28730
环十二酮
purum, ≥99.0% (GC)
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线性分子式:
C12H22(=O)
化学文摘社编号:
分子量:
182.30
EC Number:
212-595-6
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
508621
MDL number:
grade
purum
assay
≥99.0% (GC)
bp
85 °C/1 mmHg (lit.)
mp
59-61 °C
density
0.906 g/mL at 25 °C (lit.)
SMILES string
O=C1CCCCCCCCCCC1
InChI
1S/C12H22O/c13-12-10-8-6-4-2-1-3-5-7-9-11-12/h1-11H2
InChI key
SXVPOSFURRDKBO-UHFFFAOYSA-N
General description
The expediancy of the bioproduction of lauryl lactone from cyclododecanone was examined.
Application
Cyclododecanone was used in the synthesis of novel macrocyclic molecules comprising sulfonyl and acyl moiety at the position N-12a of 16-membered azalides and azalactams scaffold.
法规信息
新产品
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Xiaolei Wang et al.
European journal of medicinal chemistry, 73, 286-294 (2014-01-29)
Novel macrocyclic molecules comprising sulfonyl and acyl moiety at the position N-12a of 16-membered azalides (6a-n) and azalactams (10a-r) scaffold were synthesized from cyclododecanone 1 as starting material via 5 steps and 4 steps, respectively. The antifungal activity of these
Jianzhong Yang et al.
Applied microbiology and biotechnology, 84(5), 867-876 (2009-05-16)
Recombinant Escherichia coli whole-cell biocatalysts harboring either a Baeyer-Villiger monooxygenase or ferulic acid decarboxylase were employed in organic-aqueous two-phase bioreactor systems. The feasibility of the bioproduction of water-insoluble products, viz., lauryl lactone from cyclododecanone and 4-vinyl guaiacol from ferulic acid
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