5)+(1*2)=272
272 % 10 = 2
So 898786-52-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H15NO2/c1-16-13-9-5-4-7-11(13)12(15)8-3-2-6-10-14/h4-5,7,9H,2-3,6,8H2,1H3

898786-52-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(2-Methoxyphenyl)-6-oxohexanenitrile

1.2 Other means of identification

Product number -
Other names -

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:898786-52-2 SDS

898786-52-2Upstream product

898786-52-2Downstream Products

898786-52-2Relevant academic research and scientific papers

A photoredox catalyzed iminyl radical-triggered C-C bond cleavage/addition/Kornblum oxidation cascade of oxime esters and styrenes: synthesis of ketonitriles

He, Bin-Qing,Yu, Xiao-Ye,Wang, Peng-Zi,Chen, Jia-Rong,Xiao, Wen-Jing

, p. 12262 - 12265 (2018)

A photoredox-catalyzed iminyl radical-triggered C-C bond cleavage/addition/Kornblum oxidation cascade of cycloketone oxime esters and styrenes in DMSO is described. This three-component, one-pot procedure features mild conditions, a broad substrate scope, and high functional group tolerance, providing an efficient approach to access diversely functionalized ketonitriles.

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