1-Bromo-3-iodobenzene

1-Bromo-3-iodobenzene
  • CAS No.:591-18-4
Other grades of this product :
1-Bromo-3-iodobenzene Basic information
Product Name:1-Bromo-3-iodobenzene
Synonyms:Benzene, 1-bromo-3-iodo-;m-Bromoiodobenzene;1-BROMO-3-IODOBENZENE;3-BROMOIODOBENZENE;3-Bromoiodobenzene m-Bromoiodobenzene;1-Bromo-3-iodobenzene,98%;3-bromoiodbenzene;3-BROMO-1-IODOBENZENE
CAS:591-18-4
MF:C6H4BrI
MW:282.9
EINECS:209-703-9
Product Categories:Organohalides;Aromatic Hydrocarbons (substituted) & Derivatives;API intermediates;Miscellaneous;Bromine Compounds;Iodine Compounds;Aryl;C6;Halogenated Hydrocarbons;bc0001
Mol File:591-18-4.mol
1-Bromo-3-iodobenzene Chemical Properties
Melting point −9.3-−9 °C(lit.)
Boiling point 120 °C18 mm Hg(lit.)
density 2.219 g/mL at 25 °C(lit.)
refractive index n20/D 1.66(lit.)
Fp >230 °F
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Chloroform (Sparingly), Ethyl Acetate (Slightly)
form Oil
color Colourless
Specific Gravity2.219
Water Solubility insoluble
Sensitive Light Sensitive
BRN 1854384
InChIKeyCTPUUDQIXKUAMO-UHFFFAOYSA-N
CAS DataBase Reference591-18-4(CAS DataBase Reference)
NIST Chemistry Reference3-Bromoiodobenzene(591-18-4)
EPA Substance Registry SystemBenzene, 1-bromo-3-iodo- (591-18-4)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39-24/25
WGK Germany 3
Hazard Note Irritant
TSCA T
HazardClass IRRITANT, LIGHT SENSITIVE
HS Code 29039990
MSDS Information
ProviderLanguage
1-Bromo-3-iodobenzene English
SigmaAldrich English
ACROS English
ALFA English
1-Bromo-3-iodobenzene Usage And Synthesis
Chemical PropertiesClear colourless to light yellow liquid
Chemical PropertiesLight sensitive. Incompatible with strong oxidizing agents, strong bases and strong acids. Store in a cool place.
Uses1-Bromo-3-iodobenzene is used in the preparation of 3'-bromo-2,3,4,5,6-pentaethyl-biphenyl by reacting with hex-3-yne. It is also used to prepare 1-(3'-bromophenyl)-3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodec-1-ene and 1-(3'-bromophenyl)-3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooct-1-ene. Further, it is involved in the preparation of oxygen-tethered 1,6-enynes.

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