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4,7-DIMETHOXY-5-(2-PROPANYL)-1,3-BENZODIOXOLE

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4,7-DIMETHOXY-5-(2-PROPANYL)-1,3-BENZODIOXOLE Basic information

Product Name:
4,7-DIMETHOXY-5-(2-PROPANYL)-1,3-BENZODIOXOLE
Synonyms:
  • 5-ALLYL-4,7-DIMETHOXY-1,3-BENZODIOXOLE
  • 4,7-DIMETHOXY-5-(2-PROPANYL)-1,3-BENZODIOXOLE
  • 4,7-DIMETHOXY-5-(2-PROPENYL)-1,3-BENZODIOXOLE
  • APIOL
  • APIOLE
  • PARSLEY APIOLE
  • 1,3-Benzodioxole, 4,7-dimethoxy-5-(2-propenyl)-
  • 2,5-dimethoxysafrole
CAS:
523-80-8
MF:
C12H14O4
MW:
222.24
EINECS:
208-349-2
Mol File:
523-80-8.mol
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4,7-DIMETHOXY-5-(2-PROPANYL)-1,3-BENZODIOXOLE Chemical Properties

Melting point:
29°C
Boiling point:
294°C
Density 
1.0150
refractive index 
nD20 1.536-1.538
Odor
at 100.00 %. parsley faint
Odor Type
herbal
LogP
3.481 (est)
EPA Substance Registry System
1,3-Benzodioxole, 4,7-dimethoxy-5-(2-propenyl)- (523-80-8)
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
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4,7-DIMETHOXY-5-(2-PROPANYL)-1,3-BENZODIOXOLE Usage And Synthesis

Chemical Properties

Apiole is a colorless crystal needles. M.P. 30℃. Once liquefied, it may remain supercooled for a considerable length of time. B.P. 298° C. Sp.Gr. 1.17 (liquid). Insoluble in water.

Uses

antipyretic, diuretic, insecticide

Uses

Apioline is extracted from essential oil from the roots of Illicium Ianceolatum and is known to exhibit antinociceptive and anti-inflammatory properties.

Definition

ChEBI: Apiole is a member of benzodioxoles. It has a role as a metabolite.

Preparation

Apiole is prepared isolation from Parsley seed oil, containing 70-80% Apiole. 2) it is synthesized from 2-Hydroxy-3,4-methy lenedioxy-1-allyl benzene by oxidation followed by methylation.

4,7-DIMETHOXY-5-(2-PROPANYL)-1,3-BENZODIOXOLESupplier

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