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1,2-Dibromopropane

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1,2-Dibromopropane
Skeletal formula of 1,2-dibromopropane with some implicit hydrogens shown
Dibromopropane molecule
Names
Preferred IUPAC name 1,2-Dibromopropane
Other names Propylene dibromide
Identifiers
CAS Number
3D model (JSmol)
Beilstein Reference 1718884
ChemSpider
ECHA InfoCard 100.001.036 Edit this at Wikidata
EC Number
  • 201-139-1
MeSH 1,2-dibromopropane
PubChem CID
RTECS number
  • TX8574000
UNII
UN number 1993
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C3H6Br2/c1-3(5)2-4/h3H,2H2,1H3Key: XFNJYAKDBJUJAJ-UHFFFAOYSA-N
SMILES
  • CC(Br)CBr
Properties
Chemical formula C3H6Br2
Molar mass 201.889 g·mol
Appearance Colourless liquid
Density 1.937 g mL
Melting point −55.5 °C; −67.8 °F; 217.7 K
Boiling point 139 to 143 °C; 282 to 289 °F; 412 to 416 K
Henry's law
constant (kH) 		6.7 μmol Pa kg
Refractive index (nD) 1.519
Thermochemistry
Heat capacity (C) 172.8 J K mol
Hazards
GHS labelling:
Pictograms GHS02: Flammable GHS07: Exclamation mark
Signal word Warning
Hazard statements H226, H302, H332
Flash point 50 °C (122 °F; 323 K)
Lethal dose or concentration (LD, LC):
LD50 (median dose) 741 mg kg (oral, rat)
Related compounds
Related alkanes
Related compounds Mitobronitol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒N verify (what is  ?) Infobox references
Chemical compound

1,2-Dibromopropane, also known as propylene dibromide, is an organic compound with the formula CH3CHBrCH2Br. It is the simplest chiral hydrocarbon containing two bromine atoms:

(S)-1,2-Dibrompropane (above) and (R)-1,2-Dibrompropane (below)

References

1,2-Dibromo Propane also known as Propylene bromide is a naturally occurring organic compound. It is part of the Vicinal Dihalide family; it is highly unstable due to both torsional strain and its highly electrophilic nature.

  1. "PubChem". pubchem.ncbi.nlm.nih.gov.
  2. "1,2-dibromopropane - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 27 March 2005. Identification. Retrieved 21 June 2012.


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