| Identification | Back 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 Properties | Back 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 |
| Hazard Information | Back 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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Energy Chemical
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021-021-58432009 400-005-6266 |
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http://www.energy-chemical.com |
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TCI Europe
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320-37350700 |
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https://www.tcichemicals.com/de/de/index.html |
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