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5661-71-2 Usage

General Description

OCTAMETHYLENEIMINE, also known as 1,8-Octanediamine, is a chemical compound with the molecular formula C8H18N2. It is a colorless, viscous liquid with a strong amine odor. OCTAMETHYLENEIMINE is an important intermediate in the production of nylon-8 and other polymers. It is also used as a corrosion inhibitor and as a precursor for the synthesis of various organic compounds. Additionally, OCTAMETHYLENEIMINE has applications in the pharmaceutical and agricultural industries. However, it should be handled with caution as it is a skin and eye irritant, and prolonged exposure may cause respiratory irritation.

Check Digit Verification of cas no

The CAS Registry Mumber 5661-71-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,6 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5661-71:
(6*5)+(5*6)+(4*6)+(3*1)+(2*7)+(1*1)=102
102 % 10 = 2
So 5661-71-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H17N/c1-2-4-6-8-9-7-5-3-1/h9H,1-8H2

5661-71-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Octamethyleneimine

1.2 Other means of identification

Product number -
Other names 1H-Azonine, octahydro-

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:5661-71-2 SDS

5661-71-2Related news

OCTAMETHYLENEIMINE (cas 5661-71-2) in the Mannich reaction I Substituted β-amino ketones and substituted α-amino alcohols07/16/2019

A group of Mannich bases, utilizing octamethyleneimine as the amine component, has been prepared. Their preparation and biological activities are given.detailed

5661-71-2Relevant articles and documents

Expedient synthesis of N-fused indoles: A C-F activation and C-H insertion approach

Fuchibe, Kohei,Kaneko, Tsukasa,Mori, Keiji,Akiyama, Takahiko

supporting information; experimental part, p. 8070 - 8073 (2010/02/27)

Easy does it: A wide range of N-fused indole skeletons, which are core structures of many biologically potent molecules, are successfully furnished by a niobiumcatalyzed C(sp3)-H insertion reaction (see picture). The precursors are readily prepared by a palladium-catalyzed amination reaction of bromotrifluorotoluenes with cyclic amines.

BENZODIAZEPINE DERIVATIVES AND THEIR USE AS ANTAGONISTS OF CHOLECYSTOKININ AND/OR GASTRIN RECEPTORS

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, (2008/06/13)

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