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Hexahydro-2H-azocine-1-ethylamine is a cyclic amine compound with the molecular formula C8H18N2. It is a derivative of azocine, a seven-membered ring containing two nitrogen atoms, and features a six-carbon saturated ring structure. The compound is characterized by the presence of a primary amine group attached to the ethylamine side chain. Hexahydro-2H-azocine-1-ethylamine is an organic compound with potential applications in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique ring structure and amine functionality.

1126-67-6

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1126-67-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1126-67-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1126-67:
(6*1)+(5*1)+(4*2)+(3*6)+(2*6)+(1*7)=56
56 % 10 = 6
So 1126-67-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H20N2/c10-6-9-11-7-4-2-1-3-5-8-11/h1-10H2

1126-67-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(azocan-1-yl)ethanamine

1.2 Other means of identification

Product number -
Other names EINECS 214-423-5

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1126-67-6 SDS

1126-67-6Downstream Products

1126-67-6Relevant academic research and scientific papers

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

Xian, Ming,Li, Xiaopeng,Tang, Xiaoping,Chen, Xinchao,Zheng, Zhongling,Galligan, James J,Kreulen, David L,Wang, Peng G

, p. 2377 - 2380 (2007/10/03)

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.

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