2-amino-N-(4-isopropylphenyl)benzamide

Base Information

• Chemical Name: 2-amino-N-(4-isopropylphenyl)benzamide
• CAS No.: 353255-15-9
• Molecular Formula: C16H18N2O
• Molecular Weight: 254.332
• Hs Code.: 2924299090
• DSSTox Substance ID: DTXSID10384500
• Wikidata: Q82176688
• Mol file: 353255-15-9.mol

Synonyms:2-amino-N-(4-isopropylphenyl)benzamide;353255-15-9;2-amino-N-(4-propan-2-ylphenyl)benzamide;Benzamide, 2-amino-N-[4-(1-methylethyl)phenyl]- (9CI);HMS550H20;Maybridge1_003166;Oprea1_644089;SCHEMBL2577563;DTXSID10384500;ZUWRVYUSVRFPPJ-UHFFFAOYSA-N;AKOS000125445;2-amino-N-(4-isopropyl-phenyl)-benzamide;AI-204/13222002

Chemical Property of 2-amino-N-(4-isopropylphenyl)benzamide

Chemical Property:

• PSA: 55.12000
• LogP: 4.29870
• XLogP3: 4.1
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 254.141913202
• Heavy Atom Count: 19
• Complexity: 295

Purity/Quality:

2-AMINO-N-[4-(PROPAN-2-YL)PHENYL]BENZAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)C1=CC=C(C=C1)NC(=O)C2=CC=CC=C2N

Technology Process of 2-amino-N-(4-isopropylphenyl)benzamide

There total 1 articles about 2-amino-N-(4-isopropylphenyl)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: 89.0%

isatoic anhydride (118-48-9) + 4-Isopropylaniline (99-88-7) → 2-amino-N-(4-isopropyl-phenyl)-benzamide (353255-15-9)

Guidance literature:

In N,N-dimethyl-formamide; at 60 ℃; for 6h;

DOI:10.1080/00304940509354986

Reference yield: 93.0%

2-amino-N-(4-isopropyl-phenyl)-benzamide (353255-15-9) + trifluoroacetyl chloride (76-02-8) → N-(4-isopropyl-phenyl)-2-(2,2,2-trichloro-acetylamino)-benzamide (625379-22-8)

Guidance literature:

With triethylamine; In tetrahydrofuran; for 4.5h; cooling;

DOI:10.1080/00304940509354986

Reference yield: 91.0%

2-amino-N-(4-isopropyl-phenyl)-benzamide (353255-15-9) + dimedone (126-81-8) → 2-((5,5-dimethyl-3-oxocyclohex-1-en-1-yl)amino)-N-(4-isopropylphenyl)benzamide (1422154-65-1)

Guidance literature:

With iodine; In toluene; at 50 ℃; for 8h;

DOI:10.1016/j.tetlet.2012.11.042

upstream raw materials:

isatoic anhydride

4-Isopropylaniline

Downstream raw materials:

2-[2-(5-Bromo-1H-indol-3-yl)-ethyl]-3-(4-isopropyl-phenyl)-3H-quinazolin-4-one

N-(4-isopropyl-phenyl)-2-(2,2,2-trichloro-acetylamino)-benzamide

2-(4-(2-hydroxyethoxy)-3,5-dimethylphenyl)-3-(4-isopropylphenyl)quinazolin-4(3H)-one

3-(4-isopropylphenyl)quinazolin-4(3H)-one

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