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Benzene, 1-bromo-4-(1-phenylethenyl)-, also known as 1-bromo-4-(1-phenylprop-1-en-1-yl)benzene or 4-(1-phenylprop-1-en-1-yl)bromobenzene, is an organic compound with the molecular formula C??H??Br. It is a derivative of benzene, featuring a bromine atom at the 1-position and a phenylpropenyl group at the 4-position. Benzene, 1-bromo-4-(1-phenylethenyl)- is characterized by its aromatic structure and the presence of a vinyl group, which contributes to its chemical reactivity. It is used in various chemical syntheses, particularly in the production of pharmaceuticals and other organic compounds. Due to its bromine content, it can be involved in substitution reactions, and the vinyl group allows for further functionalization. The compound is typically handled with care due to its potential reactivity and the need to manage bromine, which can be toxic.

4333-76-0

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4333-76-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4333-76-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,3 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4333-76:
(6*4)+(5*3)+(4*3)+(3*3)+(2*7)+(1*6)=80
80 % 10 = 0
So 4333-76-0 is a valid CAS Registry Number.

4333-76-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-4-(1-phenylethenyl)benzene

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:4333-76-0 SDS

4333-76-0Relevant academic research and scientific papers

Investigation of the Locked-Unlocked Mechanism in Living Anionic Polymerization Realized with 1-(Tri-isopropoxymethylsilylphenyl)-1-phenylethylene

Liu, Pibo,Ma, Hongwei,Han, Li,Shen, Heyu,Yang, Lincan,Li, Chao,Hao, Xinyu,Li, Yang

, p. 16538 - 16543 (2018)

Reported is an intriguing advance in living anionic polymerization (LAP) by a “locked-unlocked” mechanism in which the living anionic species can be quantitatively locked by end-capping with 1-(tri-isopropoxymethylsilylphenyl)-1-phenylethylene (DPE-Si(O-i

Photoredox-Catalyzed α-Aminomethyl Carboxylation of Styrenes with Sodium Glycinates: Synthesis of γ-Amino Acids and γ-Lactams

Zhou, Cong,Li, Miao,Sun, Jianwei,Cheng, Jiang,Sun, Song

supporting information, p. 2895 - 2899 (2021/05/05)

A visible-light photoredox-catalyzed reductive α-aminomethyl carboxylation of styrenes with sodium glycinates and CO2 has been developed to synthesize a series of α,α-disubstituted γ-amino acids and γ-lactams with high efficiency and regioselectivity. Notably, CO2 released from the decarboxylation step can be reused for the subsequent carboxylation. Distinct from the previous reactions with the same type of substrates leading to simple decarboxylation and olefin hydroalkylation, this process involves additional CO2 sequestration, thus leading to olefin α-aminomethyl carboxylation. These findings not only provide new access to α,α-disubstituted γ-amino acids and γ-lactams but also serve as a proof of concept for CO2 reutilization in decarboxylation reactions.

Visible-Light-Induced Meerwein Fluoroarylation of Styrenes

Tang, Hai-Jun,Zhang, Bin,Xue, Fei,Feng, Chao

supporting information, p. 4040 - 4044 (2021/05/26)

An unprecedented approach for assembling a broad range of 1,2-diarylethane derivatives with fluorine-containing fully substituted carbon centers was developed. The protocol features straightforward operation, proceeds under metal-free condition, and accommodates a large variety of synthetically useful functionalities. The critical aspect to the success of this novel transformation lies in using aryldiazonium salts as both aryl radical progenitor and also as single electron acceptor which elegantly enables a radical-polar crossover manifold.

Bimolecular vinylation of arenes by vinyl cations

Bour, Christophe,Gandon, Vincent,Li, Zhilong

supporting information, p. 6507 - 6510 (2020/07/02)

Styrene derivatives can be easily synthesized from vinyl triflates and arenes under mild reaction conditions, using [Li][Al(OC(CF3)3)4] as a catalyst and LiHMDS as a base. This transformation is likely to involve a vinyl cation intermediate as an electrophile, which is corroborated by DFT calculations, deuterium-labeling and other control experiments. The use of an inert weakly coordinating anion is a decisive factor in this bimolecular vinylation process. This journal is

Iodobenzene-catalyzed oxidative cleavage of olefins to carbonyl compounds

Du, Lele,Wang, Zechao,Wu, Junliang

, (2020/07/20)

A metal-free approach for the oxidative cleavage of carbon–carbon double bonds of olefins to carbonyl compounds was established by using oxidant m-CPBA and non-metallic organocatalyst PhI in toluene/H2O. A broad scope of aromatic olefins was used. All the reactions proceeded smoothly at 35 °C in short reaction time to furnish the respective mono- and double carbonyl compounds selectively in moderate to good yields.

Cu/Ni-Catalyzed Cyanomethylation of Alkenes with Acetonitrile for the Synthesis of β,γ-Unsaturated Nitriles

Jian, Hong,Shen, Zengming,Zhang, Saisai

, p. 6143 - 6150 (2020/05/22)

We have developed a protocol for the Cu/Ni-catalyzed cyanomethylation of alkenes with acetonitrile for the synthesis of β,γ-unsaturated nitriles. This is the first example of a direct coupling of the alkene sp2 C - H bond and the acetonitrile sp3 C - H bond for the preparation of β,γ-unsaturated nitriles. Acetonitrile, an inexpensive and stable solvent, is demonstrated to be a useful cyanomethyl source. The combination of copper and nickel catalysts resulted in a high reaction efficiency.

Bisoxazoline-pincer ligated cobalt-catalyzed hydrogenation of alkenes

Ritz, Mikhaila D.,Parsons, Astrid M.,Palermo, Philip N.,Jones, William D.

supporting information, (2020/02/13)

The efficient and atom economical hydrogenation of alkenes using a novel bisoxazoline ligated cobalt complex has been developed. The hydrogenation of a variety of alkenes containing electron neutral and electron-donating groups proceeds in high yield, whi

Synthesis of Trifluoromethylated Tetrasubstituted Allenes via Palladium-Catalyzed Carbene Transfer Reaction

Koenigs, Rene M.,Pei, Chao,Yang, Zhen

supporting information, p. 7300 - 7304 (2020/10/02)

Herein, we report on the palladium-catalyzed synthesis of trifluoromethylated, tetrasubstituted allenes from vinyl bromides and trifluoromethylated diazoalkanes in good to excellent yield. This reaction proceeds via oxidative addition of a Pd(0) complex w

Method for synthesizing alpha,beta-unsaturated selenium compound

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Paragraph 0062-0065, (2019/11/28)

The invention belongs to the field of organic selenium chemistry, and particularly relates to a method for synthesizing an alpha,beta-unsaturated selenium compound. The compound is synthesized by using an aryl boronic acid compound, elemental selenium and a diarylethene compound as reaction substrates. The method avoids toxic selenium-mercury reagents and toxic selenide reagents, conforms to the modern green development concept, and provides a green and economical method for synthesizing unsaturated selenium compounds in the future.

THERAPEUTIC COMPOUNDS

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Paragraph 00296, (2019/12/25)

The present disclosure relates to compounds of formula (I): and pharmaceutically acceptable salts thereof, wherein R1-R3 have any of the values defined herein, and compositions and uses thereof. The compounds are useful as inhibitors

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