192171
DL-Alaninol
98%
Sinónimos:
(±)-2-Amino-1-propanol
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Fórmula lineal:
CH3CH(NH2)CH2OH
Número CAS:
Peso molecular:
75.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
228-207-3
Beilstein/REAXYS Number:
1209234
MDL number:
Assay:
98%
Form:
liquid
Servicio técnico
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Permítanos ayudarleQuality Level
assay
98%
form
liquid
optical activity
[α]/D +1.0 to −1.0°
refractive index
n20/D 1.450 (lit.)
bp
173-176 °C (lit.)
density
0.943 g/mL at 25 °C (lit.)
functional group
amine, hydroxyl
SMILES string
CC(N)CO
InChI
1S/C3H9NO/c1-3(4)2-5/h3,5H,2,4H2,1H3
InChI key
BKMMTJMQCTUHRP-UHFFFAOYSA-N
Application
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
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Clase de almacenamiento
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
183.2 °F - closed cup
flash_point_c
84 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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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
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
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)