132527
(S)-(+)-2-Amino-1-butanol
≥98%
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About This Item
Linear Formula:
C2H5CH(NH2)CH2OH
CAS Number:
Molecular Weight:
89.14
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
EC Number:
227-475-9
Beilstein/REAXYS Number:
1718930
MDL number:
Assay:
≥98%
Form:
liquid
Quality Level
assay
≥98%
form
liquid
optical activity
[α]20/D +10°, neat
optical purity
ee: 96% (GLC)
refractive index
n20/D 1.4521 (lit.)
bp
172-174 °C (lit.)
density
0.944 g/mL at 25 °C (lit.)
functional group
amine, hydroxyl
SMILES string
CC[C@H](N)CO
InChI
1S/C4H11NO/c1-2-4(5)3-6/h4,6H,2-3,5H2,1H3/t4-/m0/s1
InChI key
JCBPETKZIGVZRE-BYPYZUCNSA-N
Application
(S)-(+)-2-Amino-1-butanol is a chiral amino alcohol that may be used in the synthesis of (S)-2-(6-benzylamino-9-isopropyl-9H-purin-2-ylamino) butan-1-ol, an (S)-enantiomer of roscovitine. It can also be used to synthesize homochiral 2-methylpyrroles. (S)-(+)-2-Amino-1-butanol is an intermediate for the synthesis of (S,S)-ethambutol, an antibacterial agent for treating tuberculosis.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
203.0 °F - closed cup
flash_point_c
95 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Synthesis and photooxygenation of homochiral 2-methylpyrrole derivatives of chiral amino alcohols: simple, selective access to chiral bicyclic lactams
Aydogan F and Demir AS
Tetrahedron Asymmetry, 15(2), 259-265 (2004)
Enantioselective synthesis of (S, S)-ethambutol using proline-catalyzed asymmetric a-aminooxylation and a-amination
Kotkar SP and Sudalai A
Tetrahedron Asymmetry, 17(11), 1738-1742 (2006)
Synthesis and configuration of the cyclin-dependent kinase inhibitor roscovitine and its enantiomer.
Wang S, et al
Tetrahedron Asymmetry, 12(20), 2891-2894 (2001)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 132527-5G | 04061838729026 |
| 132527-1G | 04061837638817 |