Benzanilide, N-benzyl-

Base Information

• Chemical Name: Benzanilide, N-benzyl-
• CAS No.: 19672-91-4
• Molecular Formula: C20H17NO
• Molecular Weight: 287.361
• European Community (EC) Number: 633-731-4
• DSSTox Substance ID: DTXSID00173344
• Nikkaji Number: J390.230G
• Wikidata: Q83043399
• Mol file: 19672-91-4.mol

Synonyms:Benzanilide, N-benzyl-;n-benzyl-n-phenylbenzamide;N-Benzylbenzanilide;19672-91-4;Benzamide, N-phenyl-N-(phenylmethyl)-;BRN 2380199;AI3-01077;C20H17NO;N-Benzyl-N-benzoylaniline;N-benzyl-N-phenyl benzamide;SCHEMBL8332050;DTXSID00173344;ADAL1038685;AKOS007971763;LS-27610;AG-205/05289040;Z26619709

Chemical Property of Benzanilide, N-benzyl-

Chemical Property:

• Vapor Pressure: 1.83E-08mmHg at 25°C
• Boiling Point: 455°Cat760mmHg
• Flash Point: 211.3°C
• Density: 1.16g/cm³
• XLogP3: 4.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 287.131014166
• Heavy Atom Count: 22
• Complexity: 336

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C1=CC=C(C=C1)CN(C2=CC=CC=C2)C(=O)C3=CC=CC=C3

Technology Process of Benzanilide, N-benzyl-

There total 24 articles about Benzanilide, N-benzyl- 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: 98.0%

N-phenyl benzoyl amide (93-98-1,5705-51-1) + tribenzylphosphate (1707-92-2) → N-benzyl-N-phenylbenzamide (19672-91-4)

Guidance literature:

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

DOI:10.1055/a-1504-8366

Reference yield: 97.0%

benzyl chloride (100-44-7) + benzanilide ion (61057-09-8) → N-benzyl-N-phenylbenzamide (19672-91-4)

Guidance literature:

In dimethyl sulfoxide; at 25 ℃; for 45h;

DOI:10.1021/ja00323a029

Reference yield: 92.0%

N-phenyl benzoyl amide (93-98-1,5705-51-1) + benzyl chloride (100-44-7) → N-benzyl-N-phenylbenzamide (19672-91-4)

Guidance literature:

With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; In benzene; at 80 ℃; for 2.5h;

upstream raw materials:

N,N-dibenzylaniline

N-Benzylaniline

benzoyl chloride

benzylidene phenylamine

Downstream raw materials:

N-benzyl-thiobenzanilide

N-phenyl benzoyl amide

benzyl chloride

N-benzyl-2-hydroxy-N-phenylbenzamide

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