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1-Benzyl-4-hydroxy-3-phenethyl-4,5-diphenyl-pyrrolidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106875-35-8

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106875-35-8 Usage

Chemical structure

A complex structure consisting of a pyrrolidin-2-one ring with a benzyl group, a hydroxy group, and three phenethyl and diphenyl groups attached to it.

Classification

A type of phenylpiperidines, which are a class of psychoactive substances.

Natural occurrence

Not commonly found in nature.

Synthesis

May be synthesized in a laboratory.

Pharmacological properties

Has been studied for its potential effects on the central nervous system.

Specific uses

Not well-documented, but the chemical structure suggests it may have psychoactive and potentially pharmacological properties.

Potential risks

Not well-documented, but further research is needed to understand its effects and potential applications.

Research status

Further research is needed to fully understand its effects, potential applications, and risks.

Check Digit Verification of cas no

The CAS Registry Mumber 106875-35-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,8,7 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 106875-35:
(8*1)+(7*0)+(6*6)+(5*8)+(4*7)+(3*5)+(2*3)+(1*5)=138
138 % 10 = 8
So 106875-35-8 is a valid CAS Registry Number.

106875-35-8Downstream Products

106875-35-8Relevant academic research and scientific papers

Photocyclisation of NN-Dialkyl β,γ-Unsaturated Amides. 1,6-Hydrogen Transfer via Charge-transfer States

Aoyama, Hiromu,Arata, Yoshiaki,Omote, Yoshimori

, p. 1165 - 1170 (2007/10/02)

NN-dibenzyl and NN-diallyl β,γ-unsaturated amides undergo cyclization on irradiation to give the corresponding pyrrolidin-2-ones via 1,6-hydrogen transfer from the singlet states.The reaction is presumed to involve charge transfer from the amide group to

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