2447-87-2

Usage

Uses

Used in Pharmaceutical Industry:
4-Chloro-N,N-di-n-propylbenzamide, 97% is used as an intermediate for the synthesis of pharmaceuticals, contributing to the development of new drugs and medications.
Used in Agrochemical Industry:
4-Chloro-N,N-di-n-propylbenzamide, 97% is used as an intermediate in the production of agrochemicals, aiding in the creation of pesticides and other agricultural products.
Used in Laboratory and Industrial Settings:
4-Chloro-N,N-di-n-propylbenzamide, 97% is used as a reagent in laboratories and industrial settings, facilitating various chemical processes and reactions.
It is important to handle 4-Chloro-N,N-di-n-propylbenzamide, 97% with proper safety precautions and to use it in accordance with all relevant regulations and guidelines.

InChI:InChI=1/C13H18ClNO/c1-3-9-15(10-4-2)13(16)11-5-7-12(14)8-6-11/h5-8H,3-4,9-10H2,1-2H3

Upstream product

• 10364-95-1 1-(4-chloro-benzoyl)-1H-imidazole 
• 142-84-7 di-n-propylamine 
• 74-11-3 para-chlorobenzoic acid 
• 104-88-1 4-chlorobenzaldehyde 
• 874-59-9 4-chlorobenzoyl bromide 

Relevant academic research and scientific papers

Convenient metal-free direct oxidative amidation of aldehyde using dibromoisocyanuric acid under mild conditions

A facile method for the direct synthesis of amides from aldehydes is described. Amide bonds were synthesized by an oxidative amidation in the presence of dibromoisocyanuric acid (DBI). Treatment of aromatic and aliphatic aldehydes with dibromoisocyanuric acid generated acyl bromide intermediates, which were employed to react with a variety of secondary and primary amines to give amides. Through this reaction method, various amides were synthesized directly from aldehydes under mild conditions in high yields and short times. This facile and efficient procedure provides potential strategy for the direct synthesis of amides from aldehydes.

Activation of imidazolides using methyl trifluoromethanesulfonate: A convenient method for the preparation of hindered esters and amides

Treatment of imidazolides with methyl trifluoromethanesulfonate followed by reaction with alcohols or amines provides a convenient one-pot procedure for the preparation of esters and amides. The method is applicable to imidazolides of low reactivity as well as to hindered nucleophiles.