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

35861-33-7

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35861-33-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35861-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,8,6 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 35861-33:
(7*3)+(6*5)+(5*8)+(4*6)+(3*1)+(2*3)+(1*3)=127
127 % 10 = 7
So 35861-33-7 is a valid CAS Registry Number.

35861-33-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4'-dimethoxybenzophenone radical

1.2 Other means of identification

Product number -
Other names -

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:35861-33-7 SDS

35861-33-7Downstream Products

35861-33-7Relevant academic research and scientific papers

Kinetic study of the hydrogen abstraction reaction of the benzotriazole-N-oxyl radical (BTNO) with H-donor substrates

Brandi, Paolo,Galli, Carlo,Gentili, Patrizia

, p. 9521 - 9528 (2007/10/03)

The aminoxyl radical (>N-O.) BTNO (benzotriazole-N-oxyl) has been generated by the oxidation of 1-hydroxybenzotriazole (HBT; >N-OH) with a CeIV salt in MeCN. BTNO presents a broad absorption band with λmax 474 nm and e 184

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.

Direct measurement of ultrafast carbon-carbon cleavage rates via the subpicosecond charge-transfer activation of pinacols

Bockman,Hubig,Kochi

, p. 6542 - 6547 (2007/10/03)

Highly transient (benzpinacol) cation radicals (D2+.) and their ultrafast mesolytic fragmentations to the diarylhydroxymethyl radical (D.) and cation (D+) are directly observed on the early picosecond time scale upon the charge-transfer photoactivation of the intermolecular donor-acceptor complexes of pinacol donors with methyl viologen. Ultrashort lifetimes of the cation radicals with τ ~ 10 ps obtain (for the first time) from quantitative kinetics analysis of the time-resolved spectroscopic results. These rapid C-C bond scissions successfully compete with back-electron transfer, which normally predominates on this time scale, and lead to exceptionally high efficiencies for the oxidative fragmentation of pinacols.

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