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63459-07-4

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63459-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63459-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,4,5 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 63459-07:
(7*6)+(6*3)+(5*4)+(4*5)+(3*9)+(2*0)+(1*7)=134
134 % 10 = 4
So 63459-07-4 is a valid CAS Registry Number.

63459-07-4SDS

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 N-benzylprop-2-en-1-imine

1.2 Other means of identification

Product number -
Other names Benzenemethanamine,N-2-propenylidene

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:63459-07-4 SDS

63459-07-4Relevant articles and documents

Electro-Mechanochemical Atom Transfer Radical Cyclizations using Piezoelectric BaTiO3

Bolm, Carsten,Hernández, José G.,Schumacher, Christian

, p. 16357 - 16360 (2020)

The formation and regeneration of active CuI species is a fundamental mechanistic step in copper-catalyzed atom transfer radical cyclizations (ATRC). Typically, the presence of the catalytically active CuI species in the reaction mix

Asymmetric synthesis of Sedum alkaloids via lithium amide conjugate addition

Davies, Stephen G.,Fletcher, Ai M.,Roberts, Paul M.,Smith, Andrew D.

supporting information; experimental part, p. 10192 - 10213 (2010/02/28)

Conjugate addition of lithium (R)-N-allyl-N-(α-methylbenzyl)amide or lithium (R)-N-but-3-enyl-N-(α-methylbenzyl)amide to an alkyl hexa-2,4-dienoate or alkyl hepta-2,6-dienoate, followed by ring-closing metathesis of the olefin functionalities within the resultant β-amino ester, generates a range of diastereoisomerically pure azacycles in good yield. These homochiral templates are readily transformed to a range of piperidine alkaloids of the Sedum family, and the corresponding five-, seven- and eight-membered ring homologues.

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