55201
DL-泛酰内酯
purum, ≥97.0% (T)
别名:
β,β-二甲基-α-羟基-γ-丁内酯, DL-泛解酸内酯, 二氢-3-羟基-4,4-二甲基-2(3H)-呋喃酮
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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
Beilstein:
80958
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
等级
purum
质量水平
方案
≥97.0% (T)
表单
solid
mp
74-78 °C (lit.)
溶解性
H2O: 1 g/10 mL, clear, colorless to almost colorless
官能团
ester
hydroxyl
SMILES字符串
CC1(C)COC(=O)C1O
InChI
1S/C6H10O3/c1-6(2)3-9-5(8)4(6)7/h4,7H,3H2,1-2H3
InChI key
SERHXTVXHNVDKA-UHFFFAOYSA-N
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应用
DL-α-羟基-β,β-二甲基-γ-丁内酯（DL-泛内酯）可用于制备 3,5-二硝基苯甲酰基-DL-泛内酯。
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2
储存分类代码
11 - Combustible Solids
WGK
WGK 1
闪点(°F)
251.6 °F - open cup
闪点(°C)
122 °C - open cup
个人防护装备
Eyeshields, Gloves, type N95 (US)
The Bacterial Degradation of Pantothenic Acid. III. Enzymatic Formation of Aldopantoic Acid*.
Goodhue CT and Snell EE.
Biochemistry, 5(2), 403-408 (1966)
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
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)
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
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
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