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质量水平
方案
98%
表单
liquid
旋光性
[α]/D +1.0 to −1.0°
折射率
n20/D 1.450 (lit.)
沸点
173-176 °C (lit.)
密度
0.943 g/mL at 25 °C (lit.)
官能团
amine
hydroxyl
SMILES字符串
CC(N)CO
InChI
1S/C3H9NO/c1-3(4)2-5/h3,5H,2,4H2,1H3
InChI key
BKMMTJMQCTUHRP-UHFFFAOYSA-N
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应用
DL-Alaninol has been used in the synthesis of:
- N6-α-(I-hydroxypropyl) lysine
- diastereomers of DL-β-amino alcohols
- enantiopure and racemic samples of 2-methyl-N-tosylaziridine
- (±)-3-(5-dimethylcarbamoyl-pent-1-enyl)-N-(2-hydroxy-1-methyl-ethyl)benzamide
警示用语：
Danger
危险声明
危险分类
Skin Corr. 1B
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 3
闪点(°F)
183.2 °F - closed cup
闪点(°C)
84 °C - closed cup
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
P M Hoi et al.
British journal of pharmacology, 152(5), 751-764 (2007-09-25)
A putative novel cannabinoid receptor mediates vasorelaxation to anandamide and abnormal-cannabidiol and is blocked by O-1918 and by high concentrations of rimonabant. This study investigates VSN16, a novel water-soluble agonist, as a vasorelaxant potentially acting at non-CB1, non-CB2 cannabinoid receptors
Ian C Stewart et al.
Journal of the American Chemical Society, 127(50), 17616-17617 (2005-12-15)
Sulfonylaziridines have been identified as excellent monomers for living ring-opening polymerization initiated by nucleophilic sulfonylamides. The resulting polymers exhibit low polydispersities and controllable molecular weights. The enantiopurity of the monomer plays a key role: racemic samples yield soluble polymers of
The role of lysine residues in the activity of 2-keto-3-deoxy-6-phosphogluconate aldolase.
J M Ingram et al.
The Journal of biological chemistry, 240(11), 4146-4151 (1965-11-01)
The substrate-dependent steric course of the ethanolamine ammonia-lyase reaction.
P Diziol et al.
European journal of biochemistry, 106(1), 211-224 (1980-05-01)
Julien Pytkowicz et al.
Organic & biomolecular chemistry, 8(20), 4540-4542 (2010-09-08)
Two efficient routes are reported for the synthesis of both enantiomers of trifluoroalaninol in enantiopure form. The first pathway involves a Strecker-type reaction performed from a chiral trifluoromethyloxazolidine (Fox). The second route, which is more direct, involves, as a key
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