Benzamide, N-[2-(1-methylethenyl)phenyl]-

Base Information

• Chemical Name: Benzamide, N-[2-(1-methylethenyl)phenyl]-
• CAS No.: 106012-41-3
• Molecular Formula: C16H15NO
• Molecular Weight: 237.301
• DSSTox Substance ID: DTXSID50455864
• Nikkaji Number: J2.346.089K
• Wikidata: Q82278019

Synonyms:Benzamide, N-[2-(1-methylethenyl)phenyl]-;106012-41-3;SCHEMBL15079054;DTXSID50455864;N-(2-Isopropenylphenyl)benzamide

Chemical Property of Benzamide, N-[2-(1-methylethenyl)phenyl]-

Chemical Property:

• XLogP3: 4.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 237.115364102
• Heavy Atom Count: 18
• Complexity: 304

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=C)C1=CC=CC=C1NC(=O)C2=CC=CC=C2

Technology Process of Benzamide, N-[2-(1-methylethenyl)phenyl]-

There total 12 articles about Benzamide, N-[2-(1-methylethenyl)phenyl]- 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%

2-isopropenylaniline (52562-19-3) + benzoyl chloride (98-88-4) → N-[2-(1-methylethenyl)phenyl]benzamide (106012-41-3)

Guidance literature:

With triethylamine; In dichloromethane; at 0 ℃;

DOI:10.1039/d0ob00233j

Reference yield: 67.0%

2'-acetylbenzanilide (6011-26-3) + methyltriphenylphosphonium bromide → N-[2-(1-methylethenyl)phenyl]benzamide (106012-41-3)

Guidance literature:

methyltriphenylphosphonium bromide; With sodium t-butanolate; In diethyl ether; at 0 ℃; for 1h;

2'-acetylbenzanilide; In diethyl ether; at 0 ℃; Reflux;

DOI:10.1002/adsc.201701386

Reference yield: 51.0%

4-Methyl-4-methylsulfanylmethyl-2-phenyl-4H-benzo[d][1,3]oxazine (106012-47-9) → N-[2-(1-methylethenyl)phenyl]benzamide (106012-41-3)

Guidance literature:

With acetic acid; zinc; for 1h; Heating;

upstream raw materials:

2-isopropenylaniline

benzoyl chloride

4-Methyl-4-methylsulfanylmethyl-2-phenyl-4H-benzo[d][1,3]oxazine

1-(1-methylethenyl)-2-nitrobenzene

Downstream raw materials:

4-methyl-2-phenylquinoline

4,4-dimethyl-2-phenyl-4H-benzo[d][1,3]oxazine

4-Methyl-4-methylsulfanylmethyl-2-phenyl-4H-benzo[d][1,3]oxazine

2-benzamido-1-isopropylbenzene

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