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1190-79-0

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1190-79-0 Usage

Description

N-[(1E)-ethylidene]ethanamine, also known as N-ethylideneethanamine, is a primary amine with the molecular formula C4H9N. It is a colorless liquid at room temperature, characterized by a strong, ammonia-like odor. Classified as a primary amine, it contains a primary amino group and is used as a building block in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals. Due to its highly flammable nature, it requires careful handling in laboratory and industrial settings. Additionally, it is a skin and eye irritant and may have harmful effects if inhaled or ingested.

Uses

Used in Chemical Processes:
N-[(1E)-ethylidene]ethanamine is used as a chemical intermediate in various chemical processes for the synthesis of different organic compounds.
Used in Pharmaceutical Industry:
N-[(1E)-ethylidene]ethanamine is used as a building block for the synthesis of pharmaceuticals, contributing to the development of new drugs and medications.
Used in Agrochemical Industry:
N-[(1E)-ethylidene]ethanamine is used as a precursor in the production of agrochemicals, such as pesticides and herbicides, to enhance crop protection and yield.

Check Digit Verification of cas no

The CAS Registry Mumber 1190-79-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1190-79:
(6*1)+(5*1)+(4*9)+(3*0)+(2*7)+(1*9)=70
70 % 10 = 0
So 1190-79-0 is a valid CAS Registry Number.

1190-79-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethylethanimine

1.2 Other means of identification

Product number -
Other names N-ethylethylideneamine

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:1190-79-0 SDS

1190-79-0Relevant articles and documents

An alternative pathway for production of acetonitrile: Ruthenium catalysed aerobic dehydrogenation of ethylamine

Corker, Emily C.,Mentzel, Uffe V.,Mielby, Jerrik,Riisager, Anders,Fehrmann, Rasmus

, p. 928 - 933 (2013)

The oxidative synthesis of acetonitrile from ethylamine was studied using a supported ruthenium catalyst. The reaction was conducted in both batch and flow processes and high conversions (over 85%) were achieved in both cases. Selectivity of both reactions was improved by optimisation of reaction conditions, achieving over 90% selectivity in the batch process and 80% selectivity in the continuous flow process. The use of a selective solid catalyst that utilises a feedstock that can be derived from biomass, dioxygen as the oxidant and water as the solvent represents a new, green route for the independent and efficient production of acetonitrile.

Mechanistic insights into the oxidative dehydrogenation of amines to nitriles in continuous flow

Corker, Emily C.,Ruiz-Martínez, Javier,Riisager, Anders,Fehrmann, Rasmus

, p. 5008 - 5015 (2015/11/03)

The oxidative dehydrogenation of various aliphatic amines to their corresponding nitrile compounds using RuO2/Al2O3 catalysts in air was successfully applied to a continuous flow reaction. Conversions of amines (up to >99%) and yields of nitriles (up to 77%) varied depending on reaction conditions and the amine utilised. The presence of water was found to be important for the activity and stability of the RuO2/Al2O3 catalyst. The Hammett relationship and in situ infrared spectroscopy were applied to divulge details about the catalytic mechanism of the oxidative dehydrogenation of amines over RuO2/Al2O3 catalysts.

Matrix-IR spectroscopic investigations of the thermolysis and photolysis of diazoamides

Wentrup, Curt,Bibas, Herve,Kuhn, Arvid,Mitschke, Ullrich,McMills, Mark C.

, p. 10705 - 10717 (2013/11/19)

Matrix photolysis of N,N-dialkyldiazoacetamides 1a-d at 7-10 K results in either the formation of C-H insertion products (in case of N,N-dimethyl and N,N-diethyl diazoamides) or almost exclusive Wolff rearrangement to ketenes (in the case of the cyclic di

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