16034-40-5

Usage

Uses

Used in Pharmaceutical Industry:
N,N-Diphenyl-4-methoxybenzamide is utilized as a pharmaceutical intermediate for the production of drugs, specifically those aimed at treating pain and inflammation. Its involvement in drug synthesis is attributed to its chemical properties that facilitate the development of effective medicinal compounds.
Used in Dye Production:
In the dye industry, N,N-Diphenyl-4-methoxybenzamide serves as an intermediate, contributing to the creation of a range of dyes with specific color characteristics and properties.
Used in Organic Synthesis:
As a reagent in organic synthesis, N,N-Diphenyl-4-methoxybenzamide is employed for its ability to form stable complexes with various metals, which is crucial in numerous chemical reactions and the synthesis of complex organic molecules.
Used as a Corrosion Inhibitor in Metal Coating Industry:
N,N-Diphenyl-4-methoxybenzamide has been studied for its potential as a corrosion inhibitor in metal coatings. Its application in this field is due to its capacity to protect metal surfaces from degradation, thereby extending the lifespan of metal structures and components.
Used as an Antifungal Agent in Agriculture:
In agricultural applications, N,N-Diphenyl-4-methoxybenzamide has been explored as an antifungal agent. Its use in this context is based on its potential to combat fungal infections in crops, thereby improving yield and crop health.

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

• 100-07-2 4-methoxy-benzoyl chloride 
• 122-39-4 diphenylamine 
• 7465-88-5 4-methoxy-N-phenylbenzamide 
• 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 
• 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 academic research and scientific papers

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.

A simple copper-catalyzed synthesis of tertiary acyclic amides

The N-arylation of aromatic and aliphatic secondary acyclic amides, known to be poor nucleophiles, has been accomplished using a simple and cheap copper catalytic system. The corresponding tertiary acyclic amides, which can be found in numerous biologically active compounds, have been obtained in good to excellent yields.

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

NUCLEAR RECEPTOR BINDING AGENTS

The present invention relates to a novel class of selective estrogen receptor modulators (SERMs). The SERM compounds are applicable for use in the prevention and/or treatment of a variety of diseases and conditions including prevention and treatment of cancers such as prostate and breast cancer, osteoporosis, hormone-related diseases, hot flashes or vasomotor symptoms, neurological disorders, cardiovascular disease and obesity.

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.

REARRANGEMENT OF NITRONES TO AMIDES USING CHLOROSULFONYL ISOCYANATE

Reaction of chlorosulfonyl isocyanate (CSI) with nitrones 1a-n and 5a,b has been studied. α,α,N-Triaryl nitrones 1a-n react with CSI to form the N,N-diaryl arylamides 3a-n and 4i-n in good yields.In the case of α-H,α,N-diaryl nitrones 5a,b however, two compounds viz., the rearranged product 11a,b and the 1,4-dihydro tetrazines 10a,b are formed.The effect of substituents on the rearrangement has been studied.It is found that the nature of the substituents has got a profound effect on the rearrangement.We have also noted that the rearrangement is independent of the syn or anti configurations of the nitrones.