14256-69-0

Basic information

• Product Name: N*1*-Cyclohexyl-N*1*-methyl-ethane-1,2-diamine
• Synonyms: N*1*-Cyclohexyl-N*1*-methyl-ethane-1,2-diamine;N1-cyclohexyl-N1-Methyl-1,2-EthanediaMine;N'-cyclohexyl-N'-methylethane-1,2-diamine
• CAS NO: 14256-69-0
• Molecular Formula: C₉H₂₀N₂
• Molecular Weight: 156.2685
• Mol File: 14256-69-0.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: N*1*-Cyclohexyl-N*1*-methyl-ethane-1,2-diamine(CAS DataBase Reference)
• NIST Chemistry Reference: N*1*-Cyclohexyl-N*1*-methyl-ethane-1,2-diamine(14256-69-0)
• EPA Substance Registry System: N*1*-Cyclohexyl-N*1*-methyl-ethane-1,2-diamine(14256-69-0)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 14256-69-0(Hazardous Substances Data)

Usage

General Description

N-cyclohexyl-N-methyl-ethane-1,2-diamine is a chemical compound used primarily as a ligand in coordination chemistry and as an intermediate in the synthesis of pharmaceuticals. It is a diamine compound, meaning it contains two amino groups, and is commonly referred to as CHEME, for short. It is a colorless liquid with a characteristic amine odor and is moderately soluble in water. CHEME has been studied for its potential use in the treatment of neurological disorders and as a chelating agent for metal ions in various industrial applications. However, it is important to handle CHEME with care, as it is considered a hazardous chemical and can cause irritation upon contact with the skin or eyes.

Upstream product

• 96517-08-7 2-(cyclohexyl(methyl)amino)acetonitrile 
• 3638-64-0 1-nitroethylene 
• 100-60-7 N-methylcyclohexylamine 
• 574-98-1 2-(2-bromoethyl)isoindoline-1,3-dione 

Downstream Products

• 40432-71-1 <2-(Cyclohexyl-methyl-amino)-aethyl>-guanidin 
• 91336-71-9 N-Methyl-N-cyclohexyl-N'-<2-hydroxy-aethyl>-aethylendiamin 

Relevant articles and documents

N-(amino)alkyl)-1-pyrrolidine, 1-piperidine and 1-homopiperidinecarboxamides (and thiocarboxamides) with sulfur linked substitution in the 2, 3 or 4-positions

Novel pyrrolidine, piperidine and homopiperidinecarboxamide and thiocarboxamide compounds having the formula: STR1 wherein X is --S--, --S(O)-- or --S(O)2 --; A is a loweralkalene chain and A1 and A2 are alkalene chains when p and d are one; R, R1 and R2 are hydrogen, loweralkyl, phenyl cycloalkyl or phenylalkyl and R1 and R2 may form a heterocyclic residue with the adjacent nitrogen atom; Q is a selected aromatic radical, and the pharmaceutically acceptable acid addition salts useful as cardiac antiarrhythmia agents are disclosed. Novel chemical intermediates, unsubstituted on pyrrolidine, piperidine and homopiperidine nitrogen but with --(A2)p --X--(A2)d --Q side chain are also disclosed.

Pharmacologic action of new derivatives chemically related to guanethidine

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