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1-BROMO-4-(4-PHENYL-1,3-BUTADIENYL)BENZENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58922-30-8

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58922-30-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58922-30-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,9,2 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 58922-30:
(7*5)+(6*8)+(5*9)+(4*2)+(3*2)+(2*3)+(1*0)=148
148 % 10 = 8
So 58922-30-8 is a valid CAS Registry Number.

58922-30-8SDS

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 1-bromo-4-((1E,3E)-4-phenylbuta-1,3-dien-1-yl)benzene

1.2 Other means of identification

Product number -
Other names 1-bromo-4-((1E,3E)-4-phenylbuta-1,3-dienyl)benzene

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:58922-30-8 SDS

58922-30-8Relevant academic research and scientific papers

One-Pot Intermolecular Reductive Cross-Coupling of Deactivated Aldehydes to Unsymmetrically 1,2-Disubstituted Alkenes

Arkhypchuk, Anna I.,D'Imperio, Nicolas,Ott, Sascha

supporting information, p. 5086 - 5089 (2018/09/13)

The phospha-Peterson reaction between a lithiated secondary phosphane, MesP(Li)TMS, and an aldehyde affords Mes-phosphaalkenes which, upon methanol addition and P-oxidation, react with a second carbonyl compound site specifically to produce unsymmetric alkenes. The E/Z selectivity of the one-pot cross coupling is largely determined by the electronic nature of the aryl substituent of the first aldehyde, with electron-donating groups giving rise to increased amounts of Z-alkenes.

Divergent rearrangements of cyclopropyl-substituted fluoroepoxides involving c-f bond cleavage and formation

Luo, Tao,Zhang, Rui,Zhang, Wei,Shen, Xiao,Umemoto, Teruo,Hu, Jinbo

supporting information, p. 888 - 891 (2014/03/21)

Unprecedented divergent rearrangements of cyclopropyl-substituted fluoroepoxides are reported. In the presence of a catalytic amount of benzoic acid, cyclopropyl-substituted fluoroepoxides efficiently undergo 1,5-fluorine migration. However, when the fluo

Syntheses of p-terphenyls and 11,12-dihydroindeno[2,1-a]fluorene by one-pot benzannulation of Diels-Alder reactions of trans-1,2-dichloroethene and dienes

Ho, Jinn-Hsuan,Lin, Yu-Chen,Chou, Li-Ting,Chen, Ying-Zhe,Liu, Wei-Qi,Chuang, Chao-Li

, p. 1991 - 1993 (2013/04/10)

A series of substituted p-terphenyls and 11,12-dihydroindeno[2,1-a]fluorene were successfully synthesized by one-pot benzannulation of Diels-Alder reaction with 1,2-dichloroethene as an acetylene equivalent dienophile. Two chlorine atoms could be good leaving groups to easily undergo subsequent elimination reactions of Diels-Alder products at a high temperature.

Cyclic 1,1-bis(silyl)alkenes-new building blocks for the stereoselective synthesis of unsymmetrical (E)-stilbenes and (E,E)-1,4-diarylbuta-1,3-dienes

Pawlu?, Piotr,Hreczycho, Grzegorz,Suchecki, Andrzej,Kubicki, Maciej,Marciniec, Bogdan

experimental part, p. 5497 - 5502 (2009/12/03)

A new efficient synthetic protocol for the highly stereoselective synthesis of unsymmetrical (or symmetrical) (E)-stilbenes and (E,E)-1,4-diarylbuta-1,3-dienes based on sequential palladium-catalyzed Heck arylation-Hiyama cross-coupling reactions using cy

Palladium-catalyzed stereoselective synthesis of (E)-stilbenes via organozinc reagents and carbonyl compounds

Wang, Jin-Xian,Wang, Kehu,Zhao, Lianbiao,Li, Hongxia,Fu, Ying,Hu, Yulai

, p. 1262 - 1270 (2007/10/03)

In the presence of a catalytic amount of PdCl2(PPh 3)2 and a silylating agent, organozinc halides reacted with carbonyl compounds to give the corresponding (E)-stilbenes in good to excellent yields under mild conditions. The reaction mechanism is briefly discussed.

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