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1-[5-(Benzyloxy)-2-bromophenyl]ethan-1-one

Base Information Edit
  • Chemical Name:1-[5-(Benzyloxy)-2-bromophenyl]ethan-1-one
  • CAS No.:105805-16-1
  • Molecular Formula:C15H13BrO2
  • Molecular Weight:305.171
  • Hs Code.:
  • DSSTox Substance ID:DTXSID30556823
  • Wikidata:Q82438522
  • Mol file:105805-16-1.mol
1-[5-(Benzyloxy)-2-bromophenyl]ethan-1-one

Synonyms:105805-16-1;1-[5-(Benzyloxy)-2-bromophenyl]ethan-1-one;SCHEMBL5801964;DTXSID30556823;1-(5-(Benzyloxy)-2-bromophenyl)ethanone

Suppliers and Price of 1-[5-(Benzyloxy)-2-bromophenyl]ethan-1-one
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
Total 1 raw suppliers
Chemical Property of 1-[5-(Benzyloxy)-2-bromophenyl]ethan-1-one Edit
Chemical Property:
  • XLogP3:3.8
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:4
  • Exact Mass:304.00989
  • Heavy Atom Count:18
  • Complexity:274
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(=O)C1=C(C=CC(=C1)OCC2=CC=CC=C2)Br
Technology Process of 1-[5-(Benzyloxy)-2-bromophenyl]ethan-1-one

There total 5 articles about 1-[5-(Benzyloxy)-2-bromophenyl]ethan-1-one 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 silica gel; pyridinium chlorochromate; In dichloromethane; at 20 ℃; for 2h; Inert atmosphere;
DOI:10.1021/ol2032625
Guidance literature:
With bromine; sodium acetate; In acetic acid; for 24h; Ambient temperature; in the dark;
Guidance literature:
Multi-step reaction with 2 steps
1.1: iodine; magnesium / diethyl ether / Inert atmosphere
1.2: 3 h / -10 °C / Inert atmosphere
1.3: Inert atmosphere
2.1: silica gel; pyridinium chlorochromate / dichloromethane / 2 h / 20 °C / Inert atmosphere
With iodine; silica gel; magnesium; pyridinium chlorochromate; In diethyl ether; dichloromethane; 1.2: Grignard reaction;
DOI:10.1021/ol2032625
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