2,3-Dihydrobenzofuran

2,3-Dihydrobenzofuran
  • CAS No.:496-16-2
Other grades of this product :
2,3-Dihydrobenzofuran Basic information
Product Name:2,3-Dihydrobenzofuran
Synonyms:2,3-Dihydro-1-benzofuran;2,3-dihydro-benzofura;Coumaran (2,3-dihydrobenzofuran);Dihydrobenzofuran;Dihydrocoumarone;Kumaran;Benzofuran,2,3-dihydro-;2,3-DIHYDROBENZO[B]FURAN
CAS:496-16-2
MF:C8H8O
MW:120.15
EINECS:207-817-3
Product Categories:Benzodiozoles, Benzodioxines & Benzodioxepines;Fluorobenzene;Benzodiozoles, Benzodioxines & Benzodioxepines;Furan&Benzofuran;bc0001
Mol File:496-16-2.mol
2,3-Dihydrobenzofuran Chemical Properties
Melting point -21°C
Boiling point 188-189 °C (lit.)
density 1.065 g/mL at 25 °C (lit.)
refractive index n20/D 1.549(lit.)
Fp 152 °F
storage temp. Sealed in dry,Room Temperature
solubility alcohol: soluble
form clear liquid
color Colorless to Yellow to Green
Specific Gravity1.065
Merck 14,2559
BRN 111928
InChIKeyHBEDSQVIWPRPAY-UHFFFAOYSA-N
CAS DataBase Reference496-16-2(CAS DataBase Reference)
NIST Chemistry ReferenceBenzofuran, 2,3-dihydro-(496-16-2)
EPA Substance Registry SystemCoumaran (496-16-2)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 23-24/25-26
WGK Germany 3
Hazard Note Irritant
TSCA Yes
HS Code 29329995
MSDS Information
ProviderLanguage
Coumaran English
ACROS English
SigmaAldrich English
ALFA English
2,3-Dihydrobenzofuran Usage And Synthesis
Chemical PropertiesColorless to light yellow liqui
Uses2,3-dihydrobenzofuran is widely used in the synthesis of tricyclic compounds and is also an intermediate raw material for the synthesis of some important drugs. It is used in the synthesis of antitumor agents benzofuran sulfonylureas, HIV protease inhibitor amino acid hydroxyethylenesulfonyl, matrix metalloproteinase inhibitor aryl sulfinyl isoxime hydroxamic acid, etc.
DefinitionChEBI: 2,3-dihydrobenzofuran is a member of the class of 1-benzofurans that is the 2,3-dihydroderivative of benzofuran. It has a role as a metabolite.
General DescriptionBiotransformation of 2,3-dihydrobenzofuran using intact cells of Pseudomonas putida UV4 has been investigated. 2,3-Dihydrobenzofuran is the intermediate formed during catalytic hydrodeoxygenation of benzofuran.

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