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Ethyl 4-bromomethylcinnamate

Base Information Edit
  • Chemical Name:Ethyl 4-bromomethylcinnamate
  • CAS No.:60682-98-6
  • Molecular Formula:C12H13BrO2
  • Molecular Weight:269.138
  • Hs Code.:2916399090
  • Mol file:60682-98-6.mol
Ethyl 4-bromomethylcinnamate

Synonyms:4-Bromomethylcinnamicacid ethyl ester;Ethyl p-(bromomethyl)cinnamate;Ethyl 4-bromomethylcinnamate;

Suppliers and Price of Ethyl 4-bromomethylcinnamate
Supply Marketing:Edit
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
  • Usbiological
  • Ethyl 4-Bromomethylcinnamate
  • 2.5mg
  • $ 425.00
  • TRC
  • Ethyl4-Bromomethylcinnamate
  • 2.5mg
  • $ 130.00
  • TRC
  • Ethyl4-Bromomethylcinnamate
  • 25mg
  • $ 1050.00
  • American Custom Chemicals Corporation
  • 2-PROPENOIC ACID, 3-[4-(BROMOMETHYL)-PHENYL]-ETHYL ESTER 95.00%
  • 25MG
  • $ 1732.50
  • American Custom Chemicals Corporation
  • 2-PROPENOIC ACID, 3-[4-(BROMOMETHYL)-PHENYL]-ETHYL ESTER 95.00%
  • 2.5MG
  • $ 687.50
Total 37 raw suppliers
Chemical Property of Ethyl 4-bromomethylcinnamate Edit
Chemical Property:
  • Vapor Pressure:5.27E-05mmHg at 25°C 
  • Refractive Index:1.585 
  • Boiling Point:347.8 °C at 760 mmHg 
  • Flash Point:164.1 °C 
  • PSA:26.30000 
  • Density:1.37 g/cm3 
  • LogP:3.15780 
Purity/Quality:

98%,99%, *data from raw suppliers

Ethyl 4-Bromomethylcinnamate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses Ethyl 4-bromomethylcinnamate can be used in the preparation of cinnamamide derivative as 5α-reductase inhibitors. Used in the preparation of cinnamamide derivative as 5α-reductase inhibitors.
Technology Process of Ethyl 4-bromomethylcinnamate

There total 2 articles about Ethyl 4-bromomethylcinnamate 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:
Guidance literature:
ethyl p-methylcinnamate; In tetrachloromethane; at 110 ℃; for 1h; under 3040.2 Torr; Inert atmosphere;
With dodecyltrimethylammonium bromide; acetic acid; In tetrachloromethane; at 140 ℃; for 5h; under 5320.36 Torr;
Guidance literature:
Entspr. Toluol, NBS;
Guidance literature:
Multi-step reaction with 3 steps
1: xylene / 24 h / Heating
2: sodium ethoxide / ethanol
3: ethanol / 168 h / Ambient temperature
With sodium ethanolate; In ethanol; xylene;
Refernces Edit
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