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Technology Process of 2,6-Dibromo-4-Isopropylphenyl Isocyanate

2,6-Dibromo-4-Isopropylphenyl Isocyanate

Base Information
  • Chemical Name:2,6-Dibromo-4-Isopropylphenyl Isocyanate
  • CAS No.:306935-84-2
  • Molecular Formula:C10H9 Br2 N O
  • Molecular Weight:318.99
  • Hs Code.:2929109000
  • DSSTox Substance ID:DTXSID10371036
  • Mol file:306935-84-2.mol
2,6-Dibromo-4-Isopropylphenyl Isocyanate

Synonyms:2,6-Dibromo-4-Isopropylphenyl Isocyanate;306935-84-2;1,3-dibromo-2-isocyanato-5-propan-2-ylbenzene;2,6-Dibromo-4-isopropylphenylisocyanate;1,3-dibromo-2-isocyanato-5-isopropylbenzene;SCHEMBL1020356;DTXSID10371036;FT-0610549;1,3-dibromo-2-isocyanato-5-isopropyl-benzene;A820532;1,3-Dibromo-2-isocyanato-5-(prop-2-yl)benzene, 1,3-Dibromo-2-isocyanato-5-isopropylbenzene

Suppliers and Price of 2,6-Dibromo-4-Isopropylphenyl Isocyanate
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
  • SynQuest Laboratories
  • 2,6-Dibromo-4-isopropylphenyl isocyanate
  • 100 mg
  • $ 16.00
  • Apolloscientific
  • 2,6-Dibromo-4-isopropylphenylisocyanate
  • 100mg
  • $ 15.00
  • AHH
  • 2,6-Dibromo-4-isopropylphenylisocyanate 97%
  • 50g
  • $ 400.00
Total 6 raw suppliers
Chemical Property of 2,6-Dibromo-4-Isopropylphenyl Isocyanate
Chemical Property:
  • Vapor Pressure:0.000107mmHg at 25°C 
  • Refractive Index:1.595 
  • Boiling Point:337.2°Cat760mmHg 
  • Flash Point:157.7°C 
  • PSA：29.43000 
  • Density:1.67g/cm3 
  • LogP:4.30230 
  • XLogP3:5.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:318.90304
  • Heavy Atom Count:14
  • Complexity:226
Purity/Quality:

97% *data from raw suppliers

2,6-Dibromo-4-isopropylphenyl isocyanate *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)C1=CC(=C(C(=C1)Br)N=C=O)Br
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