4-Bromo-2-chlorophenol

4-Bromo-2-chlorophenol
  • CAS No.:3964-56-5
Other grades of this product :
4-Bromo-2-chlorophenol Basic information
Product Name:4-Bromo-2-chlorophenol
Synonyms:4-BROMO-2-CHLOROPHENOL;AKOS BBB/367;4-Bromo-2-Chloro Phenol 2-Chloro-4-Bromo Phenol;4-Bromo-2-chlorophenol,98%;2-CHLORO-4-BROMO PHENOL;4-Bromo-2-chlorophenol,99%;4-BroMo-2-chlorophenol, 99% 25GR;4-Bromo-2-chL
CAS:3964-56-5
MF:C6H4BrClO
MW:207.45
EINECS:223-572-5
Product Categories:API Intermediate;Pyrazines;Aromatic Phenols;Phenol&Thiophenol&Mercaptan;Bromine Compounds;Chlorine Compounds;Phenols;Organic Building Blocks;Oxygen Compounds
Mol File:3964-56-5.mol
4-Bromo-2-chlorophenol Chemical Properties
Melting point 47-49 °C (lit.)
Boiling point 232-235 °C (lit.)
density 1.6170
refractive index 1.5859
Fp >230 °F
storage temp. Inert atmosphere,Room Temperature
Water Solubility Practically insoluble in water
form Low Melting Mass or Crystalline Needles, Powder and Chunks
pka7.92±0.18(Predicted)
color White to off-white
BRN 2042867
InChIKeyVIBJPUXLAKVICD-UHFFFAOYSA-N
CAS DataBase Reference3964-56-5(CAS DataBase Reference)
NIST Chemistry ReferencePhenol, 4-bromo-2-chloro-(3964-56-5)
EPA Substance Registry SystemPhenol, 4-bromo-2-chloro- (3964-56-5)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39-24/25
RIDADR UN 3077 9/PG 3
WGK Germany 3
HazardClass IRRITANT
HS Code 29081990
MSDS Information
ProviderLanguage
4-Bromo-2-chlorophenol English
ACROS English
SigmaAldrich English
ALFA English
4-Bromo-2-chlorophenol Usage And Synthesis
Chemical Propertieswhite to off-white low melting mass or crystalline
Uses4-Bromo-2-chlorophenol was used as reagent during the synthesis of 7-arylbenzo[b][1,4]oxazin derivatives.
DefinitionChEBI: A halophenol that is phenol in which the hydrogens at positions 2 and 4 have been replaced by chlorine and bromine, respectively.
General Description4-Bromo-2-chlorophenol is biologically inactive metabolite of profenofos, an organophosphorus pesticide. It undergoes enzyme-catalyzed copolymerization with phenols catalyzed by extracellular laccase of the fungus Rhizoctonia praticola.

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