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N-ethyl-N-(4-nitrobenzyl)ethanamine is an organic compound with the chemical formula C11H16N2O2. It is a derivative of ethanamine, featuring a nitrobenzyl group attached to the nitrogen atom. This yellow crystalline substance is soluble in organic solvents and has a molecular weight of 208.26 g/mol. The compound is synthesized through various chemical reactions and is used in the pharmaceutical industry as an intermediate for the production of certain drugs. It is also known for its potential applications in the synthesis of agrochemicals and other specialty chemicals. Due to its reactivity and the presence of a nitro group, it is important to handle N-ethyl-N-(4-nitrobenzyl)ethanamine with care, following proper safety protocols.

6314-55-2

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6314-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6314-55-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6314-55:
(6*6)+(5*3)+(4*1)+(3*4)+(2*5)+(1*5)=82
82 % 10 = 2
So 6314-55-2 is a valid CAS Registry Number.

6314-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethyl-N-[(4-nitrophenyl)methyl]ethanamine

1.2 Other means of identification

Product number -
Other names N,N-Diethyl-p-nitrobenzylamine

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:6314-55-2 SDS

6314-55-2Downstream Products

6314-55-2Relevant academic research and scientific papers

Aluminium complex as an efficient catalyst for the chemo-selective reduction of amides to amines

Das, Suman,Karmakar, Himadri,Bhattacharjee, Jayeeta,Panda, Tarun K.

, p. 11978 - 11984 (2019)

We report an efficient protocol for the catalytic chemo-selective reduction of tert-amides with pinacolborane (HBpin) to afford the corresponding amines in high yields using aluminium complexes [κ2-{Ph2P(X)NC9H6N}Al(Me)2] [X = S (2a), Se (2b)] as pre-catalysts at room temperature. The aluminium complexes were prepared from the reaction of [Ph2P(X)NC9H6N] [X = S (1a), Se (1b)] and trimethylaluminium in toluene. The solid-state structure of complex 2b is established. Tertiary amides with a wide array of electron-withdrawing and electron-donating functional groups were easily converted to the desired products through the selective cleavage of the amides' CO bond by aluminium hydride as an active species. A kinetic study of the catalytic reaction is also reported.

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