N-(3,5-dimethylphenyl)benzamide

Base Information

• Chemical Name: N-(3,5-dimethylphenyl)benzamide
• CAS No.: 25050-22-0
• Molecular Formula: C15H15NO
• Molecular Weight: 225.29
• DSSTox Substance ID: DTXSID90367972
• Nikkaji Number: J1.590.574C
• Wikidata: Q82154206
• ChEMBL ID: CHEMBL473677
• Mol file: 25050-22-0.mol

Synonyms:N-(3,5-dimethylphenyl)benzamide;25050-22-0;CHEMBL473677;SCHEMBL3274053;DTXSID90367972;PPCBJAXGIPETIF-UHFFFAOYSA-N;AKOS001218440;Z30889741

Chemical Property of N-(3,5-dimethylphenyl)benzamide

Chemical Property:

• XLogP3: 3.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 225.115364102
• Heavy Atom Count: 17
• Complexity: 248

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC(=CC(=C1)NC(=O)C2=CC=CC=C2)C

Technology Process of N-(3,5-dimethylphenyl)benzamide

There total 33 articles about N-(3,5-dimethylphenyl)benzamide 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: 100.0%

triphenylboroxine (3262-89-3) + benzyl 3,5-(dimethyl)phenylcarbamate → N-(3,5-dimethylphenyl)-benzamide (25050-22-0)

Guidance literature:

With potassium fluoride; chloro(1,5-cyclooctadiene)rhodium(I) dimer; In 1,4-dioxane; at 100 ℃; for 24h; Inert atmosphere; Sealed tube;

DOI:10.1021/acs.orglett.5b03061

Reference yield: 99.0%

3,5-dimethylphenyl iodide (22445-41-6) + benzamide (55-21-0,27208-38-4) → N-(3,5-dimethylphenyl)-benzamide (25050-22-0)

Guidance literature:

With copper(l) iodide; N,N`-dimethylethylenediamine; In tetrahydrofuran; at 25 ℃; for 7h;

DOI:10.1021/ja0260465

Reference yield: 98.0%

benzoyl chloride (98-88-4) + 3,5-dimethylaminoaniline (108-69-0) → N-(3,5-dimethylphenyl)-benzamide (25050-22-0)

Guidance literature:

With dmap; triethylamine; In dichloromethane; at 0 - 20 ℃; for 6h;

DOI:10.1002/jhet.5570390517

upstream raw materials:

benzoyl chloride

3,5-dimethylaminoaniline

3,5-dimethylphenyl iodide

benzamide

Downstream raw materials:

N-benzyl-3,5-dimethylaniline

(E)-3,5-Dimethyl-2-(1'-propenyl)-anilin

(Z)-3,5-Dimethyl-2-(1'-propenyl)-anilin

2-allyl-3,5-dimethylaniline

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