1126-67-6

Basic information

• Product Name: hexahydro-2H-azocine-1-ethylamine
• Synonyms: hexahydro-2H-azocine-1-ethylamine;N-(BETA-AMINOETHYL)AZACYCLOOCTANE;N-(B-AMINOETHYL)AZACYCLOOCTANE;3,4,5,6,7,8-Hexahydro-1(2H)-azocineethanamine;Octahydroazocine-1-ethanamine;2-(azocan-1-yl)ethanamine;2-(azocan-1-yl)ethylamine;2-(octahydro-1-azocinyl)-ethylamine
• CAS NO: 1126-67-6
• Molecular Formula: C₉H₂₀N₂
• Molecular Weight: 156.2685
• EINECS: 214-423-5
• Mol File: 1126-67-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 232.9°Cat760mmHg
• Flash Point: 88.6°C
• Appearance: /
• Density: 0.896g/cm³
• Vapor Pressure: 0.0576mmHg at 25°C
• Refractive Index: 1.471
• CAS DataBase Reference: hexahydro-2H-azocine-1-ethylamine(CAS DataBase Reference)
• NIST Chemistry Reference: hexahydro-2H-azocine-1-ethylamine(1126-67-6)
• EPA Substance Registry System: hexahydro-2H-azocine-1-ethylamine(1126-67-6)

Safety Data

• Hazardous Substances Data: 1126-67-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H20N2/c10-6-9-11-7-4-2-1-3-5-8-11/h1-10H2

Upstream product

• 1121-92-2 heptamethyleneimine 
• 84803-55-4 azocan-1-yl-acetonitrile 

Downstream Products

• 55-65-2 guanethidine 

Relevant articles and documents

A NEW GROUP OF ANTIFIBRILLANTS. N-(OMEGA-AMINOALKYL)PHTHALIMIDES.

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N-Hydroxyl derivatives of guanidine based drugs as enzymatic NO donors

Recent research suggests that NO may play a role in the physiological effects of some guanidine-containing drugs. In this report, three guanidine-containing drugs (guanadrel, guanoxan, and guanethidine) together with their N-hydroxyl derivatives were synthesized and their NO-releasing abilities catalyzed by nitric oxide synthases (NOSs) and horseradish peroxidase were evaluated. The guanidine containing compounds could not release NO in the presence of NOS or peroxidase. The corresponding N-hydroxyl compounds exhibited weak NO-releasing ability under the catalyzed of NOS and good NO-releasing ability under the oxidation by horseradish peroxidase in the presence of H2O2. These compounds also displayed vasodilatory activity. Elsevier Science Ltd. All rights reserved.