Hyoscyamine | |
---|---|
Molecular structure via molpic based on CDK |
Physical properties [] | |
---|---|
Molecular mass | 289.4 g/mol [1] |
Appearance | SILKY, TETRAGONAL NEEDLES FROM EVAPORATING ALCOHOL [1] |
Melting point | 108.5 °C [1] |
Solubility | 1 G DISSOLVES IN 281 ML OF WATER (PH 9.5), 69 ML OF ETHER, 150 ML OF BENZENE, 1 ML OF CHLOROFORM; FREELY SOL IN ALCOHOL, DIL ACIDS [1] |
Predicted LogP | 1.8 [1] |
Structural Identifiers [] | |
---|---|
Molecular formula | C17H23NO3 [1] |
IUPAC name | [(1S,5R)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] (2S)-3-hydroxy-2-phenylpropanoate [1] |
SMILES | CN1[C@@H]2CC[C@H]1CC(C2)OC(=O)[C@H](CO)C3=CC=CC=C3 [1] |
InChI | InChI=1S/C17H23NO3/c1-18-13-7-8-14(18)10-15(9-13)21-17(20)16(11-19)12-5-3-2-4-6-12/h2-6,13-16,19H,7-11H2,1H3/t13-,14+,15?,16-/m1/s1 [1] |
InChIKey | RKUNBYITZUJHSG-VFSICIBPSA-N [1] |
Hyoscyamine
Hyoscyamine (also known as L-Hyoscyamine, Daturine, (-)-Hyoscyamine, Duboisine, (-)-Atropine, L-Tropine tropate, (S)-(-)-Hyoscyamine, Cystospaz, l-Atropine or (S)-Atropine) is a
Chemistry
Salts []
Hyoscyamine is typically found in the form of its hydrochloride and sulfate salts.
Stereochemistry []
Hyoscyamine is a absolute mixture