135906-03-5

135906-03-5 - Names and Identifiers

Name	Endo-3-amine-9-methyl-9-azabicyclo[3,3,1]nonane dihydrochloride
Synonyms	9-Methyl-9-azobicyclo[3.3.1]nonane-3-AMINE.2HCL Endo-9-methyl-9-azabicyclo[3,3,1]nonan-3-amine 2HCl ENDO-3-AMINE -9-METHYL-9-AZABICYCLO3,3,1NONANE 2HCL Endo-3-amine-9-methyl-9-azabicyclo[3,3,1]nonane DiHCl endo-9-Methyl-9-azabicyclo[3.3.1]nonan-3-aMine Dihydrochloride Endo-3-amino-9-methyl-9-azabicyclo[3,3,1]nonanedihydrochloride Endo-3-amine-9-methyl-9-azabicyclo[3,3,1]nonane dihydrochloride Endo-3-Amine -9-Methyl-9-Azabicyclo[3,3,1]Nonane Dihydrochloride rel-(1R,3r,5S)-9-Methyl-9-azabicyclo[3.3.1]nonan-3-amine dihydrochloride
CAS	135906-03-5
EINECS	1592732-453-0

135906-03-5 - Physico-chemical Properties

Molecular Formula	C9H18N2.2ClH
Molar Mass	227.177
Boling Point	294.6℃ at 760mmHg
Storage Condition	Inert atmosphere,Room Temperature
MDL	MFCD09750974

135906-03-5 - Introduction

Endo-9-methyl-9-azabicyclo [3,3,1] nonan-3-amine hydrochloride (N-methyl-9-azabicyclo[3.3.1]nonane-3-amine hydrochloride) is an organic compound. The following is a description of its nature, use, preparation and safety information:

1. nature:
-Appearance: White crystalline powder
-Molecular formula: C10H22N2 · HCl
-Molecular weight: 208.76g/mol
-melting point: about 179-183 ℃
-Solubility: Soluble in water and alcohol solvents.

2. use:
-Intra -9-methyl -9-azabicyclo [3,3,1] nonan-3-amine hydrochloride has certain applications in the field of medicine. It can be used as a pharmaceutical intermediate for the synthesis of antidepressants, muscle relaxants and other drugs.
-The compound is also used in organic synthesis reactions, such as as catalysts, raw materials or reducing agents.

3. Preparation method:
Intra -9-methyl -9-azabicyclo [3,3,1] nonan-3-amine hydrochloride can be synthesized by the following synthetic route:
-First, first synthesize cyclohexadiene and react with copper cyanide to obtain bicycloheptenyl copper salt.
-Then, the bicycloheptenyl copper salt is reacted with chloromethyl amine to generate bicycloheptenyl methyl amine.
-Finally, bicycloheptenylmethylamine is reacted with hydrochloric acid to obtain introdo-9-methyl-9-azabicyclo [3,3,1] nonan-3-amine hydrochloride.

4. Safety Information:
-Inward -9-methyl -9-azabicyclo [3,3,1] nonan-3-amine hydrochloride is generally relatively safe under normal use.
-Avoid contact with eyes, skin and respiratory tract when using.
-Use appropriate personal protective equipment such as lab gloves, goggles, and protective masks when using or handling compounds.
-It should be stored in a dry, cool, well-ventilated place, away from fire and combustibles.

Please note that the above information is for reference only. Please refer to the relevant literature and safety data sheets and follow proper laboratory practices when handling the compound or for practical use.

Last Update：2024-04-09 21:01:54