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24426-40-2

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24426-40-2 Usage

Description

(Ethylamino)acetonitrile, with the molecular formula C4H8N2, is a chemical compound that features a carbon-nitrogen triple bond, known as a nitrile, and an ethylamino group, which is an ethyl group attached to an amino group. This versatile compound serves as a crucial intermediate in the synthesis of various organic compounds and pharmaceuticals, and it also finds use in the production of agrochemicals and pigments, making it a valuable asset in the chemical and pharmaceutical industries.

Uses

Used in Pharmaceutical Industry:
(Ethylamino)acetonitrile is used as an intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and medications. Its unique structure allows for the creation of a wide range of therapeutic compounds.
Used in Chemical Industry:
In the chemical industry, (ethylamino)acetonitrile is utilized as a building block in the production of agrochemicals, which are essential for enhancing crop protection and yield. Its incorporation in the synthesis process aids in the development of more effective and targeted agrochemical products.
Used in Pigment Production:
(Ethylamino)acetonitrile also finds application in the manufacturing of pigments, which are used in various industries such as cosmetics, paints, and plastics. Its role in pigment synthesis allows for the creation of a diverse array of colors and properties, catering to the specific needs of different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 24426-40-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,2 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 24426-40:
(7*2)+(6*4)+(5*4)+(4*2)+(3*6)+(2*4)+(1*0)=92
92 % 10 = 2
So 24426-40-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H8N2/c1-2-6-4-3-5/h6H,2,4H2,1H3

24426-40-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(ethylamino)acetonitrile

1.2 Other means of identification

Product number -
Other names Acetonitrile, (ethylamino)-

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:24426-40-2 SDS

24426-40-2Relevant articles and documents

Bleach and oxidation catalyst

-

, (2008/06/13)

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

Cignarella, G.,Villa, S.,Barlocco, D.

, p. 115 - 120 (2007/10/02)

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

Ha,Nam,Park

, p. 155 - 160 (2007/10/02)

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.

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