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Substrate Report for: Hexadecalactone

General
Type Lactone, Ring opening polymerization substrate, Hexadecanoate
Chemical_Nomenclature oxacycloheptadecan-2-one
Canonical SMILES C1CCCCCCCC(=O)OCCCCCCC1
InChI InChI=1S/C16H30O2/c17-16-14-12-10-8-6-4-2-1-3-5-7-9-11-13-15-18-16/h1-15H2
InChIKey LOKPJYNMYCVCRM-UHFFFAOYSA-N
Other name(s) 16-Hexadecanolide ; Hexadecanolide ; hexadecanolactone ; omega-hexadecalactone ; Dihydroambrettolide ; 16-Hexadecanolactone ; SCHEMBL111372 ; CHEMBL3189021 ; ZINC3875762 ; 1,16-Hexadecanolide ; Oxacycloheptadecan-2-one ; Juniperic acid lactone ; Hexadecanoic acid, 16-hydroxy-, .omicron.-lactone
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MW|254.41
Formula|C16H30O2
CAS_number|109-29-5
PubChem|7984
UniChem|LOKPJYNMYCVCRM-UHFFFAOYSA-N
IUPHAR|
Wikipedia|

Target

References:
Search PubMed for references concerning: Hexadecalactone
    Title: Exploring the Solid State Properties of Enzymatic Poly(amine-co-ester) Terpolymers to Expand their Applications in Gene Transfection
    Voevodina I, Scandola M, Zhang J, Jiang Z
    Ref: RSC Adv, 4:8953, 2014 : PubMed

            

    Title: Polymers from functional macrolactones as potential biomaterials: enzymatic ring opening polymerization, biodegradation, and biocompatibility
    van der Meulen I, de Geus M, Antheunis H, Deumens R, Joosten EA, Koning CE, Heise A
    Ref: Biomacromolecules, 9:3404, 2008 : PubMed

            

    Title: A comparison of lipase-catalysed ester and lactone synthesis in low-water systems: analysis of optimum water activity
    Alston MJ, Freedman RB
    Ref: Biotechnol Bioeng, 77:641, 2002 : PubMed