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N-(5-Bromo-2-fluorobenzyl)phthalimide

Base Information Edit
  • Chemical Name:N-(5-Bromo-2-fluorobenzyl)phthalimide
  • CAS No.:530141-44-7
  • Molecular Formula:C15H9BrFNO2
  • Molecular Weight:334.144
  • Hs Code.:2925190090
  • European Community (EC) Number:610-936-7
  • DSSTox Substance ID:DTXSID80378411
  • Wikidata:Q82167919
  • Mol file:530141-44-7.mol
N-(5-Bromo-2-fluorobenzyl)phthalimide

Synonyms:530141-44-7;N-(5-Bromo-2-fluorobenzyl)phthalimide;2-(5-Bromo-2-fluorobenzyl)isoindoline-1,3-dione;2-[(5-bromo-2-fluorophenyl)methyl]isoindole-1,3-dione;2-[(5-bromo-2-fluorophenyl)methyl]-2,3-dihydro-1H-isoindole-1,3-dione;SCHEMBL17979154;DTXSID80378411;BNQNVOUVZHMFCA-UHFFFAOYSA-N;3-Chloropropionic acidphenyl ester;AKOS008652266;A829353;A1-37536;2-[(5-Bromo-2-fluorophenyl)methyl]-1H-isoindole-1,3(2H)-dione

Suppliers and Price of N-(5-Bromo-2-fluorobenzyl)phthalimide
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
  • American Custom Chemicals Corporation
  • N-(5-BROMO-2-FLUOROBENZYL)PHTHALIMIDE 95.00%
  • 5MG
  • $ 499.38
Total 7 raw suppliers
Chemical Property of N-(5-Bromo-2-fluorobenzyl)phthalimide Edit
Chemical Property:
  • Vapor Pressure:5.62E-08mmHg at 25°C 
  • Refractive Index:1.662 
  • Boiling Point:441 °C at 760 mmHg 
  • Flash Point:220.5 °C 
  • PSA:37.38000 
  • Density:1.66 g/cm3 
  • LogP:3.32230 
  • XLogP3:3.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:2
  • Exact Mass:332.98007
  • Heavy Atom Count:20
  • Complexity:393
Purity/Quality:

99% *data from raw suppliers

N-(5-BROMO-2-FLUOROBENZYL)PHTHALIMIDE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36/37/39 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C(=O)N(C2=O)CC3=C(C=CC(=C3)Br)F
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