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Methylene, (4-cyanophenyl)phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64568-30-5

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64568-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64568-30-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,5,6 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 64568-30:
(7*6)+(6*4)+(5*5)+(4*6)+(3*8)+(2*3)+(1*0)=145
145 % 10 = 5
So 64568-30-5 is a valid CAS Registry Number.

64568-30-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-cyanophenyl)phenylmethylene

1.2 Other means of identification

Product number -
Other names 4-Benzyl-benzonitrile

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:64568-30-5 SDS

64568-30-5Downstream Products

64568-30-5Relevant academic research and scientific papers

The Absolute Kinetics of Several Reactions of Substituted Diphenylcarbenes

Hadel, L. M.,Maloney, V. M.,Platz, M. S.,McGimpsey, W. G.,Scaiano, J. C.

, p. 2488 - 2491 (2007/10/02)

4,4'-dibromo-, 4-bromo-, 4,4'-dichloro-, 4-chloro-, 4-methyl-, 4,4'-dimethyl-, 4-phenyl-, 4-carbomethoxyl-, 4-cyano-, 4-cyano-4'-methyl-, and 4,4'-dimethyldiphenyldiazomethane were studied by laser flash photolysis.Excitation of the diazo compounds at 308 nm produced the corresponding diarylcarbenes.The kinetics of the reaction of the substituted carbenes with alkanes and methanol were examined.Hydrogen abstraction rates are largely insensitive to ring substitution, while the methanol reaction is accelerated considerably by p-methyl substitution and retarded by a para electron-withdrawing substituent.

Photophysics of Some Substituted Diphenylmethylenes

Ono, Y.,Ware, W. R.

, p. 4426 - 4433 (2007/10/02)

Absorption, emission, and excitation spectra, fluorescence decay times, and quantum yields of a series of substituted diphenylmethylenes have been measured in various rigid organic matrices at low temperatures.Substitution on the phenyl ring led to a decrease in lifetime, the greatest effect being observed in the dibromo compound, the lifetime of which was 10percent that of the unsubstituted compound.In addition, there was a small but noticeable external heavy atom effect on the decay times.The fluorescence quantum yields of some of the substituted diphenylmethylenes were found to depend on the energy of excitation.Changes in the absorption spectra in the temperature range between 4 and 95 K may be the result of appreciable population of close-lying singlet and triplet levels in the ground state at 95 K.The spectral changes were irreversible, however, possibly implying geometrical configuration changes.

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