推荐产品
质量水平
检测方案
≥95.0% (sum of enantiomers, GC)
旋光性
[α]20/D −6.3±0.5°, c = 10% in ethanol
折射率
n/D 1.41
n20/D 1.411
bp
129-131 °C (lit.)
密度
0.819 g/mL at 20 °C (lit.)
0.811 g/mL at 25 °C
储存温度
2-8°C
SMILES字符串
CC[C@H](C)CO
InChI
1S/C5H12O/c1-3-5(2)4-6/h5-6H,3-4H2,1-2H3/t5-/m0/s1
InChI key
QPRQEDXDYOZYLA-YFKPBYRVSA-N
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一般描述
主要剩余异戊醇
应用
(S)-(-)-2-Methylbutanol can be used as a reactant to prepare:
- Methylbutyl-2-(3-thienyl)acetate (MBTA) by esterification reaction with 3-thiophene acetic acid in the presence of an acid catalyst.
- (2S)-2-Methyl-1-butanesulfenyl chloride by reacting with thioacetic acid using Mitsunobu reaction conditions.
- (+)-Violapyrone C and (-)-myxalamide A.
警示用语：
Warning
危险声明
危险分类
Acute Tox. 4 Inhalation - Flam. Liq. 3 - STOT SE 3
靶器官
Respiratory system
补充剂危害
WGK
WGK 3
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
Total Synthesis and Configurational Validation of (+)-Violapyrone C
Lee JS, et al.
European Journal of Organic Chemistry, 2014(21), 4472-4476 (2014)
Concise Total Synthesis of (-)-Myxalamide A
Fujita K et al.
Angewandte Chemie (International ed. in English), 51(29), 7271-7274 (2012)
Synthesis and Characterization of Conducting Copolymers of (S)-2-Methylbutyl-2-(3-thienyl) acetate with Pyrrole and Thiophene
Levent A, et al.
Macromolecular Chemistry and Physics, 204(8), 1118-1122 (2003)
A general method for the enantiospecific synthesis of optically active aliphatic sulfenyl chlorides and thiophthalimides
Cevasco G, et al.
Tetrahedron Asymmetry, 1(3), 141-142 (1990)
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