2447-87-2

Basic information

• Product Name: 4-Chloro-N,N-di-n-propylbenzaMide, 97%
• Synonyms: 4-Chloro-N,N-di-n-propylbenzaMide, 97%;NSC 6038;4-chloro-N,N-dipropylbenzamide
• CAS NO: 2447-87-2
• Molecular Formula: C13H18ClNO
• Molecular Weight: 239.74112
• Mol File: 2447-87-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 359.6°Cat760mmHg
• Flash Point: 171.3°C
• Appearance: /
• Density: 1.076g/cm³
• Vapor Pressure: 2.36E-05mmHg at 25°C
• Refractive Index: 1.523
• PKA: -1.42±0.70(Predicted)
• CAS DataBase Reference: 4-Chloro-N,N-di-n-propylbenzaMide, 97%(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Chloro-N,N-di-n-propylbenzaMide, 97%(2447-87-2)
• EPA Substance Registry System: 4-Chloro-N,N-di-n-propylbenzaMide, 97%(2447-87-2)

Safety Data

• Hazardous Substances Data: 2447-87-2(Hazardous Substances Data)

Usage

General Description

4-Chloro-N,N-di-n-propylbenzamide, 97% is a chemical compound with a molecular formula C14H20ClNO. It is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. The 97% purity of this compound makes it suitable for use in various chemical processes and reactions, ensuring high quality and consistent results. This chemical is known for its role as a building block in the production of organic compounds and is often used as a reagent in laboratories and industrial settings. It is important to handle this chemical 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

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

Relevant articles and documents

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.