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Methyl, hydroxy(4-methylphenyl)phenyl-, a phenol derivative with the molecular formula C15H16O, is a chemical compound featuring a hydroxy and a methyl group attached to a benzene ring. This unique structure endows it with distinctive properties and makes it a valuable intermediate in organic chemistry, particularly in the synthesis of pharmaceuticals and agrochemicals.

145191-23-7

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145191-23-7 Usage

Uses

Used in Pharmaceutical Industry:
Methyl, hydroxy(4-methylphenyl)phenylis used as an intermediate in the synthesis of various pharmaceuticals for its potential to contribute to the development of new drugs with unique therapeutic properties.
Used in Agrochemical Industry:
Methyl, hydroxy(4-methylphenyl)phenylis utilized as a building block in the production of agrochemicals, such as pesticides and herbicides, due to its ability to enhance the effectiveness and selectivity of these compounds.
Used in Organic Chemistry Research:
As a versatile intermediate, Methyl, hydroxy(4-methylphenyl)phenylis employed in organic chemistry research for the synthesis of complex organic molecules, contributing to the advancement of chemical science and the discovery of novel applications.

Check Digit Verification of cas no

The CAS Registry Mumber 145191-23-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,1,9 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 145191-23:
(8*1)+(7*4)+(6*5)+(5*1)+(4*9)+(3*1)+(2*2)+(1*3)=117
117 % 10 = 7
So 145191-23-7 is a valid CAS Registry Number.

145191-23-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methylbenzophenone radical

1.2 Other means of identification

Product number -
Other names PHENYL(P-TOLYL)METHANOL

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:145191-23-7 SDS

145191-23-7Downstream Products

145191-23-7Relevant academic research and scientific papers

Triplet Quenching by tert-Butyl Hydroperoxide

Stewart, Laura C.,Carlsson, D. J.,Wiles, D. M.,Scainano, J. C.

, p. 3605 - 3609 (1983)

Laser flash photolysis studies show that tert-butyl hydroperoxide is an excellent quencher.For example, the rate constants for benzophenone and phenanthrene in benzene at 300 K are 1.8 x 108 and 2.3 x 107 M-1 s-1/sup

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.

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