857335
(1S,2R)-(+)-麻黄碱 盐酸盐
99%
别名:
(1S,2R)-(+)-α-(1-甲氨基乙基)苯甲醇 盐酸盐, (1S,2R)-(+)-2-甲基氨基-1-苯基-1-丙醇 盐酸盐, D-α-(1-甲氨基乙基)苯甲醇 盐酸盐
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关于此项目
线性分子式:
C6H5CH[CH(NHCH3)CH3]OH · HCl
化学文摘社编号:
分子量:
201.69
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
EC Number:
246-090-7
Beilstein/REAXYS Number:
6118541
MDL number:
产品名称
(1S,2R)-(+)-麻黄碱 盐酸盐, 99%
InChI key
BALXUFOVQVENIU-GHXDPTCOSA-N
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
SMILES string
Cl[H].CN[C@H](C)[C@@H](O)c1ccccc1
assay
99%
form
crystals
optical activity
[α]23/D +34.3°, c = 5 in H2O
mp
218-220 °C (lit.)
Quality Level
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Application
(1S,2R)-(+)-Ephedrine hydrochloride may be used in the preparation of (R)-methcathinone via permanganate method of oxidation.
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.
Efficient synthesis of cis-thiazolidinethiones derived from ephedrines
Cruz A, et al.
Tetrahedron Asymmetry, 22(4), 394-398 (2011)
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)
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)
An efficient synthesis of aziridines from ephedrines
Cruz A, et al.
Tetrahedron Asymmetry, 21(8), 909-913 (2010)
Noel Kong et al.
Journal of separation science, 37(21), 3015-3023 (2014-08-22)
A sensitive hydrophilic interaction liquid chromatography coupled with tandem mass spectrometry method was developed and validated for the simultaneous detection and quantification of etilefrine and oxilofrine in equine blood plasma and urine. The method is highly sensitive and specific with
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