24676-80-0

Basic information

• Product Name: (1R,4S,5S)-3-oxa-9-azatricyclo[3.3.1.0~2,4~]non-7-yl (2S)-3-hydroxy-2-phenylpropanoate hydrochloride
• CAS NO: 24676-80-0
• Molecular Formula: C₁₆H₁₉NO₄*ClH
• Molecular Weight: 325.7873
• Mol File: 24676-80-0.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 474.7°C at 760 mmHg
• Flash Point: 240.9°C
• Vapor Pressure: 8.13E-10mmHg at 25°C
• CAS DataBase Reference: (1R,4S,5S)-3-oxa-9-azatricyclo[3.3.1.0~2,4~]non-7-yl (2S)-3-hydroxy-2-phenylpropanoate hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,4S,5S)-3-oxa-9-azatricyclo[3.3.1.0~2,4~]non-7-yl (2S)-3-hydroxy-2-phenylpropanoate hydrochloride(24676-80-0)
• EPA Substance Registry System: (1R,4S,5S)-3-oxa-9-azatricyclo[3.3.1.0~2,4~]non-7-yl (2S)-3-hydroxy-2-phenylpropanoate hydrochloride(24676-80-0)

Safety Data

• Hazardous Substances Data: 24676-80-0(Hazardous Substances Data)

Usage

Description

(1R,4S,5S)-3-oxa-9-azatricyclo[3.3.1.0~2,4~]non-7-yl (2S)-3-hydroxy-2-phenylpropanoate hydrochloride is a complex organic compound characterized by a bicyclic ring structure and a hydrochloride salt. It features a tricyclic ring system with an oxygen and nitrogen heteroatom, along with a hydroxy and phenyl functional group. This unique structure and potential pharmacological properties make it a promising candidate for pharmaceutical research and drug development.

Uses

Used in Pharmaceutical Research:
(1R,4S,5S)-3-oxa-9-azatricyclo[3.3.1.0~2,4~]non-7-yl (2S)-3-hydroxy-2-phenylpropanoate hydrochloride is used as a research compound for exploring its biological activity and potential therapeutic applications. Its unique structure and functional groups may contribute to its interaction with biological targets, making it a valuable tool in the discovery of new drugs.
Used in Drug Development:
In the pharmaceutical industry, (1R,4S,5S)-3-oxa-9-azatricyclo[3.3.1.0~2,4~]non-7-yl (2S)-3-hydroxy-2-phenylpropanoate hydrochloride is used as a starting material or intermediate in the synthesis of new drugs. Its tricyclic ring system and functional groups can be further modified to create derivatives with improved pharmacological properties, enhancing its potential as a therapeutic agent.
Used in Chemical Industry:
(1R,4S,5S)-3-oxa-9-azatricyclo[3.3.1.0~2,4~]non-7-yl (2S)-3-hydroxy-2-phenylpropanoate hydrochloride is also used in the chemical industry for various applications, such as the synthesis of other complex organic compounds or as a reagent in chemical reactions. Its hydrochloride salt form enhances its stability and solubility, making it suitable for use in a range of chemical processes.

Upstream product

• 114-49-8 hyoscine hydrobromide 

Downstream Products

• 30286-75-0 oxytropium bromide 
• 30269-62-6 (1R,2R,4S,5S,7S)-9-Allyl-9-ethyl-7-((S)-3-hydroxy-2-phenyl-propionyloxy)-3-oxa-9-azonia-tricyclo[3.3.1.0^2,4]nonane; bromide 
• 41749-07-9 (1R,2R,4S,5S,7S)-9,9-Diethyl-7-((S)-3-hydroxy-2-phenyl-propionyloxy)-3-oxa-9-azonia-tricyclo[3.3.1.0^2,4]nonane; bromide 
• 67009-40-9 (-)-N-Ethylnorscopolamin 
• 22235-93-4 (-)-N-Ethylnorscopolamin-hydrochlorid 
• 124065-43-6 (-)-N-(iminoethyl)norscopolamine 

Relevant articles and documents

The synthesis of anticholinergically active N-alkylnorscopolamines and their quaternary salts with particular consideration of the bronchospasmolytic compound (-)-N-ethylnorscopolamine methobromide (Ba 253 BR)

The synthesis of anticholinergic N-alkylnorscopolamines and their quaternary salts, especially the synthesis of (-)-N-ethylnorscopolamine methobromide (Ba 253 BR), is reported. (-)-N-Ethylnorscopolamine methobromide differs from the stereoisomeric (-)-N-ethylscopolammonium bromide not only by its physico-chemical, but also by its pharmacological properties. (-)-N-Ethylnorscopolamine methobromide represents an anticholinergic bronchodilator with long duration of action.