Type : Lactone, Natural, Pheromone, Hexadecanoate, Palmitate
Chemical_Nomenclature : 6-undecyloxan-2-one
Canonical SMILES : CCCCCCCCCCCC1CCCC(=O)O1
InChI : InChI=1S\/C16H30O2\/c1-2-3-4-5-6-7-8-9-10-12-15-13-11-14-16(17)18-15\/h15H,2-14H2,1H3
InChIKey : ZMJKQSSFLIFELJ-UHFFFAOYSA-N
Other name(s) : 6-undecyloxan-2-one || 5-Hydroxyhexadecanoic acid lactone || 5-Hexadecanolide || Tetrahydro-6-undecyl-2H-pyran-2-one
MW : 254.41
Formula : C16H30O2
CAS_number : 7370-44-7
PubChem : 110976
UniChem : ZMJKQSSFLIFELJ-UHFFFAOYSA-N
Structures : No structure
Families : Canar_LipB
Title : Combination of Novozym 435-catalyzed enantioselective hydrolysis and amidation for the preparation of optically active delta-hexadecalactone - Shimotori_2015_J.Oleo.Sci_64_561 |
Author(s) : Shimotori Y , Hoshi M , Miyakoshi T |
Ref : J Oleo Sci , 64 :561 , 2015 |
Abstract : |
PubMedSearch : Shimotori_2015_J.Oleo.Sci_64_561 |
PubMedID: 25948138 |
Gene_locus related to this paper: canar-LipB |