N-(3-Acetylphenyl)-2-fluorobenzamide

Base Information

• Chemical Name: N-(3-Acetylphenyl)-2-fluorobenzamide
• CAS No.: 303091-99-8
• Molecular Formula: C₁₅H₁₂FNO₂
• Molecular Weight: 257.264
• DSSTox Substance ID: DTXSID401288942
• Mol file: 303091-99-8.mol

Synonyms:N-(3-Acetylphenyl)-2-fluorobenzamide;303091-99-8;MFCD00745331;Cambridge id 6283136;DTXSID401288942;BBL037255;STK501643;AKOS000176601;VS-14025;CS-0314954;AB00104990-01;AH-034/01376053;SR-01000510224;SR-01000510224-1;Z30816257

Chemical Property of N-(3-Acetylphenyl)-2-fluorobenzamide

Chemical Property:

• XLogP3: 2.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 257.08520679
• Heavy Atom Count: 19
• Complexity: 345

Purity/Quality:

98%min ^*data from raw suppliers

N-(3-Acetylphenyl)-2-fluorobenzamide ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi

MSDS Files:

Useful:

• Canonical SMILES: CC(=O)C1=CC(=CC=C1)NC(=O)C2=CC=CC=C2F

Technology Process of N-(3-Acetylphenyl)-2-fluorobenzamide

There total 1 articles about N-(3-Acetylphenyl)-2-fluorobenzamide 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:

1-(3-aminophenyl)ethanone (99-03-6) + 2-Fluorobenzoyl chloride (393-52-2) → N-(3-acetylphenyl)-2-fluorobenzamide (303091-99-8)

Guidance literature:

With sodium hydroxide;

DOI:10.3109/14756366.2011.587416

Reference yield: 100.0%

Indole-3-carboxaldehyde (487-89-8,1228547-52-1) + N-(3-acetylphenyl)-2-fluorobenzamide (303091-99-8) → C25H18FNO2

Guidance literature:

C₁₅H₁₂FNO₂; With sodium hydroxide; In ethanol; water; for 0.166667h;

Indole-3-carboxaldehyde; In ethanol; water; at 25 ℃; for 24h;

DOI:10.3109/14756366.2012.743536

Reference yield: 79.0%

N-(3-acetylphenyl)-2-fluorobenzamide (303091-99-8) + 3-(1,2,3,6-tetrahydro-1-methylpyridin-4-yl)-2,4,6-trimethoxybenzaldehyde (1361455-25-5) → 2-fluoro-N-(3-((2E)-3-(3-(1,2,3,6-tetrahydro-1-methylpyridin-4-yl)-2,4,6-trimethoxyphenyl)acryloyl)phenyl)benzamide (1366408-12-9)

Guidance literature:

C₁₅H₁₂FNO₂; With sodium hydroxide; In ethanol; for 0.0833333h;

3-(1,2,3,6-tetrahydro-1-methylpyridin-4-yl)-2,4,6-trimethoxybenzaldehyde; In ethanol; at 20 ℃; for 24h;

DOI:10.3109/14756366.2011.587416

upstream raw materials:

1-(3-aminophenyl)ethanone

2-Fluorobenzoyl chloride

Downstream raw materials:

2-fluoro-N-(3-((2E)-3-(3-(1,2,3,6-tetrahydro-1-methylpyridin-4-yl)-2,4,6-trimethoxyphenyl)acryloyl)phenyl)benzamide

N-(3-((E)-3-(3-bromo-2,4,6-trimethoxyphenyl)acryloyl)phenyl)-2-fluorobenzamide

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