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2-Naphthalenepropanenitrile, b-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

128104-64-3

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128104-64-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128104-64-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,1,0 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 128104-64:
(8*1)+(7*2)+(6*8)+(5*1)+(4*0)+(3*4)+(2*6)+(1*4)=103
103 % 10 = 3
So 128104-64-3 is a valid CAS Registry Number.

128104-64-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(naphthalen-2-yl)butanenitrile

1.2 Other means of identification

Product number -
Other names 3-(2-naphthalenyl)butyronitrile

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:128104-64-3 SDS

128104-64-3Downstream Products

128104-64-3Relevant academic research and scientific papers

Photocatalytic, Phosphoranyl Radical-Mediated N-O Cleavage of Strained Cycloketone Oximes

Xia, Peng-Ju,Ye, Zhi-Peng,Hu, Yuan-Zhuo,Song, Dan,Xiang, Hao-Yue,Chen, Xiao-Qing,Yang, Hua

, p. 2658 - 2662 (2019)

A photoinduced, phosphoranyl radical-mediated protocol for the direct N-O cleavage of strained cycloketone oximes via a polar/SET crossover process was developed for the first time. This visible-light-driven direct N-O activation mode for oxime offers beneficial features such as streamlined synthetic process and versatile photochemical reactivities. Consequently, the alkenes and α-trifluoromethyl alkenes with varied electronic and structural features acted as competent radical receptors in this protocol, enabling facile accesses to a range of elongated cyano and/or gem-difluoroalkene-bearing compounds.

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