Detail of "1485-15-0"

CAS Number:
1485-15-0
Name:
Benzenemethanol, a-[(1S)-1-aminoethyl]-,hydrochloride (1:1), (aS)-rel-
Molecular Structure:
Formula:
C9H13 N O . Cl H
Molecular Weight:
189.6824
Synonyms:
Benzenemethanol,a-(1-aminoethyl)-, hydrochloride,(R*,R*)-(?à)-; Benzenemethanol, a-[(1R)-1-aminoethyl]-,hydrochloride, (aR)-rel-(9CI); Norpseudoephedrine, hydrochloride, (?à)- (8CI); (?à)-threo-2-Amino-1-phenyl-1-propanol hydrochloride;Benzenemethanol, a-(1-aminoethyl)-,hydrochloride, (R*,R*)-; Pseudonorephedrine hydrochloride; threo-Norpseudoephedrinehydrochloride
Density:
g/cm³
Boiling Point:
264.2°Cat760mmHg
Flash Point:
113.6°C

Please post your buying leads,so that our qualified suppliers will soon contact you!
*Required Fields

Stereoselectivity of 9,9'-spirobifluorene crown ethers towards a-amino alcohols: Stereoselectivity of 9,9'-spirobifluorene crown ethers towards a-amino alcohols. Prelog, Vladimir; Mutak, Stjepan (Lab. Org. Chem. 1485-15-0 and 37577-07-4 are also occured in this study., Eidg. Tech. Hochsch. Zurich, Zurich CH-8092, Switz.). Helv. Chim. Acta, 66(7), 2274-8 (German) 1983. CODEN: HCACAV. ISSN: 0018-019X. DOCUMENT TYPE: Journal CA Section: 22 (Physical Organic Chemistry) Crown ethers I (n = 1, 2, 3), II, III, and IV were tested by partition expts. for their stereoselectivity toward RCH(OH)CH(NHR1)R2 (R, R2 = H, Me, Ph; R1 = H, Me), and several generalizations were made. For example, the hosts with an R or R,R configuration preferred, with few exceptions, guests with an R configuration next to the N atom. .

Enantioselective pharmacokinetics of phenylpropanolamine in dogs: Enantioselective pharmacokinetics of phenylpropanolamine in dogs. Schneider, M.; Woehrle, F.; Boisrame, B. (Vetoquinol R & D Department, Lure, Fr.).Several reagents with their cas registry numbers 154-41-6 and 1485-15-0 are used here. Journal of Veterinary Pharmacology and Therapeutics, 26(Suppl. 1), 103 (English) 2003 Blackwell Publishing Ltd. CODEN: JVPTD9. ISSN: 0140-7783. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacology) Enantioselective pharmacokinetics of phenylpropanolamine was studied in dogs after i.v. and oral administration of Propalin. The results showed that the l-enantiomer was eliminated more slower than the d-enantiomer. This finding may be explained by the much more stronger binding of l-phenylpropanolamine to the a1 receptors. .