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About This Item
Empirical Formula (Hill Notation):
C9H13NO
CAS Number:
Molecular Weight:
151.21
PubChem Substance ID:
UNSPSC Code:
12352000
NACRES:
NA.22
EC Number:
207-755-7
MDL number:
Beilstein/REAXYS Number:
2207678
SMILES string
C[C@H](N)[C@H](O)c1ccccc1
grade
purum
assay
≥98.0% (NT)
optical activity
[α]20/D −41.0±1°, c = 7% in 1 M HCl
storage temp.
2-8°C
Gene Information
rat ... Adra1a(29412), Adra1b(24173), Adra1d(29413)
Regulatory Information
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Hyeon-Kyu Lee et al.
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Each of the enantiomers of both norephedrine and norpseudoephedrine were stereoselectively prepared from the common, prochiral cyclic sulfamidate imine of racemic 1-hydroxy-1-phenyl-propan-2-one by employing asymmetric transfer hydrogenation (ATH) catalyzed by the well-defined chiral Rh-complexes, (S,S)- or (R,R)-Cp*RhCl(TsDPEN), and HCO(2)H/Et(3)N as
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Here we contrast the vascular smooth muscle contractility produced by D-nor-pseudoephedrine, alone or combined with triiodothyronine, on the aorta and coronary vasculature of the rat. At high concentrations (greater than those found in normal therapeutic dosing) D-nor-pseudoephedrine contracted the aorta.
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Journal of AOAC International, 87(5), 1058-1062 (2004-10-21)
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