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63462-63-5

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63462-63-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63462-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,4,6 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 63462-63:
(7*6)+(6*3)+(5*4)+(4*6)+(3*2)+(2*6)+(1*3)=125
125 % 10 = 5
So 63462-63-5 is a valid CAS Registry Number.

63462-63-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name p-(1-isopropylamino-1-methylethyl)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:63462-63-5 SDS

63462-63-5Downstream Products

63462-63-5Relevant articles and documents

Photochemical Reactions of Dicyanobenzenes with Aliphatic Amines

Ohashi, Mamoru,Miyake, Kentaro,Tsujimoto, Kazuo

, p. 1683 - 1688 (2007/10/02)

Upon irradiation, p-dicyanobenzene reacted with primary, secondary, and tertiary aliphatic amines to give substitution products in which one of the cyano groups was replaced by the amine at α-CH position or by an alkyl group of the amine. o-Dicyanobenzene reacted similarly, but the meta-isomer did not react under similar conditions.The rates of the fluorescence quenching of p-dicyanobenzene with the amines are close to the diffusion-controlled rate, but are somewhat dependent on the ionization potentials of the amines.When the substitution product was irradiated, the cor responding alkylation product was obtained.The mechanism of these reactions have been investigated by the use of such proton donors as MeOH(MeOD); on the basis of those investigations, new photochemical reactions involving charge-transfer, followed by proton-transfer and then addition-elimination, are proposed, as well as a new type of photo-induced Birch reduction

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