所有图片(1)
About This Item
线性分子式:
C2H5CH(NH2)CH3
CAS号:
分子量:
73.14
Beilstein:
1718761
EC 号:
MDL编号:
UNSPSC代码:
12352116
PubChem化学物质编号:
NACRES:
NA.22
质量水平
检测方案
99%
旋光性
[α]19/D −7.5°, neat
折射率
n20/D 1.393 (lit.)
bp
63 °C (lit.)
密度
0.72 g/mL at 25 °C (lit.)
SMILES字符串
CC[C@@H](C)N
InChI
1S/C4H11N/c1-3-4(2)5/h4H,3,5H2,1-2H3/t4-/m1/s1
InChI key
BHRZNVHARXXAHW-SCSAIBSYSA-N
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应用
(R)-(−)-sec-Butylamine can be used:
- To prepare (R)-(−)-sec-butylbis(2-hydroxyethyl)amine, an intermediate for the synthesis of aminodiphosphine ligands.
- As a substrate to demonstrate the stereochemistry of Mitsunobu reaction in the synthesis of secondary amines.
- As a model compound in the study of singlet-triplet transitions in circular dichroism.
包装
Bottomless glass bottle. Contents are inside inserted fused cone.
警示用语：
Danger
危险分类
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A
WGK
WGK 3
闪点(°F)
-2.2 °F
闪点(°C)
-19 °C
个人防护装备
Faceshields, Gloves, Goggles
法规信息
农药列管产品
危险化学品
Detection of singlet-triplet transitions in circular dichroism. A study of 2-aminobutane
Basil A and Gedanken A
Journal of the American Chemical Society, 111(26), 9237-9238 (1989)
Synthesis of the New Chiral (R)-and (S)-Aminodiphosphine Ligands sec-Butylbis (2-(diphenylphosphino) ethyl) amine, sec-Butylbis (2-(dicyclohexylphosphino) ethyl) amine, and (alpha-Methylbenzyl) bis (2-(dicyclohexylphosphino) ethyl) amine and Their Organom
Bianchini C, et al.
Organometallics, 16(20), 4403-4414 (1997)
Stereospecific synthesis of secondary amines by the Mitsunobu reaction
Edwards ML, et al.
Tetrahedron Letters, 31(24), 3417-3420 (1990)
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