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1-Bromo-3-iodobenzene

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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
  • 591-18-4
Mol File:
591-18-4.mol
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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.)
Flash point:
>230 °F
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Chloroform (Sparingly), Ethyl Acetate (Slightly)
form 
Oil
color 
Colourless
Specific Gravity
2.219
Water Solubility 
insoluble
Sensitive 
Light Sensitive
BRN 
1854384
InChIKey
CTPUUDQIXKUAMO-UHFFFAOYSA-N
CAS DataBase Reference
591-18-4(CAS DataBase Reference)
NIST Chemistry Reference
3-Bromoiodobenzene(591-18-4)
EPA Substance Registry System
Benzene, 1-bromo-3-iodo- (591-18-4)
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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

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1-Bromo-3-iodobenzene Usage And Synthesis

Chemical Properties

Clear colourless to light yellow liquid

Chemical Properties

Light sensitive. Incompatible with strong oxidizing agents, strong bases and strong acids. Store in a cool place.

Uses

1-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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