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α,β-Diphenyl-β-(p-ethylphenyl)ethylene is a complex organic compound characterized by its unique molecular structure. It features a central ethylene (C=C) double bond, with two phenyl rings attached to the α and β carbons of the double bond. Additionally, a third phenyl ring is attached to the β carbon, which is substituted with an ethyl group at the para position. This arrangement of phenyl rings and the ethyl-substituted phenyl group endows the molecule with distinct chemical and physical properties, making it a potential candidate for various applications in the fields of materials science, pharmaceuticals, and organic chemistry. The compound's specific structure and properties can be further explored through experimental studies and computational modeling to understand its reactivity, stability, and potential interactions with other molecules.

86701-20-4

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86701-20-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86701-20-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,7,0 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86701-20:
(7*8)+(6*6)+(5*7)+(4*0)+(3*1)+(2*2)+(1*0)=134
134 % 10 = 4
So 86701-20-4 is a valid CAS Registry Number.

86701-20-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name α,β-diphenyl-β-(p-ethylphenyl)ethylene

1.2 Other means of identification

Product number -
Other names 1-(4-ethyl-phenyl)-1,2-diphenyl-ethene

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:86701-20-4 SDS

86701-20-4Relevant academic research and scientific papers

Palladium-catalyzed desulfitative hydroarylation of alkynes with sodium sulfinates

Liu, Saiwen,Bai, Yang,Cao, Xiangxiang,Xiao, Fuhong,Deng, Guo-Jun

supporting information, p. 7501 - 7503 (2013/08/23)

A palladium-catalyzed desulfitative hydroarylation of alkynes with aryl sulfinic acid sodium salts is described. The reaction showed good regio- and stereoselectivity, and afforded the hydroarylation products in good yields. Various functional groups were well tolerated under the optimized reaction conditions.

Synthesis of Broparestrol using Palladium-Catalyzed Cross-coupling

Al-Hassan, Mohammed I.

, p. 119 - 122 (2007/10/02)

The synthesis of broparestrol, a biologically active tetrasubstituted olefin used in dermatology, was achieved via palladium-catalyzed cross-coupling to form a C-C bond followed by bromination.Broparestrol (a cis-trans mixture of α-bromo-α,β-diphenyl-β-(p

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