Product Name: 3-Bromofuran
Synonyms: 3-BroMofuran, stabilized with Cu(0.1%), Furan (0.5%) & NaHCO3 (0.4%), 95%;3-Bromofuran 97%;3-BROMOFURAN;BUTTPARK 98\57-04;BETA-BROMOFURAN;TIMTEC-BB SBB004098;3-bromofurane;3-Bromofuran99%
CAS: 22037-28-1
MF: C4H3BrO
MW: 146.97
EINECS: 244-744-6
Product Categories: HALIDE;Furans, Benzofurans & Dihydrobenzofurans;Halides;Furan&Benzofuran;Heterocyclic Compounds;Furans;Furans, Benzofurans & Dihydrobenzofurans;Heterocycles;Building Blocks;FuransHeterocyclic Building Blocks;Halogenated Heterocycles;Heterocyclic Building Blocks
Mol File: 22037-28-1.mol
3-Bromofuran Structure
3-Bromofuran Chemical Properties
Melting point 131.5-132 °C
Boiling point 103 °C(lit.)
density 1.635 g/mL at 25 °C(lit.)
refractive index n20/D 1.496(lit.)
Fp 38 °F
storage temp. −20°C
form Liquid
color Clear yellow to orange to brown
Water Solubility Soluble in chloroform, ethyl acetate. Insoluble in water.
BRN 105337
InChIKey LXWLEQZDXOQZGW-UHFFFAOYSA-N
CAS DataBase Reference 22037-28-1(CAS DataBase Reference)
NIST Chemistry Reference Furan, 3-bromo-(22037-28-1)
Safety Information
Hazard Codes F,Xi
Risk Statements 11-36/37/38
Safety Statements 16-23-24/25-37/39-26-33-29-7/9
RIDADR UN 1993 3/PG 2
WGK Germany 3
F 10
Hazard Note Highly Flammable/Irritant
HazardClass 3
PackingGroup II
HS Code 29321900
MSDS Information
Provider Language
3-Bromofuran English
SigmaAldrich English
ACROS English
ALFA English
3-Bromofuran Usage And Synthesis
Chemical Properties Colorless to light yellow liqui
Uses 3-Bromofuran is heterocyclic building block used in organic synthesis. 3-Bromofuran is one of the volatile metabolites discussed in studies for detecting and discriminating diseases of onion.
Purification Methods Purify 3-bromofuran by two steam distillations and dry it over fresh CaO. It can be dried over Na metal (no obvious reaction) and fractionated. It is not very soluble in H2O but is soluble in organic solvents. When freshly distilled, it is a clear oil, but darkens on standing and eventually resinifies. It can be stored for long periods by covering the oil with an alkaline solution of hydroquinone and is redistilled when required. It forms a characteristic maleic anhydride adduct, m 131.5-132o. [Shepard et al. J Am Chem Soc 52 2083 1930, Huhes & Johnson J Am Chem Soc 53 737 1931, adduct: van Campen & Johnson J Am Chem Soc 55 430 1933, Beilstein 17/1 V 295.]
China
