551996
(S)-(+)-2-Benzylamino-1-phenylethanol
97%
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About This Item
Linear Formula:
C6H5CH2NHCH2CH(OH)C6H5
CAS Number:
Molecular Weight:
227.30
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.22
Assay
97%
optical activity
[α]20/D +57°, c = 1 in chloroform
mp
115-118 °C (lit.)
functional group
amine
hydroxyl
phenyl
SMILES string
O[C@H](CNCc1ccccc1)c2ccccc2
InChI
1S/C15H17NO/c17-15(14-9-5-2-6-10-14)12-16-11-13-7-3-1-4-8-13/h1-10,15-17H,11-12H2/t15-/m1/s1
InChI key
XAOCLQUZOIZSHV-OAHLLOKOSA-N
General description
(S)-2-Benzylamino-1-phenylethanol can be used as a starting material in the preparation of iron catalysts applicable in the oxidation of secondary alcohols and benzylic methylene groups.
Application
(S)-(+)-2-Benzylamino-1-phenylethanol can be used as an intermediate in the synthesis of aziridines using α-amino and α-amido ketones via asymmetric transfer hydrogenation reaction.
Legal Information
Manufactured under license by Sterling Pharma Solutions Limited, using Jacobsen HKR technology.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Enantioselective synthesis of β-hydroxy amines and aziridines using asymmetric transfer hydrogenation of α-amino ketones
Kawamoto AM and Wills M
Journal of the Chemical Society. Perkin Transactions 1, 373(16), 1916-1928 (2001)
Enantioselective synthesis of β-hydroxy amines and aziridines using asymmetric transfer hydrogenation of α-amido ketones
Kawamoto A and Wills M
Tetrahedron Asymmetry, 11(16), 3257-3261 (2000)
Polydentate pyridyl ligands and the catalytic activity of their iron (II) complexes in oxidation reactions utilizing peroxides as the oxidants
Lenze M, et al.
J. Mol. Catal. A: Chem., 373, 161-171 (2013)
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