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Cyclohexyliminobis(acetonitrile), also known as cyclohexane-1,2-diamine bis(2-cyanoethyl) ether, is an organic compound with the chemical formula C11H16N4. It is a colorless to pale yellow liquid that is soluble in water and most organic solvents. Cyclohexyliminobis(acetonitrile) is primarily used as a corrosion inhibitor in various industrial applications, such as oil and gas pipelines, and as a stabilizer in the production of polyvinyl chloride (PVC). It is also employed as a reagent in the synthesis of other chemicals and pharmaceuticals. Due to its potential health and environmental risks, proper handling and disposal procedures are essential when working with cyclohexyliminobis(acetonitrile).

4823-13-6

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4823-13-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4823-13-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,2 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4823-13:
(6*4)+(5*8)+(4*2)+(3*3)+(2*1)+(1*3)=86
86 % 10 = 6
So 4823-13-6 is a valid CAS Registry Number.

4823-13-6SDS

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-[cyanomethyl(cyclohexyl)amino]acetonitrile

1.2 Other means of identification

Product number -
Other names ACETONITRILE,2,2'-(CYCLOHEXYLIMINO)DI

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:4823-13-6 SDS

4823-13-6Relevant academic research and scientific papers

Copper-Catalyzed three- Five- or seven-Component coupling reactions: The selective synthesis of cyanomethylamines, N,N-bis(cyanomethyl)amines and N,N'-bis(cyanomethyl)methylenediamines based on a strecker-type synthesis

Sakai, Norio,Takahashi, Nobuaki,Inoda, Daiki,Ikeda, Reiko,Konakahara, Takeo

, p. 12488 - 12499 (2013/11/06)

We have demonstrated that a cooperative catalytic system comprised of CuCl and Cu(OTf)2 could be used to effectively catalyse the three-, five- and seven-component coupling reactions of aliphatic or aromatic amines, formaldehyde, and trimethylsilyl cyanide (TMSCN), and selectively produce in good yields the corresponding cyanomethylamines, N,N-bis(cyanomethyl)amines and N,N'-bis(cyanomethyl)methylenediamines.

Preparation of N-Alkyl, 2-substituted iminodiacetic acid derivatives

Katritzky,Latif,Noble,Harris

, p. 999 - 1001 (2007/10/02)

A new method has been developed for the preparation of unsymmetrically substituted iminodiacetronitiles and iminodiacetoamides employing mild conditions and affording good overall yields.

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