55200
D-(−)-泛内酯
puriss., ≥99.0% (T)
别名:
(R)-(−)-α-羟基-β,β-二甲基-γ-丁内酯, (R)-(−)-β,β-二甲基-α-羟基-γ-丁内酯, (R)-(−)-泛内酯, 泛解酸 γ-内酯
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经验公式（希尔记法）:
C6H10O3
化学文摘社编号:
分子量:
130.14
EC Number:
209-963-3
UNSPSC Code:
12352005
PubChem Substance ID:
Beilstein/REAXYS Number:
80957
MDL number:
InChI key
SERHXTVXHNVDKA-BYPYZUCNSA-N
InChI
1S/C6H10O3/c1-6(2)3-9-5(8)4(6)7/h4,7H,3H2,1-2H3/t4-/m0/s1
SMILES string
CC1(C)COC(=O)[C@@H]1O
grade
puriss.
assay
≥99.0% (T)
form
solid
optical activity
[α]20/D −51±2°, c = 3% in H2O
bp
120-122 °C/15 mmHg (lit.)
mp
89-92 °C, 91 °C (lit.)
storage temp.
2-8°C
Other Notes
用作手性结构单元：还原成三醇；酰胺化；简便地获得环氧乙烷的两种对映体：S(+)- 和 R(-)-2,2-二甲基-3,4-环氧丁醇
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
R.E. Dolle et al.
Journal of the American Chemical Society, 107, 1691-1691 (1985)
P. Lavallee et al.
Tetrahedron Letters, 27, 679-679 (1986)
G.C. Fischer et al.
The Journal of Organic Chemistry, 50, 2011-2011 (1985)
S L Miller et al.
Journal of molecular evolution, 36(4), 308-314 (1993-04-01)
Pantoic acid can by synthesized in good prebiotic yield from isobutyraldehyde or alpha-ketoisovaleric acid + H2CO + HCN. Isobutyraldehyde is the Strecker precursor to valine and alpha-ketoisovaleric acid is the valine transamination product. Mg2+ and Ca2+ as well as several
Optical resolution of pantolactone by a novel fungal enzyme, lactonohydrolase.
S Shimizu et al.
Annals of the New York Academy of Sciences, 799, 650-658 (1996-10-12)
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