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Benzeneacetonitrile, a-butyl-2-chloro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58830-36-7

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58830-36-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58830-36-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,8,3 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58830-36:
(7*5)+(6*8)+(5*8)+(4*3)+(3*0)+(2*3)+(1*6)=147
147 % 10 = 7
So 58830-36-7 is a valid CAS Registry Number.

58830-36-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-Chloro-phenyl)-hexanenitrile

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:58830-36-7 SDS

58830-36-7Downstream Products

58830-36-7Relevant academic research and scientific papers

Sustainable Alkylation of Nitriles with Alcohols by Manganese Catalysis

Borghs, Jannik C.,Tran, Mai Anh,Sklyaruk, Jan,Rueping, Magnus,El-Sepelgy, Osama

, p. 7927 - 7935 (2019/06/24)

A general and chemoselective catalytic alkylation of nitriles using a homogeneous nonprecious manganese catalyst is presented. This alkylation reaction uses naturally abundant alcohols and readily available nitriles as coupling partners. The reaction tolerates a wide range of functional groups and heterocyclic moieties, efficiently providing useful cyanoalkylated products with water as the only side product. Importantly, methanol can be used as a C1 source and the chemoselective C-methylation of nitriles is achieved. The mechanistic investigations support the multiple role of the metal-ligand manganese catalyst, the dehydrogenative activation of the alcohol, α-C-H activation of the nitrile, and hydrogenation of the in-situ-formed unsaturated intermediate.

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