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3-COUMARANONE

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3-COUMARANONE Basic information

Product Name:
3-COUMARANONE
Synonyms:
  • 3-Oxocoumaran
  • 3-Coumaranonebenzofuran-3(2H)-one
  • Benzo[b]furan-3(2H)-one
  • 1-Benzofuran-3(2H)-one
  • 1-Benzofuran-3(2H)-one, Coumaran-3-one
  • 2,3-dihydro-1-benzofuran-2-one
  • 1-Benzofuran-3(2H)-one, Coumaran-3-one, 2,3-Dihydro-3-oxo-1-benzofuran
  • Benzofuran-3(2H)-one >=98.0% (HPLC)
CAS:
7169-34-8
MF:
C8H6O2
MW:
134.13
EINECS:
640-279-1
Product Categories:
  • Benzofurans
  • Building Blocks
  • pharmacetical
  • Fused Ring Systems
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Furan&Benzofuran
Mol File:
7169-34-8.mol
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3-COUMARANONE Chemical Properties

Melting point:
101-103 °C
Boiling point:
207.23°C (rough estimate)
Density 
1.1603 (rough estimate)
refractive index 
1.4800 (estimate)
storage temp. 
Keep in dark place,Sealed in dry,Store in freezer, under -20°C
solubility 
Chloroform (Slightly), DMSO (Slightly)
form 
Solid
color 
Yellow to Dark Yellow
Water Solubility 
Slightly miscible with water.
Sensitive 
Light Sensitive
BRN 
115296
CAS DataBase Reference
7169-34-8(CAS DataBase Reference)
NIST Chemistry Reference
3(2H)-benzofuranone(7169-34-8)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-20/21/22
Safety Statements 
22-24/25-36/37/39-26-36
WGK Germany 
3
4.5-9
Hazard Note 
Irritant
HS Code 
29329990

MSDS

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3-COUMARANONE Usage And Synthesis

Chemical Properties

white to light yellow crystal powde

Uses

3-Coumaranone is used in the aurones, [2-benzylidenebenzofuran-3(2H)-ones] by reacting with appropriate aldehyde. It is involved in the condensation reaction with aldehydes in the presence of morpholine acetate to prepare substituted 2-(arylidene)benzofuran-3(ZH)-ones. In Horner-Wadsworth-Emmons reaction, it reacts with diethyl? cyanomethyl?phosphonate to give 3-(cyanomethyl)benzofurans, which is an intermediate in the synthesis of antihyperglycemic agents.

General Description

Benzofuran-3(2H)-one undergoes condensation with aldehydes in the presence of morpholine acetate to yield substituted 2-(arylidene)benzofuran-3(ZH)-ones. It undergoes acid- or base-catalyzed condensation with an appropriate aldehyde to yield aurones [2-benzylidenebenzofuran-3(2H)-ones].

3-COUMARANONESupplier

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