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Technology Process of N-(3-acetylphenyl)-2-(4-chlorophenyl)acetamide

N-(3-acetylphenyl)-2-(4-chlorophenyl)acetamide

Base Information
  • Chemical Name:N-(3-acetylphenyl)-2-(4-chlorophenyl)acetamide
  • CAS No.:72116-70-2
  • Molecular Formula:C16H14ClNO2
  • Molecular Weight:287.74
  • Hs Code.:
  • DSSTox Substance ID:DTXSID601261564
  • Mol file:72116-70-2.mol
N-(3-acetylphenyl)-2-(4-chlorophenyl)acetamide

Synonyms:N-(3-acetylphenyl)-2-(4-chlorophenyl)acetamide;72116-70-2;Cambridge id 6245426;DTXSID601261564;BBL015282;MFCD01353447;STK255773;AKOS000167084;VS-04883;CS-0314586;N-(3-Acetylphenyl)-4-chlorobenzeneacetamide;Z30816350

Suppliers and Price of N-(3-acetylphenyl)-2-(4-chlorophenyl)acetamide
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
  • Matrix Scientific
  • N-(3-Acetylphenyl)-2-(4-chlorophenyl)acetamide
  • 500mg
  • $ 95.00
  • Crysdot
  • N-(3-Acetylphenyl)-2-(4-chlorophenyl)acetamide 97%
  • 5g
  • $ 407.00
  • American Custom Chemicals Corporation
  • N-(3-ACETYLPHENYL)-2-(4-CHLOROPHENYL)ACETAMIDE 95.00%
  • 5G
  • $ 1155.00
  • American Custom Chemicals Corporation
  • N-(3-ACETYLPHENYL)-2-(4-CHLOROPHENYL)ACETAMIDE 95.00%
  • 1G
  • $ 693.00
  • American Custom Chemicals Corporation
  • N-(3-ACETYLPHENYL)-2-(4-CHLOROPHENYL)ACETAMIDE 95.00%
  • 0.5G
  • $ 638.00
Total 2 raw suppliers
Chemical Property of N-(3-acetylphenyl)-2-(4-chlorophenyl)acetamide
Chemical Property:
  • PKA:13.89±0.70(Predicted) 
  • XLogP3:3.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:4
  • Exact Mass:287.0713064
  • Heavy Atom Count:20
  • Complexity:350
Purity/Quality:

98%min *data from raw suppliers

N-(3-Acetylphenyl)-2-(4-chlorophenyl)acetamide *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:Xi 
MSDS Files:
Useful:
  • Canonical SMILES:CC(=O)C1=CC(=CC=C1)NC(=O)CC2=CC=C(C=C2)Cl
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