16466-44-7

Basic information

• Product Name: N-ethylbenzanilide
• Synonyms: N-ethylbenzanilide;N-Ethyl-N-phenylbenzamide
• CAS NO: 16466-44-7
• Molecular Formula: C₁₅H₁₅NO
• Molecular Weight: 225.2857
• EINECS: 240-511-8
• Mol File: 16466-44-7.mol
• Article Data: 29

Chemical Properties

• Boiling Point: 355.3°C at 760 mmHg
• Flash Point: 159.7°C
• Appearance: /
• Density: 1.107g/cm³
• Vapor Pressure: 3.16E-05mmHg at 25°C
• Refractive Index: 1.606
• CAS DataBase Reference: N-ethylbenzanilide(CAS DataBase Reference)
• NIST Chemistry Reference: N-ethylbenzanilide(16466-44-7)
• EPA Substance Registry System: N-ethylbenzanilide(16466-44-7)

Safety Data

• Hazardous Substances Data: 16466-44-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C15H15NO/c1-2-16(14-11-7-4-8-12-14)15(17)13-9-5-3-6-10-13/h3-12H,2H2,1H3

Upstream product

• 63098-95-3 N-ethyl-N-phenyl-urea 
• 98-88-4 benzoyl chloride 
• 103-69-5 N-ethyl-N-phenylamine 
• 91-66-7 N,N-diethylaniline 
• 93-98-1 N-phenyl benzoyl amide 
• 64-67-5 diethyl sulfate 
• 14752-72-8 1,N-Diphenylpropanimine 
• 75-03-6 ethyl iodide 
• 591-50-4 iodobenzene 
• 201230-82-2 carbon monoxide 
• 65-85-0 benzoic acid 
• 618-38-2 benzoyl iodide 
• 613-97-8 N-methyl-N-ethylaniline 
• 100-52-7 benzaldehyde 

Downstream Products

• 861526-55-8 N-ethyl-N-trityl-aniline 
• 119-61-9 benzophenone 
• 103-69-5 N-ethyl-N-phenylamine 
• 83890-07-7 N-ethyl-thiobenzanilide 
• 100-52-7 benzaldehyde 
• 92-59-1 N-benzyl-N-ethylaniline 
• 111383-50-7 N-ethyl-2-hydroxy-N-phenylbenzamide 
• 17646-87-6 benzoic acid-(N-ethyl-2-hydroxy-anilide) 
• 59238-66-3 N-(4-(tert?butyl)phenyl)benzamide 
• 582-78-5 N-(4-methylphenyl)benzamide 
• 54343-55-4 3-Benzoyl-1-methyl-2-pyrrolidinone 
• 100-51-6 benzyl alcohol 
• 53145-32-7 N-vinyl benzanilide 

Relevant articles and documents

Palladium-Catalyzed Desulfurative Hiyama Coupling of Thioureas to Achieve Amides via Selective C-N Bond Cleavage

Palladium-catalyzed Hiyama coupling of active thioureas via selective C-N bond cleavage is reported. Notably, the new approach employed active thioureas as coupling partners in the presence of arylsilanes to give amides in good yield. Further, this strategy, which utilized CuF 2as a key oxidant and activator, afforded various amide products under mild conditions and an easy to handle procedure without extra base.

Nickel-Catalyzed Oxidative Transamidation of Tertiary Aromatic Amines with N -Acylsaccharins

The use of tertiary amines as surrogates for secondary amines has prominent advantages in terms of stabilization and ease of handling. A Ni-catalyzed transamidation of N -acylsaccharins with tertiary aromatic amines is reported. By using tert -butyl hydroperoxide as the terminal oxidant, this reaction permits selective cleavage of the C(sp 3)-N bonds of unsymmetrical tertiary aromatic amines depending on the sizes of the alkyl substituents.

Preparation of alkylated compounds using the trialkylphosphate

[Problem] trialkylphosphate strong base used reaction agent, a carboxylic acid, a ketone, an aldehyde, amine, amide, thiol, ester or Grignard reagent to a variety of substrates, and/or high efficiency to generate a highly stereoselective alkylation reaction, the alkylated compounds capable of producing new means. [Solution] was used as the alkylating agent in the alkylation of compound trialkylphosphate, strongly basic reaction production use. [Drawing] no