2-fluoro-N-methyl-5-nitrobenzamide

Base Information

• Chemical Name: 2-fluoro-N-methyl-5-nitrobenzamide
• CAS No.: 136146-83-3
• Molecular Formula: C8H7FN2O3
• Molecular Weight: 198.154
• Hs Code.: 2924299090
• DSSTox Substance ID: DTXSID10655944
• Wikidata: Q82570336
• Mol file: 136146-83-3.mol

Synonyms:2-fluoro-N-methyl-5-nitrobenzamide;136146-83-3;AB3780;SCHEMBL17192840;DTXSID10655944;MFCD09909408;AKOS005063182;AS-44735;EN300-51520;Z415710380

Chemical Property of 2-fluoro-N-methyl-5-nitrobenzamide

Chemical Property:

• Boiling Point: 316.7±32.0 °C(Predicted)
• PKA: 13.14±0.46(Predicted)
• PSA: 78.41000
• Density: 1.358±0.06 g/cm3(Predicted)
• LogP: 2.19150
• XLogP3: 1.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 1
• Exact Mass: 198.04407025
• Heavy Atom Count: 14
• Complexity: 241

Purity/Quality:

98%min ^*data from raw suppliers

2-fluoro-N-methyl-5-nitrobenzamide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CNC(=O)C1=C(C=CC(=C1)[N+](=O)[O-])F

Technology Process of 2-fluoro-N-methyl-5-nitrobenzamide

There total 1 articles about 2-fluoro-N-methyl-5-nitrobenzamide 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: 93.0%

2-fluoro-5-nitrobenzoic acid (7304-32-7) + methylamine hydrochloride (593-51-1) → 2-fluoro-N-methyl-5-nitrobenzamide (136146-83-3)

Guidance literature:

With triethylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In dichloromethane; at 20 ℃;

Reference yield: 71.0%

morpholine (110-91-8,99108-56-2) + 2-fluoro-N-methyl-5-nitrobenzamide (136146-83-3) → N-methyl-2-morpholino-5-nitrobenzamide

Guidance literature:

With caesium carbonate; In dimethyl sulfoxide; at 80 ℃;

Reference yield: 50.0%

1-methyl-piperazine (109-01-3) + 2-fluoro-N-methyl-5-nitrobenzamide (136146-83-3) → N-methyl-2-(4-methylpiperazin-1-yl)-5-nitrobenzamide

Guidance literature:

With caesium carbonate; In dimethyl sulfoxide; at 85 ℃;

upstream raw materials:

2-fluoro-5-nitrobenzoic acid

methylamine hydrochloride