1-bromopropene

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Structural formula
Structural formula of 1-bromopropene
General
Surname 1-bromopropene
other names
  • 1-propenyl bromide
  • 1-bromo-1-propene
Molecular formula C 3 H 5 Br
Brief description

colorless liquid

External identifiers / databases
CAS number
  • 590-14-7
  • 590-13-6 ( cis )
  • 590-15-8 ( trans )
PubChem 11533
Wikidata Q55997769
properties
Molar mass 120.98 g mol −1
Physical state

liquid

density
  • 1.423 g cm −3 (25 ° C)
  • 1.408 g cm −3 (25 ° C) ( trans )
Melting point

−113 ° C ( cis )

boiling point
  • 58 ° C
  • 64-65 ° C ( trans )
solubility
  • practically insoluble in water
  • soluble in ether, acetone and chloroform
safety instructions
GHS labeling of hazardous substances
02 - Highly / extremely flammable 07 - Warning

danger

H and P phrases H: 225-315-319-335
P: 210-261-305 + 351 + 338
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

1-bromopropene is a chemical compound from the group of haloalkenes.

Extraction and presentation

1-bromopropene can be obtained by dehydrohalogenation of 1,2-dibromopropane .

properties

1-bromopropene is a colorless liquid that is practically insoluble in water.

use

1-bromopropene can be used to synthesize other chemical compounds.

Individual evidence

  1. ↑ a b c d e f g Data sheet 1-Bromo-1-propene (cis and trans), 98% from Sigma-Aldrich , accessed on August 6, 2018 ( PDF ).
  2. ↑ a b Data sheet trans-1-Bromo-1-propene, contains copper as stabilizer, 99% from Sigma-Aldrich , accessed on August 6, 2018 ( PDF ).
  3. ↑ a b c d David R. Lide: CRC Handbook of Chemistry and Physics A Ready-reference Book of Chemical and Physical Data . CRC Press, 1995, ISBN 978-0-8493-0595-5 , pp. 74 ( limited preview in Google Book search).
  4. ↑ Data sheet cis-1-Bromo-1-propene, 97% from Sigma-Aldrich , accessed on August 6, 2018 ( PDF ).
  5. ↑ SK Bhasin, Reena Gupta: Pharmaceutical Organic Chemistry E-Book . Elsevier Health Sciences, 2013, ISBN 978-81-312-3267-5 , pp. 262 ( limited preview in Google Book search).
  6. ↑ Julien Beignet, Sherry R. Chemler, Steven J. Collier, Gwilherm Evano, Robert Garbaccio: Science of Synthesis: Houben-Weyl Methods of Molecular Transformations Vol. 20b Three Carbon-Heteroatom Bonds: Esters, and Lactones; Peroxy Acids and R (CO) OX Compounds; R (CO) X, X = S, Se, Te . Georg Thieme Verlag, 2014, ISBN 3-13-171941-9 , p. 1261 ( limited preview in Google Book search).