898128-02-4

Usage

Uses

Used in Pharmaceutical Industry:
1,3-Dibromo-5-fluoro-2-nitrobenzene is used as a building block in organic synthesis for the development of new pharmaceuticals. Its unique structure and reactivity allow for the creation of diverse drug candidates with potential therapeutic applications.
Used in Chemical Industry:
In the chemical industry, 1,3-Dibromo-5-fluoro-2-nitrobenzene serves as an important intermediate in the production of various organic compounds. Its properties make it suitable for use in the synthesis of specialty chemicals and other complex molecules.
Used in Agrochemical Production:
1,3-Dibromo-5-fluoro-2-nitrobenzene is utilized as a key intermediate in the synthesis of agrochemicals. Its role in the production of these chemicals contributes to the development of effective pesticides and other agricultural products.

Upstream product

• 344-18-3 2,6-dibromo-4-fluoroaniline 

Downstream Products

• 1276583-73-3 3,5-dibromo-N,N-dimethyl-4-nitroaniline 
• 1281994-78-2 2,6-dibromo-4-(N,N-dimethylamino)aniline 
• 1281994-94-2 C₆₀H₅₀N₄ 

Relevant academic research and scientific papers

LIPOXYGENASE INHIBITORS

Various embodiments of the present disclosure are directed to compounds having Formula I, Formula II, Formula IIA, Formula III, Formula IIIA, Formula IIIB, and/or pharmaceutically acceptable salts thereof. The compounds can be suitable for inhibiting lipoxygenases and/or treating associated diseases. In some embodiments, subject compounds are used to prepare a composition that is effective in treating neurodegenerative diseases.

Systematic investigation of ligand substitution effects in cyclophane-based nickel(II) and palladium(II) olefin polymerization catalysts

The synthesis of Ni(II) and Pd(II) cyclophane-based α-diimine olefin polymerization catalysts bearing a range of electron-donating or -withdrawing groups is described. Substituent effects were confirmed by measurement of CO infrared stretching frequencies

Selective oxidation of aromatic amines to nitro derivatives using potassium iodide-tert-butyl hydroperoxide catalytic system

The direct oxidation of aromatic primary amines to the corresponding nitro compounds selectively in 47-98% yields has been achieved by using potassium iodide as catalyst and tert-butyl hydroperoxide as the external oxidant. The present catalytic system works well for both electron-rich and electron-poor substrates.