所有图片(2)
About This Item
经验公式（希尔记法）:
C5H10O3
CAS号:
分子量:
118.13
Beilstein:
1721139
MDL编号:
UNSPSC代码:
51113400
PubChem化学物质编号:
NACRES:
NA.22
检测方案
≥98.0% (T)
形式
solid
旋光性
[α]20/D −17±1°, c = 1% in chloroform
mp
64-67 °C
SMILES字符串
CC(C)[C@@H](O)C(O)=O
InChI
1S/C5H10O3/c1-3(2)4(6)5(7)8/h3-4,6H,1-2H3,(H,7,8)/t4-/m1/s1
InChI key
NGEWQZIDQIYUNV-SCSAIBSYSA-N
应用
D-α-Hydroxyisovaleric acid may be used in the preparation of biodegradable, optically active and isotactic poly(D-2-hydroxy-3-methylbutanoic acid).
其他说明
该手性 α-羟基酸用于合成肽和缩酚酸肽。 还可用作手性结构单元。 通过二氧戊环酮中间体合成 α-取代 α-羟基酸。
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
R L Johnson
Journal of medicinal chemistry, 23(6), 666-669 (1980-06-01)
The following N-(alpha-hydroxylakanoyl) derivatives of Leu-Val-Phe-OCH3 were synthesized and tested for their ability to inhibit human amniotic renin: D- and L-alpha-hydroxyisocaproyl-Leu-Val-Phe-OCH3, D- and L-alpha-hydroxyisovaleryl-Leu-Val-Phe-OCH3, L-2-hydroxy-3-phenylpropanoyl-Leu-Val-Phe-OCH3, and D- and L-alpha-hydroxyphenylacetyl-Leu-Val-Phe-OCH3. Analysis of the compounds through the use of Dixion plots showed
H.-O. Kim et al.
The Journal of Organic Chemistry, 52, 4531-4531 (1987)
W. Hartwig et al.
Liebigs Ann. Chem., 1952-1952 (1982)
Hetero-stereocomplex formation between substituted poly (lactic acid) s with linear and branched side chains, poly (l-2-hydroxybutanoic acid) and poly (d-2-hydroxy-3-methylbutanoic acid).
Tsuji H and Hayakawa T.
Polymer, 55(3), 721-726 (2014)
Biotinidase deficiency: metabolites in CSF.
A Fois et al.
Journal of inherited metabolic disease, 9(3), 284-285 (1986-01-01)
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