7461-41-8

Basic information

• Product Name: 4-Chloro-N-isopropylbenzamide
• Synonyms: 4-Chloro-N-isopropylbenzamide;p-Chloro-N-isopropylbenzamide;4-chloro-N-propan-2-ylbenzamide
• CAS NO: 7461-41-8
• Molecular Formula: C₁₀H₁₂ClNO
• Molecular Weight: 197.6614
• Mol File: 7461-41-8.mol
• Article Data: 18

Chemical Properties

• Boiling Point: 327.6°Cat760mmHg
• Flash Point: 151.9°C
• Appearance: /
• Density: 1.128g/cm³
• Vapor Pressure: 0.0002mmHg at 25°C
• Refractive Index: 1.528
• CAS DataBase Reference: 4-Chloro-N-isopropylbenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Chloro-N-isopropylbenzamide(7461-41-8)
• EPA Substance Registry System: 4-Chloro-N-isopropylbenzamide(7461-41-8)

Safety Data

• Hazardous Substances Data: 7461-41-8(Hazardous Substances Data)

Usage

General Description

4-Chloro-N-isopropylbenzamide, also known as N-(4-Chlorophenyl)-N-isopropylformamide, is a chemical compound with the molecular formula C10H12ClNO. It is a pale yellow to orange solid that is insoluble in water but soluble in organic solvents. 4-Chloro-N-isopropylbenzamide is used as an intermediate in the manufacture of pharmaceuticals and agricultural chemicals. It is also used as a raw material for the synthesis of other organic compounds. Its properties make it suitable for use in various synthetic processes, making it a valuable compound for chemical and pharmaceutical industries.

InChI:InChI=1/C10H12ClNO/c1-7(2)12-10(13)8-3-5-9(11)6-4-8/h3-7H,1-2H3,(H,12,13)

Upstream product

• 75-31-0 isopropylamine 
• 74-11-3 para-chlorobenzoic acid 
• 79606-45-4 N,N-diisopropyl 4-chlorobenzamide 
• 122-01-0 4-chloro-benzoyl chloride 
• 19172-47-5 Lawessons reagent 
• 945550-68-5 N-isopropyl-4-chlorobenzohydroxamic acid 
• 3031-21-8 bis(O,O-diisopropoxyphosphinothioyl)disulfide 
• 1144028-98-7 N-isopropyl-4-chlorobenzohydroxamic acid sodium salt 
• 598-45-8 i-propyl isocyanide 
• 673-41-6 p-chlorobenzenediazonium tetrafluoroborate 
• 106-47-8 4-chloro-aniline 
• 2700-30-3 N,N-diisorpopylformamide 
• 106-43-4 para-chlorotoluene 
• 64-18-6 formic acid 

Downstream Products

• 39887-80-4 4-chloro-N-isopropylbenzimidoyl chloride 
• 85046-79-3 C₁₂H₁₁ClN₂O₃ 
• 1126-46-1 Methyl 4-chlorobenzoate 
• 7335-27-5 ethyl 4-chlorobenzoate 
• 1433955-28-2 4-chloro-N-isopropyl-5,6,7,8-tetraphenyl-1-naphthamide 
• 27895-56-3 N-(2-propyl)-4-chlorobenzylideneamine 
• 104-88-1 4-chlorobenzaldehyde 
• 56-33-7 1,1,3,3-tetramethyl-1,3-diphenyldisiloxane 
• 18713-58-1 1-(4-chlorophenyl)-2-methylpropan-1-one 
• 3277-80-3 (4-chlorophenyl)(cyclohexyl)methanone 

Relevant articles and documents

CuO-decorated magnetite-reduced graphene oxide: a robust and promising heterogeneous catalyst for the oxidative amidation of methylarenes in waterviabenzylic sp3C-H activation

A magnetite-reduced graphene oxide-supported CuO nanocomposite (rGO/Fe3O4-CuO) was preparedviaa facile chemical method and characterized by Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), UV-vis spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive spectroscopy (EDS), Brunauer-Emmett-Teller (BET) analysis, vibrating-sample magnetometry (VSM), and thermogravimetric (TG) analysis. The catalytic activity of the rGO/Fe3O4-CuO nanocomposite was probed in the direct oxidative amidation reaction of methylarenes with free amines. Various aromatic and aliphatic amides were prepared efficiently at room temperature from cheap raw chemicals usingtert-butyl hydroperoxide (TBHP) as a “green” oxidant and low-toxicity TBAI in water. This method combines the oxidation of methylarenes and amide bond formation into a single operation. Moreover, the synthesized nanocomposites can be separated from the reaction mixtures using an external magnet and reused in six consecutive runs without a noticeable decrease in the catalytic activity.

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.

The copper-catalyzed cross-coupling reactions of aryl diazonium salts and isocyanides

The copper-catalyzed cross-coupling reaction of aryl diazonium salts and isocyanides has been performed. This is a successful example of preparation of arylcarboxyamides with moderate to good yield under mild conditions.