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118578-71-5

118578-71-5

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118578-71-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118578-71-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,5,7 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 118578-71:
(8*1)+(7*1)+(6*8)+(5*5)+(4*7)+(3*8)+(2*7)+(1*1)=155
155 % 10 = 5
So 118578-71-5 is a valid CAS Registry Number.

118578-71-5 Well-known Company Product Price

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  • Aldrich

  • (78166)  N-(4-Phenylbenzylidene)benzylamine  ≥98.0% (GC)

  • 118578-71-5

  • 78166-1G

  • 1,171.17CNY

  • Detail

118578-71-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-1-(4-phenylphenyl)methanimine

1.2 Other means of identification

Product number -
Other names 1-(biphenyl-4-yl)-3-phenyl-2-azapropene

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:118578-71-5 SDS

118578-71-5Relevant articles and documents

4-Phenylbenzylidene benzylamine: a new and convenient reagent for the titration of solutions of lithium alkyls and metal amides

Duhamel, Lucette,Plaquevent, Jean-Christophe

, p. 1 - 3 (1993)

4-Phenylbenzylidene benzylamine is shown to be an excellent reagent for the determination of solutions of lithium alkyls and metal amides.The azaallyl anion produced is deep blue in tetrahydrofuran, and fades to pale yellow via red when titrated with 2-bu

Oxidation of N-benzylaldimines to N-benzylamides by MCPBA and BF3·OEt2

An, Gwang-Il,Rhee, Hakjune

, p. 876 - 878 (2007/10/03)

N-Benzylamides were obtained from the corresponding N-benzylaldimines in high yields. N-Benzylaldimines are readily prepared from the corresponding aldehydes with benzylamine. This procedure involves the oxidation of N-benzylaldimines with MCPBA with BF3·OEt2. In this reaction, the reaction presumably follows an internal hydrogen abstraction to provide only N-benzylamide.

Thermal and Photoisomerisation of Ion Pairs of the 1,3-Diphenyl-2-aza-allyl Carbanion

Young, Ronald N.,Ahmad, Muhanad A.

, p. 35 - 38 (2007/10/02)

Upon irradiation with white light, the predominant conformation of the 1,3-diphenyl-2-aza-allyl carbanion is changed from trans, trans to cis, trans.The kinetics of the reverse dark reaction have been studied.The loose ion pairs with lithium, sodium, and

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