684414
Boc-L-alanine (2S)-2-hydroxylpropylamide
97%
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About This Item
Empirical Formula (Hill Notation):
C11H22N2O4
Molecular Weight:
246.30
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352108
MDL number:
InChI
1S/C11H22N2O4/c1-7(14)6-12-9(15)8(2)13-10(16)17-11(3,4)5/h7-8,14H,6H2,1-5H3,(H,12,15)(H,13,16)/t7-,8-/m0/s1
SMILES string
C[C@H](O)CNC(=O)[C@H](C)NC(=O)OC(C)(C)C
InChI key
QBYGMGDPOWAXSC-YUMQZZPRSA-N
assay
97%
form
solid
optical activity
[α]22/D -1.0°, c = 1 in chloroform
mp
71-80 °C
Application
Ligand for highly selective asymmetric transfer hydrogenation of prochiral ketones.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Patrik Västilä et al.
Chemical communications (Cambridge, England), (32), 4039-4041 (2005-08-11)
The direct in situ formation of highly efficient ruthenium-catalysts for the asymmetric reduction of ketones was obtained by combining chiral ligand building blocks with a ruthenium precursor.
Articles
Novel ligands enable efficient ketone reduction for chiral building block synthesis.
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