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质量水平
检测方案
98%
旋光性
[α]20/D −10°, neat
折射率
n20/D 1.386 (lit.)
bp
63 °C (lit.)
密度
0.837 g/mL at 25 °C (lit.)
SMILES字符串
CC[C@H]1CO1
InChI
1S/C4H8O/c1-2-4-3-5-4/h4H,2-3H2,1H3/t4-/m0/s1
InChI key
RBACIKXCRWGCBB-BYPYZUCNSA-N
应用
(S)-(−)-1,2-Epoxybutane can be used:
- As a starting material to prepare (+)- and (−)-homononactic acids, which are used as intermediates in the total synthesis of a cyclic antibiotic tetranactin.
- To prepare a chiral phosphorus synthon, which is applicable in the synthesis of phytoprostane B1 type I.
- To prepare Eu3+-based precatalysts applicable in the Mukaiyama Aldol reaction in water.
法律信息
经 Shasun Chemicals and Drugs Limited 授权,使用 Jacobsen HKR 技术制造。
警示用语:
Danger
危险分类
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B
WGK
WGK 3
闪点(°F)
10.0 °F
闪点(°C)
-12.2 °C
个人防护装备
Faceshields, Gloves, Goggles
法规信息
新产品
A flexible synthesis of the phytoprostanes B1 type I and II
The Journal of Organic Chemistry, 70(3), 989-997 (2005)
Synthesis, spectroscopic characterization, and reactivity of water-tolerant Eu3+-based precatalysts
Inorganic Chemistry, 53(12), 6257-6263 (2014)
Synthesis of (+)-and (−)-homononactic acid from (S)-1, 2-epoxybutane. Total synthesis of tetranactin by ′reverse coupe du roi′
Journal of the Chemical Society. Chemical Communications, 996-998 (1986)
Journal of environmental pathology and toxicology, 3(5-6), 171-187 (1980-06-01)
Nitrosopiperidine, sodium nitrite and 1,2 epoxybutane were tested in the Ames agar incorporation assay in an attempt to establish exact criteria for detecting the activity of these weak mutagens. As regards minimum concentrations it was determined that at 500 microgram
1,2-Epoxybutane.
IARC monographs on the evaluation of carcinogenic risks to humans, 47, 217-228 (1989-01-01)
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