1,3-Dibromobenzene

1,3-Dibromobenzene
  • CAS No.:108-36-1
Other grades of this product :
1,3-Dibromobenzene Basic information
Product Name:1,3-Dibromobenzene
Synonyms:1,3-dibromo-benzen;Benzene, m-dibromo-;Benzene,1,3-dibromo-;m-dibromo-benzen;1,3-DIBROMOBENZENE;META-DIBROMOBENZENE;M-DIBROMOBENZENE;1,3-Dibromobenzene97%
CAS:108-36-1
MF:C6H4Br2
MW:235.9
EINECS:203-574-2
Product Categories:alkyl bromide;Bromine Compounds;Benzene derivates;Aryl;C6;Halogenated Hydrocarbons
Mol File:108-36-1.mol
1,3-Dibromobenzene Chemical Properties
Melting point -7 °C (lit.)
Boiling point 218-219 °C (lit.)
density 1.952 g/mL at 25 °C (lit.)
vapor density 8.16 (vs air)
vapor pressure 5 mm Hg ( 66 °C)
refractive index n20/D 1.608(lit.)
Fp 201 °F
storage temp. Sealed in dry,Room Temperature
solubility 0.068g/l
form Liquid
Specific Gravity1.952
color Clear colorless to light yellow
Water Solubility insoluble
BRN 1904538
CAS DataBase Reference108-36-1(CAS DataBase Reference)
NIST Chemistry ReferenceBenzene, 1,3-dibromo-(108-36-1)
EPA Substance Registry Systemm-Dibromobenzene (108-36-1)
Safety Information
Hazard Codes Xi,C
Risk Statements 36/37/38
Safety Statements 26-36-24/25
RIDADR UN 2711
WGK Germany 2
RTECS CZ1790000
Hazard Note Irritant
TSCA T
HazardClass 3.2
PackingGroup III
HS Code 29036990
MSDS Information
ProviderLanguage
1,3-Dibromobenzene English
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1,3-Dibromobenzene Usage And Synthesis
Chemical Propertiesclear colourless to light yellow liquid
Uses1,3-Dibromobenzene is used in Suzuki coupling reaction for the preparation of [n]metacyclophanes. It is used to prepare 5-(3-bromo-phenyl)-2,4-di-tert-butoxy-pyrimidine using Pd(0) (PPh3)4 as a reagent. Further, it undergoes solid-supported potassium fluoride-aluminum oxide palladium-catalyzed polyarylation reaction with phenyl boronic acid to get conjugated polyaryls.
DefinitionChEBI: A dibromobenzene carrying bromo groups at positions 1 and 3.
General Description1,3-Dibromobenzene undergoes solid-supported [KF-Al2O3] palladium-catalyzed polyarylation reaction with phenyl boronic acid under microwave irradiation to yield conjugated polyaryls.

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