2-Bromoethyl ether

2-Bromoethyl ether
Names
	Preferred IUPAC name 2-Bromo-1-(2-bromoethoxy)ethane
	Other names Bromex
Identifiers
CAS Number	5414-19-7 ;
3D model (JSmol)	Interactive image;
ChemSpider	20226;
ECHA InfoCard	100.024.095
EC Number	226-504-2;
PubChem CID	21521;
UNII	XTS6KN2SLA ;
CompTox Dashboard (EPA)	DTXSID1063851 ;
	InChI InChI=1S/C4H8Br2O/c5-1-3-7-4-2-6/h1-4H2 Key: FOZVXADQAHVUSV-UHFFFAOYSA-N;
	SMILES C(CBr)OCCBr;
Properties
Density	1.845
Refractive index (nD)	1.5140
Hazards
	GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H315, H318, H335
Precautionary statements	P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P310, P312, P321, P332+P313, P362, P403+P233, P405, P501
Related compounds
Related compounds	Bis(chloroethyl) ether
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

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]

^ 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.
^ 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.
^ 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.