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58324-82-6

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58324-82-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58324-82-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,3,2 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58324-82:
(7*5)+(6*8)+(5*3)+(4*2)+(3*4)+(2*8)+(1*2)=136
136 % 10 = 6
So 58324-82-6 is a valid CAS Registry Number.

58324-82-6SDS

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 4-(2-nitropropan-2-yl)benzonitrile

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:58324-82-6 SDS

58324-82-6Relevant articles and documents

CONCERNING THE MECHANISM OF DISPLACEMENT OF NITRO GROUPS FROM ACTIVATED AROMATIC SYSTEMS

Denney, Donald B.,Denney, Dorothy Z.,Perez, Airan Jun

, p. 4463 - 4476 (2007/10/02)

The photostimulated reactions of p-nitrobenzophenone and p-nitrobenzonitrile with a variety of nucleophiles have been investigated.Displacement of the nitro group is observed in all cases.The rates of the reactions were measured by FT-IR.The rates were slowed by substances such as sulfur, air, Galvinoxyl and p-benzoquinone.In several cases rates of loss of starting material were monitored by quenching the reaction mixtures and isolating product and starting material.These reactions also showed inhibition of their rates in the presence of inhibitors.These results indicate that the reactions are chain processes.It is concluded that the substrates are converted into their corresponding radical anions which then react with the nucleophiles in a bimolecular displacement reaction.The alternate mechanism, which involves dissociation of the radical anions, is precluded because they are known not to dissociate. Key words: Stable radical anions, nucleophilic displacements

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