ChemicalBook--->CAS DataBase List--->523-80-8

523-80-8

523-80-8 Structure

523-80-8 Structure
IdentificationBack Directory
[Name]

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

523-80-8
[Synonyms]

APIOL
APIOLE
NSC9070
NSC-9070
NSC 9070
Apioline
parsleyapiol
parsleycamphor
PARSLEY APIOLE
APIOLE WITH GC
Parsley camphor
apiole (parsley)
Petersilienapiol
Camphre de Persil
Petersiliencampher
2,5-dimethoxysafrole
APIOLE; PETERSILIENCAMPHER
5-ALLYL-4,7-DIMETHOXY-1,3-BENZODIOXOLE
5-allyl-4,7-dimethoxy-benzo-1,3-dioxole
4,7-dimethoxy-5-(2-propenyl)-3-benzodioxole
4,7-dimethoxy-5-propan-2-yl-1,3-benzodioxole
4,7-dimethoxy-5-prop-2-enyl-1,3-benzodioxole
4,7-DIMETHOXY-5-(2-PROPANYL)-1,3-BENZODIOXOLE
4,7-DIMETHOXY-5-(2-PROPENYL)-1,3-BENZODIOXOLE
1,3-Benzodioxole, 4,7-dimethoxy-5-(2-propenyl)-
1-allyl-2,5-dimethoxy-3,4-methylenedioxybenzene
1-allyl-2,5-dimethoxy-3,4-(methylenedioxy)-benzen
1-Allyl-2,5-dimethoxy-3,4-(methylenedioxy)benzene
benzene,1-allyl-2,5-dimethoxy-3,4-(methylenedioxy)-
Benzene, 1-allyl-2,5-dimethoxy-3,4-(methylenedioxy)-
[EINECS(EC#)]

208-349-2
[Molecular Formula]

C12H14O4
[MDL Number]

MFCD00047270
[MOL File]

523-80-8.mol
[Molecular Weight]

222.24
Chemical PropertiesBack Directory
[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)
Safety DataBack Directory
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36/37/39
Hazard InformationBack Directory
[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.
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