280-05-7

Basic information

• Product Name: pseudohyoscyamine
• Synonyms: norhyoscyamine;pseudohyoscyamine;nortropane;8-Azabicyclo[3.2.1]octane;8-azabicyclo[3.2.1]octane hydrochloride
• CAS NO: 280-05-7
• Molecular Formula: C₇H₁₃N
• Molecular Weight: 111.18
• Mol File: 280-05-7.mol
• Article Data: 10

Chemical Properties

• Melting Point: 307-309 °C
• Boiling Point: 169.9°C at 760 mmHg
• Flash Point: 48.2°C
• Appearance: /
• Density: 0.934g/cm³
• Vapor Pressure: 1.5mmHg at 25°C
• Refractive Index: 1.478
• Storage Temp.: 2-8°C
• PKA: pKa 10.28(H2O,t =21±2,Iundefined) (Uncertain)
• CAS DataBase Reference: pseudohyoscyamine(CAS DataBase Reference)
• NIST Chemistry Reference: pseudohyoscyamine(280-05-7)
• EPA Substance Registry System: pseudohyoscyamine(280-05-7)

Safety Data

• Hazardous Substances Data: 280-05-7(Hazardous Substances Data)

Usage

Uses

8-Azabicyclo[3.2.1]octane is used as a reactant in the preparation of enantiomerically pure 8-azabicyclo[3.2.1]octane derivatives.

InChI:InChI=1/C7H13N/c1-2-6-4-5-7(3-1)8-6/h6-8H,1-5H2

Upstream product

• 1005389-51-4 C₉H₁₅NO₂ 
• 529-17-9 tropane 
• 50893-53-3 carbonochloridic acid 1-chloro-ethyl ester 
• 113340-10-6 trans-1-(benzylamino)-4-chlorocycloheptane HCl 
• 95687-88-0 N-benzoyl-8-oxa-9-azabicyclo<3.2.2>non-6-ene 
• 95687-90-4 cis-4-(benzoylamino)-2-cycloheptenol 
• 95687-91-5 cis-4-(benzoylamino)cycloheptanol 
• 146309-04-8 6-Oxa-7-aza-bicyclo[3.2.2]non-8-ene-7-carboxylic acid benzyl ester 
• 113340-09-3 cis-4-(benzylamino)cycloheptanol 
• 113340-06-0 8-oxa-9-azabicyclo<3.2.2>non-6-ene 
• 113340-18-4 cis-4-aminocyclohept-2-enol 
• 876938-53-3 Cyclohepta-1,3-diene 
• 10034-85-2 hydrogen iodide 
• 538-09-0 nortropine 

Downstream Products

• 74327-95-0 N-chloronortropane 
• 41851-67-6 N-hydroxynortropane 
• 38824-17-8 8-azabicyclo[3.2.1]octane-N-oxyl 
• 90949-55-6 2-nortropan-8-yl-ethanol 
• 1621168-72-6 {(S)-6-[(R)-4-(8-azabicyclo[3.2.1]oct-8-ylmethyl)-5-trifluoromethylindan-1-yloxy]-2,3-dihydrobenzofuran-3-yl}acetic acid methyl ester 

Relevant articles and documents

-

-

Efficient oxidation of alcohols electrochemically mediated by azabicyclo-N-oxyls

Preparation of azabicyclo-N-oxyls and the electrochemical oxidation of alcohols using them as mediators have been exploited. This oxidation was applicable to a transformation of sterically hindered secondary alcohols into the corresponding ketones in high yields.

Pyridine, pyrimidine, quinoline, quinazoline, and naphthalene urotensin-II receptor antagonists

The present invention relates to urotensin II receptor antagonists, pharmaceutical compositions containing them and their use.