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Ethyl 2-(bromomethyl)-3-fluorobenzoate

Base Information Edit
  • Chemical Name:Ethyl 2-(bromomethyl)-3-fluorobenzoate
  • CAS No.:114312-58-2
  • Molecular Formula:C10H10BrFO2
  • Molecular Weight:261.091
  • Hs Code.:
  • DSSTox Substance ID:DTXSID401283566
  • Mol file:114312-58-2.mol
Ethyl 2-(bromomethyl)-3-fluorobenzoate

Synonyms:Ethyl 2-(bromomethyl)-3-fluorobenzoate;114312-58-2;SCHEMBL5250458;HCTSRCSPFWZIGA-UHFFFAOYSA-N;DTXSID401283566;ethyl 3-fluoro-2-bromomethylbenzoate;Ethyl2-(bromomethyl)-3-fluorobenzoate

Suppliers and Price of Ethyl 2-(bromomethyl)-3-fluorobenzoate
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Ethyl 2-(bromomethyl)-3-fluorobenzoate Edit
Chemical Property:
  • Vapor Pressure:0.000432mmHg at 25°C 
  • XLogP3:2.8
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:4
  • Exact Mass:259.98482
  • Heavy Atom Count:14
  • Complexity:199
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCOC(=O)C1=C(C(=CC=C1)F)CBr
Technology Process of Ethyl 2-(bromomethyl)-3-fluorobenzoate

There total 2 articles about Ethyl 2-(bromomethyl)-3-fluorobenzoate 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:
With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; at 80 ℃;
Guidance literature:
Multi-step reaction with 2 steps
1: thionyl chloride / 20 h / 0 - 80 °C
2: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / 17 h / 82 °C / Inert atmosphere
With N-Bromosuccinimide; thionyl chloride; dibenzoyl peroxide; In tetrachloromethane;
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