857335
(1S,2R)-(+)-Ephedrine hydrochloride
99%
Synonym(s):
(1S,2R)-(+)-α-(1-Methylaminoethyl)benzyl alcohol hydrochloride, (1S,2R)-(+)-2-Methylamino-1-phenyl-1-propanol hydrochloride, D-α-(1-Methylaminoethyl)benzyl alcohol hydrochloride
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About This Item
Linear Formula:
C6H5CH[CH(NHCH3)CH3]OH · HCl
CAS Number:
Molecular Weight:
201.69
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
EC Number:
246-090-7
Beilstein/REAXYS Number:
6118541
MDL number:
assay
99%
form
crystals
optical activity
[α]23/D +34.3°, c = 5 in H2O
mp
218-220 °C (lit.)
SMILES string
Cl[H].CN[C@H](C)[C@@H](O)c1ccccc1
InChI
1S/C10H15NO.ClH/c1-8(11-2)10(12)9-6-4-3-5-7-9;/h3-8,10-12H,1-2H3;1H/t8-,10-;/m1./s1
InChI key
BALXUFOVQVENIU-GHXDPTCOSA-N
General description
Ephedrines are quite significant components in asymmetric synthesis; they are commonly used as key components in the preparation of heterocyclic compounds. They are also used as reagents/ catalytic substances or ligands for the synthesis of aryl/heteroaryl derivatives and organometallic complexes.
Application
(1S,2R)-(+)-Ephedrine hydrochloride may be used in the preparation of (R)-methcathinone via permanganate method of oxidation.
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Find documentation for the products that you have recently purchased in the Document Library.
An efficient synthesis of aziridines from ephedrines
Cruz A, et al.
Tetrahedron Asymmetry, 21(8), 909-913 (2010)
Metal-Drug Interactions: Synthesis and Spectroscopic Characteristics, Surface Morphology, and Pharmacological Activity of Ephedrine-HCl Complexes with Mo (V), Nb (V), Ga (III), and Ge (IV)
El-Habeeb AA and Refat MS
Russ. J. Gen. Chem., 88(10), 2163-2169 (2018)
Chiral identification and determination of ephedrine, pseudoephedrine, methamphetamine and metecathinone by gas chromatography and nuclear magnetic resonance.
LeBelle MJ, et al.
Forensic Science International, 71(3), 215-223 (1995)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 857335-25G | 04061833483930 |