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1708-41-4

1708-41-4 Structure

1708-41-4 Structure
IdentificationBack Directory
[Name]

2-(1,3-DIOXOLAN-2-YL)FURAN
[CAS]

1708-41-4
[Synonyms]

Furalane
RARECHEM AL BP 0007
2-Furyl-1,3-dioxolane
FURFURAL ETHYLENE ACETAL
2-(2-FURYL)-1,3-DIOXOLANE
2-(1,3-DIOXOLAN-2-YL)FURAN
2-(furan-2-yl)-1,3-dioxolane
2-(1,3-Dioxolan-2-yl)furan>
1,3-Dioxolane, 2-(2-furanyl)-
2-Furfural ethylene glycol acetal
Furfural Ethylene Acetal 2-(2-Furyl)-1,3-dioxolane
(1E)-N-(methylcarbamoyloxy)ethanimidothioic acid methyl ester
[Molecular Formula]

C7H8O3
[MDL Number]

MFCD00671520
[MOL File]

1708-41-4.mol
[Molecular Weight]

140.14
Chemical PropertiesBack Directory
[Melting point ]

-41 °C
[Boiling point ]

76°C/1mmHg(lit.)
[density ]

1,2 g/cm3
[refractive index ]

1.4840-1.4870
[storage temp. ]

?20°C
[form ]

clear liquid
[color ]

Colorless to Light orange to Yellow
[InChI]

InChI=1S/C7H8O3/c1-2-6(8-3-1)7-9-4-5-10-7/h1-3,7H,4-5H2
[InChIKey]

FCACHSUJEMZCMK-UHFFFAOYSA-N
[SMILES]

O1CCOC1C1=CC=CO1
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H227
[Precautionary statements ]

P210-P280-P403+P235-P501
[HS Code ]

2932190090
Hazard InformationBack Directory
[Production Methods]

Confirmed industrial routes are not available in open literature. However, industrial manufacture of furalane would probably follow the standard acetalisation process used for many 1,3 dioxolanes: furfural is reacted with ethylene glycol under acid catalysis, typically using a mineral acid or solid acid catalyst, while continuously removing water to drive the equilibrium toward acetal formation. After completion, the reaction mixture would be neutralised, washed, and distilled to yield technical grade furalane suitable for formulation.
[Pesticide Type]

Plant Growth Regulator
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