Structure via PubChem · Public domain (PubChem)
2-methylfuran
Sign in to saveAlso known as 2-Methylfuran (ACD/Name 4.0), Methylfuran, 2-Methylfurane, Sylvan, 2-Methyl-Furan, Methylfuran (DOT), 5-Methylfuran, alpha -Methylfuran
2-Methylfuran, also known with the older name of sylvane, is a flammable, water-insoluble liquid with a chocolate odor, found naturally in Myrtle and Dutch Lavender used as a FEMA GRAS flavoring substance, with the potential for use in alternative fuels.
In the Vinony graph
Within Vinony's link graph, 2-methylfuran is referenced by 11 other articles, and connects out to mass density, digital object identifier and chemical formula.
Vinony files it under 2-Furyl compounds, Biofuels and Chembox image size set.
Its subject is documented across 14 Wikipedia language editions.
Chemical data
- Formula
- C5H6O
- Molecular weight
- 82.1 g/mol
- IUPAC name
- 2-methylfuran
- SMILES
- CC1=CC=CO1
- InChIKey
- VQKFNUFAXTZWDK-UHFFFAOYSA-N
- XLogP
- 1.8
- Polar surface area
- 13.1 Ų
- H-bond donors
- 0
- H-bond acceptors
- 1
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 82.042
Show 5 more facts
- chemical formula
- C₅H₆O
- found in taxon
- Homo sapiens
- canonical SMILES
- CC1=CC=CO1
- melting point
- -89.0
- Commons category
- 2-Methylfuran
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
4 sectionsContents
- Manufacture
- See also
- References
- External links
2-Methylfuran, also known with the older name of sylvane, is a flammable, water-insoluble liquid with a chocolate odor, found naturally in Myrtle and Dutch Lavender used as a FEMA GRAS flavoring substance, with the potential for use in alternative fuels.
==Manufacture== 2-Methylfuran is an article of commerce (chemical intermediate) and is normally manufactured by catalytic hydrogenolysis of furfural alcohol or via a hydrogenation-hydrogenolysis sequence from furfural in the vapor phase.
Excerpted from Wikipedia’s “2-methylfuran” article, available under the CC BY-SA 4.0 licence.