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Benzene, 1,1'-(1,4-cyclohexadiene-1,4-diyl)bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66241-48-3

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66241-48-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66241-48-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,4 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 66241-48:
(7*6)+(6*6)+(5*2)+(4*4)+(3*1)+(2*4)+(1*8)=123
123 % 10 = 3
So 66241-48-3 is a valid CAS Registry Number.

66241-48-3SDS

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 1,4-Diphenyl-cyclohexa-1,4-diene

1.2 Other means of identification

Product number -
Other names 1,4-Diphenyl-cyclohexadien-1,4

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:66241-48-3 SDS

66241-48-3Relevant academic research and scientific papers

Nickel-Catalyzed Direct Synthesis of Aryl Olefins from Ketones and Organoboron Reagents under Neutral Conditions

Lei, Chuanhu,Yip, Yong Jie,Zhou, Jianrong Steve

supporting information, p. 6086 - 6089 (2017/05/08)

Nickel-catalyzed addition of arylboron reagents to ketones results in aryl olefins directly. The neutral condition allows acidic protons of alcohols, phenols, and malonates to be present, and fragile structures are also tolerated.

Striking Contrast between Photoinduced and Non-photoinduced Electron-transfer Reactions of 1,4-Diphenyl-2,3-diazabicyclooct-2-ene

Ikeda, Hiroshi,Minegishi, Tomonori,Miyashi, Tsutomu

, p. 297 - 298 (2007/10/02)

Photoinduced electron-transfer (PET) reactions of 1,4-diphenyl-2,3-diazabicyclooct-2-ene 1 result in a quantitative formation of 2,5-diphenylhexa-1,5-diene 2, in sharp contrast to the results of non-PET reactions and showing the importance of a back electron-transfer (BET) process in PET reactions.

Model Substances for Electro-optical and Dielectric Studies, Part I. Synthesis and Structure of 1,4-Bis(4'-dimethylamino-3',5'-dicyanophenyl)bicyclooctane

Detzer, Norbert,Burkhard, Oswald,Schaffrin, Heinz,Liptay, Wolfgang

, p. 1129 - 1141 (2007/10/02)

A synthesis for a new 1,2,6-donor-acceptor-substituted chromophoric benzene system is given.This chromophore is incorporated in a bicyclooctane system to build up model compounds for electro-optical and dielectrical studies.Furthermore a preparative convenient route to derivatives of 1,4-bis(diphenyl)bicyclooctane is worked out.The structures of the new compounds are proven by spectroscopical means. - Key words: 1,2,6-Donor-Acceptor-Substituted Benzenes, 1,4-Bis(diphenyl)bicyclooctane Derivatives

SYNTHESIS OF 1,4-DISUBSTITUTED BICYCLOOCTANES BY THE DIELS-ALDER REACTION

Geivandov, R.Kh.,Kovshev, E.I.

, p. 461 - 470 (2007/10/02)

Methods were developed for the synthesis of 1,4-diethoxy-, 1,4-dicyano-, and 1,4-diphenyl-1,3-cyclohexadienes.Their adducts with maleic anhydride, acrylonitrile, acrolein, nitroethylene, fumaronitrile, and α-acetoacrylonitrile were converted into the corresponding substituted bicyclooctanes.The configuration of the diene synthesis products was studied by IR and PMR spectroscopy.

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