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Technology Process of N-(4-Bromo-2-isopropylphenyl)-2-(4-ethylphenoxy)acetamide

N-(4-Bromo-2-isopropylphenyl)-2-(4-ethylphenoxy)acetamide

Base Information
  • Chemical Name:N-(4-Bromo-2-isopropylphenyl)-2-(4-ethylphenoxy)acetamide
  • CAS No.:528531-90-0
  • Molecular Formula:C19H22BrNO2
  • Molecular Weight:376.29
  • Hs Code.:2924299090
  • DSSTox Substance ID:DTXSID40361748
  • Wikidata:Q82144232
N-(4-Bromo-2-isopropylphenyl)-2-(4-ethylphenoxy)acetamide

Synonyms:528531-90-0;N-(4-BROMO-2-ISOPROPYLPHENYL)-2-(4-ETHYLPHENOXY)ACETAMIDE;CHEMBRDG-BB 7087119;N-[4-bromo-2-(propan-2-yl)phenyl]-2-(4-ethylphenoxy)acetamide;N-(4-bromo-2-propan-2-ylphenyl)-2-(4-ethylphenoxy)acetamide;DTXSID40361748;MFCD03555609;STK124626;AKOS000368216;BS-38066

Suppliers and Price of N-(4-Bromo-2-isopropylphenyl)-2-(4-ethylphenoxy)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
  • ChemBridge Corporation
  • N-(4-bromo-2-isopropylphenyl)-2-(4-ethylphenoxy)acetamide 95%
  • 1 g
  • $ 23.00
  • American Custom Chemicals Corporation
  • N-(4-BROMO-2-ISOPROPYLPHENYL)-2-(4-ETHYLPHENOXY)ACETAMIDE 95.00%
  • 5MG
  • $ 497.26
Total 1 raw suppliers
Chemical Property of N-(4-Bromo-2-isopropylphenyl)-2-(4-ethylphenoxy)acetamide
Chemical Property:
  • Vapor Pressure:9.13E-11mmHg at 25°C 
  • Boiling Point:516.3°C at 760 mmHg 
  • Flash Point:266°C 
  • PSA：38.33000 
  • Density:1.297g/cm3 
  • LogP:5.22540 
  • XLogP3:5.4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:6
  • Exact Mass:375.08339
  • Heavy Atom Count:23
  • Complexity:366
Purity/Quality:

99% *data from raw suppliers

N-(4-bromo-2-isopropylphenyl)-2-(4-ethylphenoxy)acetamide 95% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCC1=CC=C(C=C1)OCC(=O)NC2=C(C=C(C=C2)Br)C(C)C
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