58534-94-4

Usage

Uses

Used in Pharmaceutical Industry:
3-Bromo-2-fluoronitrobenzene is used as a key intermediate in the synthesis of pharmaceutical drugs for its ability to be transformed into a variety of medicinal compounds through organic synthesis.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Bromo-2-fluoronitrobenzene serves as a precursor in the production of agrochemicals, contributing to the development of effective crop protection agents.
Used in Organic Synthesis:
3-Bromo-2-fluoronitrobenzene is utilized as a building block in organic synthesis, allowing for the creation of a wide range of other useful compounds through various chemical reactions.

InChI:InChI=1/C6H3BrFNO2/c7-4-2-1-3-5(6(4)8)9(10)11/h1-3H

Upstream product

• 3970-37-4 1-bromo-2-chloro-3-nitrobenzene 
• 3970-35-2 2-chloro-3-nitrobezoic acid 
• 59255-95-7 2-bromo-6-nitroaniline 
• 615-36-1 2-bromoaniline 
• 614-76-6 N-acetyl-2-bromoaniline 

Downstream Products

• 1189042-70-3 2-(2-fluoro-3-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 741721-37-9 5-(2-fluoro-3-nitro-phenyl)-pent-4-ynoic acid methyl ester 
• 873697-74-6 C₉H₈FNO₃ 
• 1025392-74-8 (4-bromo-2-nitro-phenyl)-(1-pyrimidin-2-yl-piperidin-4-yl)-amine 
• 958489-03-7 (S)-3-(2-bromo-6-nitrophenoxy)-2-(tert-butoxycarbonylamino)propanoic acid 
• 1004618-77-2 2-bromo-N-methyl-6-nitro-aniline 
• 58534-95-5 3-bromo-2-fluorobenzenamine 
• 1269233-04-6 N-(3-bromo-2-fluorophenyl)propane-1-sulfonamide 
• 1269233-05-7 N-(3-bromo-2-fluorophenyl)-3,3,3-trifluoropropane-1-sulfonamide 
• 1231892-80-0 2-fluoro-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenylamine 
• 1400220-48-5 1-[2-fluoro-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-3-(4-chlorophenyl)-urea 
• 5320-98-9 N-(2-nitrophenyl)morpholine 
• 5585-33-1 2-morpholinoaniline 
• 1884712-47-3 CPI-637 

Relevant academic research and scientific papers

3-bromo-2-fluoronitrobenzene preparation method

The invention discloses a 3-bromo-2-fluoronitrobenzene preparation method. The method includes steps: (1) under the alkali action, subjecting bromoaniline and acetyl chloride to acetylation to obtainN-(2-bromophenyl)acetamide; (2) subjecting N-(2-bromophe

Synthesis and structure-activity studies of novel benzocycloheptanone oxazolidinone antibacterial agents

We describe a novel class of benzocycloheptanone derived oxazolidinone antibacterial agents. The synthesis and antibacterial activities with structure variation is discussed.

ANTIBACTERIAL AGENTS

Compounds of formula I and methods for their preparation are disclosed. Further disclosed are methods of making biologically active compounds of formula I as well as pharmaceutically acceptable compositions comprising compounds of formula I. Compounds of formula I as disclosed herein can be used in a variety of applications including use as antibacterial agents.