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经验公式(希尔记法):
C10H18O2
化学文摘社编号:
分子量:
170.25
UNSPSC Code:
12352000
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2325340
Assay:
≥97.0% (GC)
Form:
solid
InChI
1S/C10H18O2/c1-7(2)8-4-5-10(3,12)9(11)6-8/h8-9,11-12H,1,4-6H2,2-3H3/t8-,9+,10+/m1/s1
SMILES string
O[C@@H]1[C@@](C)(O)CC[C@@H](C(C)=C)C1
InChI key
WKZWTZTZWGWEGE-UTLUCORTSA-N
assay
≥97.0% (GC)
form
solid
optical activity
[α]/D +45±5°, c = 1 in acetone
General description
(1S,2S,4R)-(+)-Limonene-1,2-diol is formed during the biocatalytic oxidation of (4R)-(+)-limonene by chloroperoxidase (CPO) extracted from Caldariomyces fumago.
Stereoselective oxidation of R-(+)-limonene by chloroperoxidase from Caldariomyces fumago.
Aguila S, et al.
Green Chemistry, 10(6), 647-653 (2008)
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