2-Phenoxyethylbromide

2-Phenoxyethylbromide
  • CAS No.:589-10-6
Other grades of this product :
2-Phenoxyethylbromide Basic information
Product Name:2-Phenoxyethylbromide
Synonyms:(2-bromoethoxy)-benzen;Benzene,(2-bromoethoxy)-;-Bromophenetole;Phenetole, beta-bromo-;PHENOXYETHYLBROMIDE;(2-BROMOETHOXY)BENZENE;2-BROMOETHYL PHENYL ETHER;(2-BROMETHOXY)BENZENE
CAS:589-10-6
MF:C8H9BrO
MW:201.06
EINECS:209-634-4
Product Categories:Aromatic Ethers;Phenetole;Aromatics Compounds;Anisoles, Alkyloxy Compounds & Phenylacetates;Bromine Compounds;Aromatics;Pharmaceutical Intermediates
Mol File:589-10-6.mol
2-Phenoxyethylbromide Chemical Properties
Melting point 31-34 °C(lit.)
Boiling point 144 °C40 mm Hg(lit.)
density 1.45
refractive index 1.555-1.557
Fp 150 °F
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Solubility in methanol is almost transparent. Soluble in chloroform and ethyl acetate.
form Liquid After Melting
color Clear colorless
Water Solubility Insoluble in water.
BRN 508290
CAS DataBase Reference589-10-6(CAS DataBase Reference)
NIST Chemistry ReferenceBenzene, (2-bromoethoxy)-(589-10-6)
EPA Substance Registry SystemBenzene, (2-bromoethoxy)- (589-10-6)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-22
Safety Statements 23-24/25-26
RIDADR 1325
WGK Germany 3
Hazard Note Irritant
TSCA Yes
HazardClass 4.1
PackingGroup II
HS Code 29093038
MSDS Information
ProviderLanguage
beta-Bromophenetole English
SigmaAldrich English
ACROS English
ALFA English
2-Phenoxyethylbromide Usage And Synthesis
Chemical PropertiesWhite Solid
Uses2-Phenoxyethyl bromide is used in the synthesis and antihypertensive activity of 4'-substituted spiro[4H-3,1-benzoxazine-4,4'-piperidin]-2(1H)-ones.
Application2-Phenoxyethyl bromide can be used as a pharmaceutical intermediate for the synthesis of nafazodone and oxiperomide.
Preparation2-Phenoxyethyl bromide is synthesized by the reaction of phenol and dibromoethane. Put phenol, dibromoethane and sodium hydroxide in a reaction pot and stir and mix, react at 110 °C for 6 hours, recover dibromoethane, the recovery amount is about 60%, wash with 5% sodium hydroxide solution and water, and divide Take the oil layer, distill under reduced pressure, and collect the fractions at 130-150°C (6.7kPa) to obtain (2-bromoethoxy)benzene.

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