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Usage

Uses

Used in Organic Synthesis:
3-Bromo-4-iodoaniline is used as a reagent and building block in organic synthesis for the creation of various organic compounds. Its unique structure allows for versatile reactions and the formation of a wide range of products.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 3-Bromo-4-iodoaniline serves as a key intermediate in the synthesis of pharmaceuticals. Its presence in the molecular structure can influence the pharmacological properties of the final drug, contributing to the development of new therapeutic agents.
Used in Agrochemicals:
3-Bromo-4-iodoaniline is also utilized in the synthesis of agrochemicals, playing a crucial role in the development of pesticides and other agricultural chemicals. Its unique properties can enhance the effectiveness and selectivity of these compounds.
Used in Research and Development:
3-BROMO-4-IODOANILINE is employed in research and development for the production of various organic compounds. Its versatility and reactivity make it a valuable tool for exploring new chemical reactions and synthesizing novel molecules with potential applications in various industries.

Upstream product

• 591-19-5 m-Bromoaniline 
• 13296-94-1 2-bromo-4-nitroaniline 
• 7149-14-6 2-bromo-1-iodo-4-nitrobenzene 
• 100-01-6 4-nitro-aniline 

Downstream Products

• 860556-79-2 2-bromo-1,4-diiodobenzene 
• 849727-76-0 2,2'-dibromo-4-tert-butyl-[1,1';4',1'';4'',1''']quaterphenyl 
• 23742-81-6 1-(3-Bromo-4-iodo-phenyl)-3-(4-trifluoromethyl-phenyl)-urea 
• 849727-71-5 3-(bromo-4-iodophenyl)acetamide 

Relevant academic research and scientific papers

Rhodium-Catalyzed Synthesis and Optical Properties of Silicon-Bridged Arylpyridines

A convergent and regioselective synthesis of silicon-bridged 4-arylpyridines has been developed through a rhodium-catalyzed [2+2+2] cycloaddition of silicon-containing diynes with nitriles. The absorption and emission properties of these compounds have be

SUBSTITUTED POLYCYCLIC ANTIBACTERIAL COMPOUNDS

The present description relates to substituted polycyclic compounds of Formula (I), Formula (II) or Formula (III): wherein the dashed line represents an optional double bond and Rl, R2, R4, R5, R7, X and Z are as defined herein, and forms and compositions thereof, and also relates to uses of a compound of Formula (I), Formula (II) or Formula (III) or a form thereof and methods for treating or ameliorating Neisseria gonorrhoeae (N. gonorrhoeae) in a subject in need thereof comprising, administering an effective amount of the compound to the subject.

Highly fluorescent solid-state asymmetric spirosilabifluorene derivatives

A series of four asymmetrically aryl-substituted 9,9′-spiro-9- silabifluorene (SSF) derivatives, 2,2′-di-tert-butyl-7,7′-diphenyl- 9,9′-spiro-9-silabifluorene (PhSSF), 2,2′-di-tert-butyl-7,7′- dipyridin-2-yl-9,9′-spiro-9-silabifluorene (PySSF), 2,2′-di-tert- butyl-7,7′-dibiphenyl-4-yl-9,9′-spiro-9-silabifluorene (BPhSSF), and 2,2′-di-tert-butyl-7,7′-bis(2′,2″-bipyridin-6-yl)-9, 9′-spiro-9-silabifluorene (BPySSF) are prepared through the cyclization of the corresponding 2,2′-dilithiobiphenyls with silicon tetrachloride. These novel spiro-linked silacyclopentadienes (siloles) form transparent and stable amorphous films with relatively high glass transition temperatures (Tg = 203-228°C). The absorbance spectrum of each compound shows a significant bathochromic shift relative to that of the corresponding carbon analogue as a result of the effective σ*-π* conjugation between the σ* orbital of the exocyclic Si-C bond and the π* orbital of the oligoarylene fragment. Solid-state films exhibit intense violet-blue emission (λPL = 398-415 nm) with high absolute photoluminescence quantum yields (ΦPL = 30-55%).

Mild and efficient direct aromatic iodination

Aryl iodides are important synthetic intermediates that can be transformed into tritium labelled compounds by metal-mediated hydrodehalogenation and also react in a number of important synthetic transformations. We present ICl/In(OTf)3 as a new reagent combination for mild iodination, suitable for acid-sensitive substrates such as carbohydrates.