322-68-9

Basic information

• Product Name: 5-Fluoro-2-nitro-N-phenylaniline
• Synonyms: 5-Fluoro-2-nitro-N-phenylaniline
• CAS NO: 322-68-9
• Molecular Formula: C₁₂H₉FN₂O₂
• Molecular Weight: 232.2104632
• Mol File: 322-68-9.mol
• Article Data: 10

Chemical Properties

• Melting Point: 93-94 °C
• Boiling Point: 343.6±32.0 °C(Predicted)
• Appearance: /
• Density: 1.353±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: -4.30±0.50(Predicted)
• CAS DataBase Reference: 5-Fluoro-2-nitro-N-phenylaniline(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Fluoro-2-nitro-N-phenylaniline(322-68-9)
• EPA Substance Registry System: 5-Fluoro-2-nitro-N-phenylaniline(322-68-9)

Safety Data

• Hazardous Substances Data: 322-68-9(Hazardous Substances Data)

Usage

General Description

5-Fluoro-2-nitro-N-phenylaniline is a specialty chemical compound with the formula of C12H9FN2O2. The appearance of this chemical is generally in the form of an off-white powder, and it is utilized primarily for industrial and research purposes. 5-Fluoro-2-nitro-N-phenylaniline is known for its unique properties such as a relatively high molecular weight of 238.21 g/mol and a melting point range of 49-51°C. For safety considerations,

Upstream product

• 446-35-5 2,4-Difluoronitrobenzene 
• 62-53-3 aniline 
• 364-53-4 4-fluoro-1,2-dinitro-benzene 
• 402-67-5 3-fluoro-1-nitrobenzene 
• 350-46-9 4-Fluoronitrobenzene 
• 591-50-4 iodobenzene 
• 2369-11-1 5-fluoro-2-nitroaniline 

Downstream Products

• 325-61-1 5-fluoro-N₁-phenylbenzene-1,2-diamine 
• 151386-47-9 4-Fluoro-N¹-(3-methyl-butyl)-N²-phenyl-benzene-1,2-diamine 
• 151620-68-7 3-Amino-7-fluoro-1-(3-methyl-butyl)-5-phenyl-1,5-dihydro-benzo[b][1,4]diazepine-2,4-dione 
• 151386-48-0 7-Fluoro-1-(3-methyl-butyl)-5-phenyl-3-(phenyl-hydrazono)-1,5-dihydro-benzo[b][1,4]diazepine-2,4-dione 
• 389-44-6 1-phenyl-6-fluoro-1H-benzo[d][1,2,3]triazole 
• 391-53-7 2-fluoro-9H-carbazole 
• 1338482-09-9 (S)-1-(6-fluoro-1-phenyl-1H-benzo[d]imidazol-2-yl)ethanamine 
• 1338482-07-7 (S)-tert-butyl 1-(6-fluoro-1-phenyl-1H-benzo[d]imidazol-2-yl)ethylcarbamate 
• 1393176-60-7 (S)-1-(6-fluoro-1-phenyl-1H-benzo[d]imidazol-2-yl)propan-1-amine 
• 1393176-61-8 [(S)-1-(6-fluoro-1-phenyl-1H-benzoimidazol-2-yl)propyl]carbamic acid tert-butyl ester 
• 1393181-02-6 (S)-N-(1-(6-fluoro-1-phenyl-1H-benzo[d]imidazol-2-yl)propyl)-7H-purin-6-amine 
• 1338482-08-8 (S)-tert-butyl 1-(5-fluoro-1-phenyl-1H-benzo[d]imidazol-2-yl)ethylcarbamate 
• 1393176-62-9 (S)-1-(5-fluoro-1-phenyl-1H-benzo[d]imidazol-2-yl)ethanamine 
• 1393176-63-0 [(S)-1-(5-fluoro-2-phenylaminophenylcarbamoyl)ethyl]carbamic acid tert-butyl ester 

Relevant articles and documents

-

-

Design, Synthesis, and Antifungal Activities of Novel Aromatic Carboxamides Containing a Diphenylamine Scaffold

A series of novel N-(2-(phenylamino)-4-fluorophenyl)-pyrazole-4-carboxamides 1-15 and aromatic carboxamides with a diphenylamine scaffold 16-29 were designed, synthesized, and evaluated for their antifungal activities. In vitro experiments showed that com

Oxidative nucleophilic aromatic amination of nitrobenzenes

Nitrobenzenes substituted with electron-acceptor groups such as halogen, nitro, trifluoromethyl, pentafluorosulfanyl, or cyano underwent oxidative nucleophilic substitution with lithium salts of arylamines to afford N-aryl-2-nitroanilines.