2-Bromoethyl ether

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2-Bromoethyl ether
Bis(bromoethyl) ether.png
Names
Preferred IUPAC name
2-Bromo-1-(2-bromoethoxy)ethane
Other names
Bromex
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.024.095 Edit this at Wikidata
EC Number
  • 226-504-2
UNII
  • InChI=1S/C4H8Br2O/c5-1-3-7-4-2-6/h1-4H2
    Key: FOZVXADQAHVUSV-UHFFFAOYSA-N
  • C(CBr)OCCBr
Properties
Density 1.845
1.5140
Hazards
GHS labelling:
GHS05: CorrosiveGHS07: Exclamation mark
Danger
H315, H318, H335
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P310, P312, P321, P332+P313, P362, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

2-Bromoethyl ether (or Bis(2-bromoethyl) ether) is an organobromine compound that is also an ether. It is used in the manufacture of pharmaceuticals and crown ethers.[1][2][3]

References[edit]

  1. ^ Kudryatsev, K. V.; Samofin, V. V. (January 1997). "New approach to the synthesis of dibenzodithia-and benzothiaazacrown ethers via the aromatization of 2-alkylthio(arylthio)cyclohexanes during bromination". Chemistry of Heterocyclic Compounds. 33 (1): 106–111. doi:10.1007/BF02290756. S2CID 95541398.
  2. ^ Hansen, Thomas K.; Jørgensen, Tine; Becher, Jan (1992). "A sodium ion-sensitive tetrathiafulvalene: preparation and redox properties". J. Chem. Soc., Chem. Commun. (21): 1550–1552. doi:10.1039/C39920001550.
  3. ^ Akiyama, Masayasu; Katoh, Akira; Ogawa, Takuya (1989). "N-hydroxy amides. Part 8. Synthesis and iron(III)-holding properties of di- and tri-hydroxamic acids extending from benzene-di- and -tri-carbonyl units through oligo(ethyleneoxy) arms". Journal of the Chemical Society, Perkin Transactions 2 (9): 1213. doi:10.1039/P29890001213.