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N-(4-acetylphenyl)-2-bromoacetamide

Base Information Edit
  • Chemical Name:N-(4-acetylphenyl)-2-bromoacetamide
  • CAS No.:29182-93-2
  • Molecular Formula:C10H10BrNO2
  • Molecular Weight:256.099
  • Hs Code.:
  • DSSTox Substance ID:DTXSID701292168
  • Mol file:29182-93-2.mol
N-(4-acetylphenyl)-2-bromoacetamide

Synonyms:N-(4-acetylphenyl)-2-bromoacetamide;29182-93-2;SCHEMBL7687241;DTXSID701292168;MFCD02974382;STL570931;AKOS005172611;LS-03580

Suppliers and Price of N-(4-acetylphenyl)-2-bromoacetamide
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
  • Matrix Scientific
  • N-(4-Acetylphenyl)-2-bromoacetamide
  • 1g
  • $ 258.00
  • Crysdot
  • N-(4-Acetylphenyl)-2-bromoacetamide 97%
  • 5g
  • $ 527.00
  • Biosynth Carbosynth
  • N-(4-Acetylphenyl)-2-bromoacetamide
  • 5 g
  • $ 578.00
  • Biosynth Carbosynth
  • N-(4-Acetylphenyl)-2-bromoacetamide
  • 2 g
  • $ 289.00
  • Biosynth Carbosynth
  • N-(4-Acetylphenyl)-2-bromoacetamide
  • 1 g
  • $ 170.00
  • Biosynth Carbosynth
  • N-(4-Acetylphenyl)-2-bromoacetamide
  • 500 mg
  • $ 100.00
  • Biosynth Carbosynth
  • N-(4-Acetylphenyl)-2-bromoacetamide
  • 250 mg
  • $ 57.50
  • AK Scientific
  • N-(4-Acetylphenyl)-2-bromoacetamide
  • 500mg
  • $ 185.00
Total 2 raw suppliers
Chemical Property of N-(4-acetylphenyl)-2-bromoacetamide Edit
Chemical Property:
  • XLogP3:2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:3
  • Exact Mass:254.98949
  • Heavy Atom Count:14
  • Complexity:222
Purity/Quality:

98%min *data from raw suppliers

N-(4-Acetylphenyl)-2-bromoacetamide *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(=O)C1=CC=C(C=C1)NC(=O)CBr
Technology Process of N-(4-acetylphenyl)-2-bromoacetamide

There total 4 articles about N-(4-acetylphenyl)-2-bromoacetamide 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 potassium carbonate; In dichloromethane; water; at 0 - 20 ℃;
DOI:10.1016/j.ejmech.2013.11.006
Guidance literature:
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 0 - 20 ℃;
DOI:10.1021/jm070564e
Guidance literature:
Multi-step reaction with 2 steps
1: zinc chloride / Verseifen des Reaktionsprodukts mit Salzsaeure
2: sodium acetate; aqueous acetic acid
With sodium acetate; acetic acid; zinc(II) chloride;
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