1-(2-Bromoethenyl)-3-methylbenzene

Base Information

Chemical Name:1-(2-Bromoethenyl)-3-methylbenzene
CAS No.:115665-69-5
Molecular Formula:C₉H₉Br
Molecular Weight:197.074
Hs Code.:
DSSTox Substance ID:DTXSID201281390
Nikkaji Number:J1.545.979D

Synonyms:1-(2-bromoethenyl)-3-methylbenzene;115665-69-5;SCHEMBL11867135;(E)-beta-Bromo-3-methylstyrene;DTXSID201281390;1-(2-Bromovinyl)-3-methylbenzene;1-[(1E)-2-Bromoethenyl]-3-methylbenzene;CS-0280876;EN300-125202

Suppliers and Price of 1-(2-Bromoethenyl)-3-methylbenzene

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 2 raw suppliers

Chemical Property of 1-(2-Bromoethenyl)-3-methylbenzene

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:1
Exact Mass:195.98876
Heavy Atom Count:10
Complexity:118

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC(=CC=C1)C=CBr
Isomeric SMILES:CC1=CC(=CC=C1)/C=C/Br

Technology Process of 1-(2-Bromoethenyl)-3-methylbenzene

There total 16 articles about 1-(2-Bromoethenyl)-3-methylbenzene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 71.0%

: 766-82-5
1-ethynyl-3-methyl-benzene

: 115665-69-5,115665-62-8
1-[(E)-2-bromoethenyl]-3-methylbenzene

Guidance literature:: With chloro[1,3-bis(2,6-di-i-propylphenyl)imidazol-2-ylidene]copper(I); 1,2-dibromo-1,1,2,2-tetrachloroethane; diphenylsilane; 2-tert-butylphenol potassium salt; In toluene; at 25 ℃; for 0.5h; stereoselective reaction; Glovebox; Inert atmosphere; Schlenk technique;
DOI:10.1021/ja503944n

Reference yield:

: 3029-79-6,14473-89-3,16642-82-3
(E)-3-methylcinnamic acid

: 115665-69-5,115665-62-8
(Z)-1-(2-bromovinyl)-3-methylbenzene

: 115665-69-5,115665-62-8
1-[(E)-2-bromoethenyl]-3-methylbenzene

Guidance literature:: With sodium hydrogencarbonate; 1-n-butyl-3-methylimidazolim bromide; 1-butyl-3-methylimidazolium tribromide; at 40 - 50 ℃; for 2h;

Reference yield:

: 3029-79-6,14473-89-3,16642-82-3
(E)-3-methylcinnamic acid

: 115665-69-5,115665-62-8
(Z)-1-(2-bromovinyl)-3-methylbenzene

: 115665-69-5,115665-62-8
1-[(E)-2-bromoethenyl]-3-methylbenzene

Guidance literature:: With sodium hydrogencarbonate; 1-n-butyl-3-methylimidazolim bromide; 1-butyl-3-methylimidazolium tribromide; at 40 - 50 ℃; for 2h;

upstream raw materials:

1-(2,2-dibromovinyl)-3-methylbenzene

(E)-3-methylcinnamic acid

m-tolyl aldehyde

3-methylcinnamic acid

Downstream raw materials:

(Z)-1-(3-methylstyryl)-1H-imidazole

(Z)-1-(3-methylstyryl)-1H-benzo[d]imidazole

N-(4-methylphenyl)-3-exo-(3-methylbenzylidene)tricyclo[3.2.1.02,4]octane-6,7-endo-dicarboximide

N-isobutyl-3-exo-(3-methylbenzylidene)tricyclo[3.2.1.02,4]octane-6,7-endo-dicarboximide

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