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| Formula | C5H6O2 |
| Net Charge | 0 |
| Average Mass | 98.101 |
| Monoisotopic Mass | 98.03678 |
| SMILES | OCc1ccco1 |
| InChI | InChI=1S/C5H6O2/c6-4-5-2-1-3-7-5/h1-3,6H,4H2 |
| InChIKey | XPFVYQJUAUNWIW-UHFFFAOYSA-N |
| Wikipedia |
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| Roles Classification |
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| Chemical Role: | Maillard reaction product Any thermal degradation product obtained as a result of a chemical reaction between an amino acid and a reducing sugar (Maillard reaction, a non-enzymatic browning procedure that usually imparts flavour to starch-based food products). |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| furfuryl alcohol (CHEBI:207496) has role Maillard reaction product (CHEBI:77523) |
| furfuryl alcohol (CHEBI:207496) is a furans (CHEBI:24129) |
| furfuryl alcohol (CHEBI:207496) is a primary alcohol (CHEBI:15734) |
| Incoming Relation(s) |
| furfuryl group (CHEBI:55311) is substituent group from furfuryl alcohol (CHEBI:207496) |
| IUPAC Name |
|---|
| furan-2-ylmethanol |
| Synonyms | Source |
|---|---|
| Furan-2-yl-methanol | ChEMBL |
| 2-Furancarbinol | ChemIDplus |
| 2-Furanmethanol | NIST Chemistry WebBook |
| 2-Furanylmethanol | ChemIDplus |
| 2-Furfuryl alcohol | ChemIDplus |
| 2-Furylcarbinol | ChemIDplus |
| Manual Xrefs | Databases |
|---|---|
| C20441 | KEGG COMPOUND |
| CPD-14102 | MetaCyc |
| HMDB0013742 | HMDB |
| Furfuryl_alcohol | Wikipedia |
| Citations |
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