58164-14-0

Usage

Uses

Used in Pharmaceutical Industry:
2-Bromo-5-tert-butylaniline is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows it to be incorporated into the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Organic Dyes Industry:
In the organic dyes industry, 2-Bromo-5-tert-butylaniline is utilized as a key component in the production of dyes with specific color properties. Its aromatic amine and bromine atom provide the necessary characteristics for the creation of dyes with distinct hues and stability.
Used in Agrochemical Industry:
2-Bromo-5-tert-butylaniline is employed as a building block in the synthesis of agrochemicals, such as pesticides and herbicides. Its chemical properties enable the development of effective and targeted agrochemicals for agricultural applications.
Used in Rubber Chemicals Industry:
In the rubber chemicals industry, 2-Bromo-5-tert-butylaniline is used in the manufacturing of various rubber additives and accelerators. Its presence in these compounds enhances the properties of rubber, such as durability and resistance to environmental factors.
Used in Other Industrial Products:
Beyond the aforementioned industries, 2-Bromo-5-tert-butylaniline also finds applications in the production of other industrial products. Its versatility as a chemical intermediate allows it to be incorporated into a wide range of products, contributing to the development and improvement of various materials and compounds.

Upstream product

• 70729-05-4 1-Bromo-4-tert-butyl-2-nitro-benzene 
• 3972-65-4 1-bromo-4-tert-butylbenzene 

Downstream Products

• 1597602-47-5 C₃₀H₃₃FN₂O₂ 
• 1597601-98-3 2-(2-fluoro-4-tertbutylphenyl)-5-nitrobenzophenone 
• 1597601-93-8 potassium 2-fluoro-4-tertbutylphenyltrifluoroboronate 
• 1597602-03-3 3-tertbutyl-5-(cyclohexylmethyl)-6-phenyl-8-nitrophenanthridinium chloride 
• 1369829-80-0 1-bromo-2-fluoro-4-tertbutylbenzene 
• 1597601-99-4 {[2-(4-tertbutyl-2-fluorophenyl)-5-nitrophenyl](phenyl)methylidene}(hexyl)amine 
• 916747-52-9 (2-bromo-5-tert-butylphenyl)boronic acid 
• 916747-51-8 1-bromo-4-tert-butyl-2-iodobenzene1-bromo-4-tert-butyl-2-iodobenzene 

Relevant academic research and scientific papers

Synthesis of ladder-type graphene ribbon oligomers from pyrene units

A series of ladder-type graphene ribbon oligomers have been synthesized through DDQ/acid-mediated oxidative cyclization. The oligomers present a bright blue light emission, and the new oligomers were clearly characterized by NMR and MALDI-TOF.

Highly efficient dye-sensitized solar cells based on panchromatic ruthenium sensitizers with quinolinylbipyridine anchors

Panchromatic RuII sensitizers TF-30-TF-33 bearing a new class of 6-quinolin-8-yl-2,2′-bipyridine anchor were synthesized and tested under AM1.5 G simulated solar irradiation. Their increased π conjugation relative to that of the traditional 2,2

Expanding the palette of phenanthridinium cations

5,6-Disubstituted phenanthridinium cations have a range of redox, fluorescence and biological properties. Some properties rely on phenanthridiniums intercalating into DNA, but the use of these cations as exomarkers for the reactive oxygen species (ROS), superoxide, and as inhibitors of acetylcholine esterase (AChE) do not require intercalation. A versatile modular synthesis of 5,6-disubstituted phenanthridiniums that introduces diversity by Suzuki-Miyaura coupling, imine formation and microwave-assisted cyclisation is presented. Computational modelling at the density functional theory (DFT) level reveals that the novel displacement of the aryl halide by an acyclic N-alkylimine proceeds by an SNAr mechanism rather than electrocyclisation. It is found that the displacement of halide is concerted and there is no stable Meisenheimer intermediate, provided the calculations consistently use a polarisable solvent model and a diffuse basis set.

Selective reduction of halogenated nitroarenes with hydrazine hydrate in the presence of Pd/C

A large variety of halogenated nitroarenes have been selectively reduced with hydrazine hydrate in the presence of Pd/C to give the corresponding (halogenated) anilines in good yield.

AMINOPYRIMIDINONES AS INTERLEUKIN RECEPTOR-ASSOCIATED KINASE INHIBITORS

This invention relates to aminopyrimidinone compounds of Formula (I) that are inhibitors of Interleukin receptor-associated kinases, in particular IRAK-4, and are useful in the treatment or prevention of inflammatory diseases, including rheumatoid arthritis and inflammatory bowel disease.

Oligoindenopyrenes: A new class of polycyclic aromatics

(Graph Presented) A new class of polycyclic aromatic hydrocarbons - oligoindenopyrenes - has been synthesized featuring a Pd-catalyzed Suzuki - Heck coupling cascade. The oligoindenopyrenes are robust, highly colored substructures of C70 and have properties that might prove useful in new organic materials or devices. After excitation, the tetraindenopyrene derivative 3d undergoes efficient deactivation (99%) by internal conversion to the ground state. The small fluorescence quantum yield (0.004) is in accordance with the short (0.6 ns) fluorescence decay time.