729698
(S)-(+)-泛酸内酯
97%
别名:
(S)-(+)-α-羟基-β,β-二甲基-γ-丁内酯, (S)-(+)-β,β-二甲基-α-羟基-γ-丁内酯, (S)-二氢-3-羟基-4,4-二甲基-2(3H)-呋喃酮, L-泛内酯
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关于此项目
经验公式（希尔记法）:
C6H10O3
化学文摘社编号:
分子量:
130.14
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4659425
Assay:
97%
Form:
crystals
InChI key
SERHXTVXHNVDKA-SCSAIBSYSA-N
InChI
1S/C6H10O3/c1-6(2)3-9-5(8)4(6)7/h4,7H,3H2,1-2H3/t4-/m1/s1
SMILES string
CC1(C)COC(=O)[C@H]1O
assay
97%
form
crystals
optical activity
[α]22/D +50.0°, c = 0.5 in H2O
bp
120-122 °C/15 mmHg (lit.)
mp
89-93 °C
functional group
ester, hydroxyl
storage temp.
2-8°C
Quality Level
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
R K Airas
The Biochemical journal, 250(2), 447-451 (1988-03-01)
A pseudomonad was separated having a pantothenase that produced beta-alanine and pantoic acid. The pantothenase from an old strain, Pseudomonas fluorescens UK-1, was shown to produce beta-alanine and pantoyl lactone. The pantoic acid-producing pantothenase was characterized and compared with the
Total synthesis and antitumor activity of ZK-EPO: the first fully synthetic epothilone in clinical development.
Ulrich Klar et al.
Angewandte Chemie (International ed. in English), 45(47), 7942-7948 (2006-09-29)
A D Keefe et al.
Nature, 373(6516), 683-685 (1995-02-23)
The involvement of coenzyme A in many enzyme reactions suggests that it acted in this capacity very early in the development of life on Earth. Particularly relevant in this regard is its role in the activation of amino acids and
Michael-Rock Goldsmith et al.
Journal of the American Chemical Society, 125(51), 15696-15697 (2003-12-18)
Dilute solutions of (R)-(-)-pantolactone in CCl4 were studied by polarimetry in conjunction with theoretical calculations of [alpha]D. Our data demonstrate that the self-association of a chiral solute results in a change in [alpha]D that can be accounted for by the
Zhiqiang Liu et al.
Journal of agricultural and food chemistry, 54(16), 5823-5830 (2006-08-03)
D-Pantonohydrolase has attracted increasing attention as a biocatalyst for stereospecific production of D-pantoic acid. The Fusarium moniliforme D-pantonohydrolase was selected for directed evolution through error-prone Polymerase Chain Reaction (PCR) combined with DNA shuffling for improved activity and pH stability using
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