N-Ethylbenzanilide

Base Information

• Chemical Name: N-Ethylbenzanilide
• CAS No.: 16466-44-7
• Molecular Formula: C15H15 N O
• Molecular Weight: 225.29
• Hs Code.: 2924299090
• European Community (EC) Number: 240-511-8
• NSC Number: 406163
• UNII: 88FDH93SD6
• DSSTox Substance ID: DTXSID60167789
• Nikkaji Number: J318.199E
• Wikidata: Q83037248
• Mol file: 16466-44-7.mol

Synonyms:N-Ethylbenzanilide;N-ethyl-N-phenylbenzamide;16466-44-7;Benzamide, N-ethyl-N-phenyl-;EINECS 240-511-8;NSC-406163;AI3-01883;n -ethylbenzanilide;NSC406163;CBMicro_009312;88FDH93SD6;SCHEMBL1006444;DTXSID60167789;ADAL1186148;SMSF0005631;AKOS003283434;CB12420;NSC 406163;BIM-0009545.P001

Chemical Property of N-Ethylbenzanilide

Chemical Property:

• Vapor Pressure: 3.16E-05mmHg at 25°C
• Boiling Point: 355.3°C at 760 mmHg
• Flash Point: 159.7°C
• PSA: 20.31000
• Density: 1.107g/cm³
• LogP: 3.35330
• XLogP3: 2.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 225.115364102
• Heavy Atom Count: 17
• Complexity: 239

Purity/Quality:

99% ^*data from raw suppliers

N-ETHYL-N-PHENYLBENZAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCN(C1=CC=CC=C1)C(=O)C2=CC=CC=C2

Technology Process of N-Ethylbenzanilide

There total 50 articles about N-Ethylbenzanilide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 99.0%

N-phenyl benzoyl amide (93-98-1,5705-51-1) + triethyl phosphate (78-40-0) → N-ethyl-N-phenylbenzamide (16466-44-7)

Guidance literature:

With lithium diisopropyl amide; In tetrahydrofuran; at 0 - 75 ℃; for 24h; regioselective reaction;

DOI:10.1055/a-1504-8366

Reference yield: 95.0%

N-phenyl benzoyl amide (93-98-1,5705-51-1) + diethyl sulfate (64-67-5) → N-ethyl-N-phenylbenzamide (16466-44-7)

Guidance literature:

With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; In benzene; at 80 ℃; for 3h;

Reference yield: 92.0%

N-phenyl benzoyl amide (93-98-1,5705-51-1) + ethyl iodide (75-03-6) → N-ethyl-N-phenylbenzamide (16466-44-7)

Guidance literature:

With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; In benzene; at 70 ℃; for 4h;

upstream raw materials:

N-ethyl-N-phenyl-urea

benzoyl chloride

N-ethyl-N-phenylamine

N,N-diethylaniline

Downstream raw materials:

N-ethyl-N-trityl-aniline

benzophenone

N-ethyl-N-phenylamine

N-ethyl-thiobenzanilide

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