63037-64-9

Usage

Uses

Used in Organic Synthesis:
4-Bromo-3-iodoaniline is used as a building block for the synthesis of various organic compounds due to its ability to introduce both bromine and iodine atoms into target molecules. This dual-halogen substitution capability enhances the reactivity and functionalization potential of the resulting compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-Bromo-3-iodoaniline serves as a key intermediate in the development of new drugs. Its unique chemical properties allow for the creation of pharmaceutical compounds with specific therapeutic effects, contributing to the advancement of medicinal chemistry.
Used in Chemical Research:
4-Bromo-3-iodoaniline is utilized in chemical research to explore the effects of halogen substitution on the properties and reactivity of aromatic compounds. This research aids in understanding the fundamental principles of organic chemistry and contributes to the discovery of new chemical reactions and processes.
Used in Material Science:
4-BroMo-3-iodoaniline's unique properties also make it a candidate for the development of new materials with specific characteristics, such as improved conductivity, stability, or reactivity. This application can lead to innovations in various fields, including electronics, energy, and environmental science.

Upstream product

• 10403-47-1 2-bromo 5-nitroaniline 
• 106-40-1 4-bromo-aniline 
• 626-01-7 3-Iodoaniline 
• 62-53-3 aniline 
• 63037-63-8 1-bromo-2-iodo-4-nitrobenzene 

Downstream Products

• 137840-24-5 2-[(4-Bromo-3-iodo-phenylcarbamoyl)-methyl]-benzoic acid 
• 1291063-32-5 4-bromo-3-iodo-N,N-dimethylaniline 
• 1036750-83-0 6-bromo-[1,1'-biphenyl]-3-amine 

Relevant academic research and scientific papers

AN IMPROVED ONE POT, ONE STEP PROCESS FOR THE HALOGENATION OF AROMATICS USING SOLID ACID CATALYSTS

The present invention disclosed an improved one pot, one step process for halogenation of compound of formula (II) to afford corresponding halogenated compound of formula (I) having improved yield and increased selectivity under very mild conditions.

Through the maze: Cross-coupling pathways to a helical hexaphenyl "Gel?nder" molecule

This paper highlights a new concept on how to induce chirality in a hexaphenyl Gel?nder-type system. Bridging a terphenyl backbone with a considerably longer benzyl ether oligomer enforces a continuous twist of the molecule, while preventing an achiral me

Inducing axial chirality in a "Gel?nder" oligomer by length mismatch of the oligomer strands

Helical molecules are not only esthetically appealing due to their structural beauty, they also display unique physical properties as a result of their chirality.We describe herein a new approach to "Gel?nder" oligomers by interlinking two oligomer strand

FUSED AROMATIC PTP-1B INHIBITORS

The invention encompasses the novel class of compounds represented by the formula below, which are inhibitors of the PTP-1B enzyme. The invention also encompasses pharmaceutical compositions which include the compounds shown (Formula I) above and methods of treating or preventing PTP-1B mediated diseases, including diabetes.