24426-40-2

Basic information

• Product Name: (ethylamino)acetonitrile
• Synonyms: (ethylamino)acetonitrile;Acetonitrile, (ethylamino)-;Acetonitrile, 2-(ethylamino)-;Einecs 246-243-8
• CAS NO: 24426-40-2
• Molecular Formula: C₄H₈N₂
• Molecular Weight: 84.11972
• EINECS: 246-243-8
• Mol File: 24426-40-2.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 227°Cat760mmHg
• Flash Point: 91.1°C
• Appearance: /
• Density: 0.883g/cm³
• Vapor Pressure: 1.69mmHg at 25°C
• Refractive Index: 1.412
• PKA: 4.77±0.10(Predicted)
• CAS DataBase Reference: (ethylamino)acetonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: (ethylamino)acetonitrile(24426-40-2)
• EPA Substance Registry System: (ethylamino)acetonitrile(24426-40-2)

Safety Data

• Hazardous Substances Data: 24426-40-2(Hazardous Substances Data)

Usage

General Description

(Ethylamino)acetonitrile is a chemical compound with the molecular formula C4H8N2. It is a nitrile, meaning it contains a carbon-nitrogen triple bond, and it also contains an ethylamino group, which consists of an ethyl group bonded to an amino group. (ethylamino)acetonitrile is often used as an intermediate in the synthesis of other organic compounds and pharmaceuticals. It can also be utilized as a building block in the production of agrochemicals and pigments. (Ethylamino)acetonitrile is a versatile compound with a range of potential applications in the chemical and pharmaceutical industries.

InChI:InChI=1/C4H8N2/c1-2-6-4-3-5/h6H,2,4H2,1H3

Upstream product

• 50-00-0 formaldehyd 
• 75-04-7 ethylamine 
• 107-16-4 glycolonitrile 
• 506-68-3 bromocyane 
• 3010-02-4 diethylaminoacetonitrile 
• 151-50-8 potassium cyanide 
• 7779-27-3 1,3,5-triethyl-1,3,5-triazacyclohexane 
• 7677-24-9 trimethylsilyl cyanide 
• 544-92-3 copper(I) cyanide 
• 557-66-4 ethanamine hydrochloride 
• 108-88-3 toluene 

Downstream Products

• 110-72-5 N-ethylethane-1,2-diamine 
• 22977-88-4 2-Chloro-N-cyanomethyl-N-ethyl-4-nitro-benzamide 
• 22978-15-0 N-Cyanomethyl-N-ethyl-3,5-dinitro-benzamide 
• 22978-19-4 2,5-Dichloro-N-cyanomethyl-N-ethyl-3-nitro-benzamide 
• 22985-08-6 2,4-Dichloro-N-cyanomethyl-N-ethyl-3,5-dinitro-benzamide 
• 22977-86-2 N-(4-Amino-3,5-dichlorbenzoyl)-N-ethylcyanamid 
• 22985-11-1 N-Cyanomethyl-N-ethyl-2-methyl-3,5-dinitro-benzamide 
• 22978-22-9 4-Chloro-N-cyanomethyl-N-ethyl-3,5-dinitro-benzamide 
• 22985-06-4 2-Chloro-N-cyanomethyl-N-ethyl-3,5-dinitro-benzamide 

Relevant articles and documents

Bleach and oxidation catalyst

A bleach and oxidation catalyst is provided comprising a catalytically active iron, manganese or copper complex including a specified pentadentate nitrogen-containing ligand. The metal complex can activate hydrogen peroxide or peroxyacids and provides favourable stain removal properties. In addition, a considerably improved stability of these metal complex compounds in alkaline aqueous environment has been obtained, in particular at the peroxy compound concentrations generally present in the fabric washing liquor.

Synthesis of a new series of 2,7-diazaspirononan-1-ones and study of their cholinergic properties

A new series of substituted 2,7-diazaspirononan-1-ones (1a-l), structurally related to the muscarinic agonist RS-86, has been synthesized and tested for cholinergic properties both in vitro and in vivo.None of the compounds showed significant cholinergic properties at either the central or peripheral level.A possible explanation for the lack of activity is given.Alzheimer's disease / cholinergic system / RS-86 / muscarinic agonists

TiCl4 induced N-methyleneamine equivalents: A new route to aminoacetonitriles

TiCl4 induced N-methyleneamine equivalents from hexahydro-1,3,5-triazines or N-(methoxymethyl)amines were reacted with trimethylsilyl cyanide to give aminoacetonitriles in 40-90% yield.