16034-40-5

Basic information

• Product Name: N,N-DIPHENYL-4-METHOXYBENZAMIDE
• Synonyms: N-P-ANISOYLDIPHENYLAMINE;N,N-DIPHENYL-4-METHOXYBENZAMIDE;Diphenylmethoxybenzamide;N,N-Diphenyl-p-methoxybenzamide;4-Methoxy-N,N-diphenylbenzamide
• CAS NO: 16034-40-5
• Molecular Formula: C₂₀H₁₇NO₂
• Molecular Weight: 303.35
• Product Categories: Condensation & Active Esterification;Synthetic Organic Chemistry
• Mol File: 16034-40-5.mol
• Article Data: 6

Chemical Properties

• Melting Point: 140 °C
• Boiling Point: 468.2 °C at 760 mmHg
• Flash Point: 237 °C
• Appearance: /
• Density: 1.178
• Vapor Pressure: 6.11E-09mmHg at 25°C
• Refractive Index: 1.633
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: N,N-DIPHENYL-4-METHOXYBENZAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-DIPHENYL-4-METHOXYBENZAMIDE(16034-40-5)
• EPA Substance Registry System: N,N-DIPHENYL-4-METHOXYBENZAMIDE(16034-40-5)

Safety Data

• Hazardous Substances Data: 16034-40-5(Hazardous Substances Data)

Usage

General Description

N,N-Diphenyl-4-methoxybenzamide is a chemical compound with the molecular formula C20H17NO2. It is a white to off-white solid that is commonly used as an intermediate in the production of pharmaceuticals, dyes, and other organic compounds. N,N-DIPHENYL-4-METHOXYBENZAMIDE is often employed as a reagent in organic synthesis and is known for its ability to form stable complexes with various metals. It is also used as a pharmaceutical intermediate in the production of drugs, particularly those for treating pain and inflammation. Additionally, N,N-Diphenyl-4-methoxybenzamide has been studied for its potential use in various applications, including its use as a corrosion inhibitor in metal coatings and as an antifungal agent in agriculture.

InChI:InChI=1/C20H17NO2/c1-23-19-14-12-16(13-15-19)20(22)21(17-8-4-2-5-9-17)18-10-6-3-7-11-18/h2-15H,1H3

Upstream product

• 7465-88-5 4-methoxy-N-phenylbenzamide 
• 100-07-2 4-methoxy-benzoyl chloride 
• 62-53-3 aniline 
• 591-50-4 iodobenzene 
• 38968-72-8 N-phenyl-(4-methoxypheny)acetimidoyl chloride 
• 1189-71-5 isocyanate de chlorosulfonyle 
• 108438-77-3 α,N-diphenyl-α-(4-methoxyphenyl) nitrone 
• 122-39-4 diphenylamine 
• 1089303-32-1 4-methoxy-N-phenyl-benzimidic acid phenyl ester 

Downstream Products

• 148963-14-8 N-(4-methoxybenzyl)-N,N-diphenylamine 
• 132058-85-6 (3,4-Dimethoxy-phenyl)-(4-phenylamino-phenyl)-methanone 
• 126762-87-6 (3-Nitro-phenyl)-(4-phenylamino-phenyl)-methanone 
• 126762-88-7 9-(3-Nitrobenzoyl)-acridine 
• 132058-88-9 9-(3,4-Dimethoxy-phenyl)-acridine 
• 132058-86-7 9-(2-Methoxyphenyl)-acridine 
• 108350-92-1 N-(2-Iodobenzoyl)-diphenylamine 
• 86-74-8 9H-carbazole 
• 1522-69-6 N-(3,4-Dimethoxybenzoyl)-diphenylamine 
• 73333-82-1 N-(3-Nitrobenzoyl)-diphenylamine 
• 94623-43-5 N-(2-Methoxybenzoyl)-diphenylamine 
• 95425-88-0 N-(3-Methoxybenzoyl)-diphenylamine 
• 13355-65-2 5-phenylphenanthridin-6(5H)-one 
• 85121-13-7 N,N-diphenyl-p-methoxyphenylchloromethyleniminium chloride 

Relevant articles and documents

Efficient synthesis of tertiary acyclic amides by the Chapman rearrangement of aryl benzimidates in ionic liquids

The Chapman rearrangement of aryl N-arylbenzimidates to tertiary acyclic amides is accelerated in ionic liquids and proceeds at lower temperatures as 120-190°C.

Highly chemoselective metal-free reduction of tertiary amides

This communication describes the chemoselective metal-free reduction of tertiary amides to the corresponding amines. Hantzsch ester is used as a mild reducing agent for the reduction of trifluoromethanesulfonic anhydride activated amides providing the tertiary amines with high functional group tolerance. Copyright

STUDIES ON ENAMIDES. PART 4 : PHOTOCHEMICAL INVESTIGATIONS OF N-AROYLDIPHENYLAMINES

Photolysis of N-aroyldiphenylamines affords 9-arylacridines or phenanthridinone depending on the structure of the substrates.Additionally, carbazole and photomigrated products are also obtained.