CHEBI:39102 - (−)-trans-chrysanthemic acid

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name (−)-trans-chrysanthemic acid
ChEBI ID CHEBI:39102
ChEBI ASCII Name (-)-trans-chrysanthemic acid
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C10H16O2
Net Charge 0
Average Mass 168.23284
Monoisotopic Mass 168.11503
InChI InChI=1S/C10H16O2/c1-6(2)5-7-8(9(11)12)10(7,3)4/h5,7-8H,1-4H3,(H,11,12)/t7-,8+/m0/s1
InChIKey XLOPRKKSAJMMEW-JGVFFNPUSA-N
SMILES CC(C)=C[C@H]1[C@H](C(O)=O)C1(C)C
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
(via chrysanthemic acid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (−)-trans-chrysanthemic acid (CHEBI:39102) is a trans-chrysanthemic acid (CHEBI:39101)
(−)-trans-chrysanthemic acid (CHEBI:39102) is enantiomer of (+)-trans-chrysanthemic acid (CHEBI:39100)
Incoming (−)-trans-allethrin (CHEBI:39120) has functional parent (−)-trans-chrysanthemic acid (CHEBI:39102)
(+)-trans-chrysanthemic acid (CHEBI:39100) is enantiomer of (−)-trans-chrysanthemic acid (CHEBI:39102)
IUPAC Name
(1S,3S)-2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropanecarboxylic acid
Synonyms Sources
(−)-trans-chrysanthemic acid ChemIDplus
(−)-trans-Chrysanthemumsäure ChEBI
(1S-trans)-2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylic acid ChemIDplus
(1S-trans)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylic acid ChemIDplus
l-trans-chrysanthemic acid ChemIDplus
Registry Numbers Types Sources
1862973 Beilstein Registry Number ChemIDplus
2259-14-5 CAS Registry Number ChemIDplus
4904352 Beilstein Registry Number Beilstein
Last Modified
25 December 2007