CHEBI:2091 - 5-methyl-2-furaldehyde

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 5-methyl-2-furaldehyde
ChEBI ID CHEBI:2091
Definition A member of the class of furans that is furan which is substituted at positions 2 and 5 by formyl and methyl groups, respectively.
Stars This entity has been manually annotated by a third party.
Supplier Information
Download Molfile XML SDF
Formula C6H6O2
Net Charge 0
Average Mass 110.112
Monoisotopic Mass 110.03678
InChI InChI=1S/C6H6O2/c1-5-2-3-6(4-7)8-5/h2-4H,1H3
InChIKey OUDFNZMQXZILJD-UHFFFAOYSA-N
SMILES [H]C(=O)C1=CC=C(C)O1
Metabolite of Species Details
Homo sapiens (NCBI:txid9606) Found in faeces (UBERON:0001988). See: PubMed
Roles Classification
Chemical Role(s): 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).
Biological Role(s): human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
EC 2.2.1.6 (acetolactate synthase) inhibitor
An EC 2.2.1.* (transketolase/transaldolase) inhibitor that interferes with the action of acetolactate synthase (EC 2.2.1.6).
flavouring agent
A food additive that is used to added improve the taste or odour of a food.
Application(s): flavouring agent
A food additive that is used to added improve the taste or odour of a food.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 5-methyl-2-furaldehyde (CHEBI:2091) has role EC 2.2.1.6 (acetolactate synthase) inhibitor (CHEBI:22180)
5-methyl-2-furaldehyde (CHEBI:2091) has role flavouring agent (CHEBI:35617)
5-methyl-2-furaldehyde (CHEBI:2091) has role human metabolite (CHEBI:77746)
5-methyl-2-furaldehyde (CHEBI:2091) has role Maillard reaction product (CHEBI:77523)
5-methyl-2-furaldehyde (CHEBI:2091) is a aldehyde (CHEBI:17478)
5-methyl-2-furaldehyde (CHEBI:2091) is a furans (CHEBI:24129)
IUPAC Name
5-methylfuran-2-carbaldehyde
Synonyms Sources
2-formyl-5-methylfuran ChemIDplus
2-methyl-5-formylfuran ChemIDplus
5-methyl furfural ChemIDplus
5-methyl-2-furanaldehyde NIST Chemistry WebBook
5-methyl-2-furancarbaldehyde NIST Chemistry WebBook
5-methyl-2-furancarboxaldehyde ChemIDplus
5-methyl-2-furancarboxyaldehyde NIST Chemistry WebBook
5-methyl-2-furfural ChemIDplus
5-methyl-2-furfuraldehyde ChemIDplus
5-methyl-furfural HMDB
5-methylfuran-2-al ChemIDplus
5-methylfurfural ChemIDplus
5-methylfurfuraldehyde ChemIDplus
alpha-Methylfurfural HMDB
FEMA 2702 HMDB
methyl-5-furfural NIST Chemistry WebBook
Manual Xrefs Databases
11600 ChemSpider
C11115 KEGG COMPOUND
CN1939914 Patent
EP0044186 Patent
FDB010991 FooDB
HMDB0033002 HMDB
View more database links
Registry Numbers Types Sources
106895 Reaxys Registry Number Reaxys
620-02-0 CAS Registry Number NIST Chemistry WebBook
620-02-0 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
10552780 PubMed citation Europe PMC
14584699 PubMed citation Europe PMC
17314143 PubMed citation Europe PMC
19531891 PubMed citation Europe PMC
21394924 PubMed citation Europe PMC
26871887 PubMed citation Europe PMC
30191924 PubMed citation Europe PMC
30315683 PubMed citation Europe PMC
31387211 PubMed citation Europe PMC
3188569 PubMed citation Europe PMC
33500400 PubMed citation Europe PMC
5956986 PubMed citation Europe PMC
Last Modified
21 June 2021