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Methyl, bis(4-chlorophenyl)hydroxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91150-43-5

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91150-43-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91150-43-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,1,5 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 91150-43:
(7*9)+(6*1)+(5*1)+(4*5)+(3*0)+(2*4)+(1*3)=105
105 % 10 = 5
So 91150-43-5 is a valid CAS Registry Number.

91150-43-5SDS

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 4,4'-dichlorobenzophenone ketyl radical

1.2 Other means of identification

Product number -
Other names 4,4'-dichlorobenzophenone radical

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:91150-43-5 SDS

91150-43-5Downstream Products

91150-43-5Relevant academic research and scientific papers

Picosecond Dynamics of Nonadiabatic Proton Transfer: A Kinetic Study of Proton Transfer within the Contact Radical Ion Pair of Substituted Benzophenones/N,N-Dimethylaniline

Peters, Kevin S.,Cashin, Amanda,Timbers, Peter

, p. 107 - 113 (2007/10/03)

Picosecond absorption spectroscopy has been employed in the study of the dynamics of proton transfer within substituted benzophenones/N,N-dimethylaniline contact radical ion pairs. The reactions were investigated in the solvents cyclohexane, benzene, and dimethylformamide. The correlation of the reaction rates with the change in free energy reveals that the reaction pathway corresponds to a nonadiabatic process, that is the reaction proceeds by proton tunneling. In nonpolar solvents, an inverted region is observed in the proton-transfer process.

Picosecond Dynamics of Proton Transfers

Manring, Lewis E.,Peters, Kevin S.

, p. 6452 - 6458 (2007/10/02)

The dynamics of proton transfer within an acid-base pair, which is created by a photoinduced electron transfer from an amine to a ketone, is investigated through picosecond absorption spectroscopy.Questions relating to molecular motion within the encounter complex and the distance dependence of proton transfer are addressed.Specifically, for substituted benzophenones and diphenylmethylamine, isotope and solvent dependence studies reveal that, although an acid-base pair is formed as an encounter complex, prior reorientation within the complex must take place before proton transfer.Other systems investigated include the transfer of a proton from the radical cation of N-methylacridan to the radical anions of benzophenone and anthraquinone as well as an intramolecular proton transfer for a molecule containing dimethylaniline linked to benzophenone by a methylene bridge.

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