53358-54-6

Usage

Uses

Used in Organic Synthesis:
Benzenamine, 4-bromo-N,N-dibutylis used as an intermediate in organic synthesis for the production of various chemical compounds. Its unique structure allows it to be a versatile building block in the synthesis of a wide range of organic molecules.
Used in Chemical Research:
This brominated aromatic amine is also utilized in chemical research to study the properties and reactions of brominated compounds. It can provide valuable insights into the behavior of similar compounds and contribute to the development of new synthetic methods and applications.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, benzenamine, 4-bromo-N,N-dibutyl-, may have potential applications in the pharmaceutical industry as a precursor for the synthesis of active pharmaceutical ingredients or as a building block for the development of new drugs.
Used in Dye Production:
As a derivative of aniline, benzenamine, 4-bromo-N,N-dibutyl-, can be used in the production of dyes. Its unique properties may contribute to the development of new dyes with specific color characteristics or improved performance.
Used in Rubber Chemicals:
Benzenamine, 4-bromo-N,N-dibutyl-, can also be used in the production of rubber chemicals, where it may serve as a key component in the synthesis of additives or other compounds that enhance the properties of rubber materials.

Upstream product

• 613-29-6 N-Dibutylaniline 
• 109-72-8 n-butyllithium 
• 75-77-4 chloro-trimethyl-silane 
• 1159339-41-9 2,4,6-tribromo-N,N-bis(trimethylsilyl)aniline 
• 109-65-9 1-bromo-butane 
• 106-40-1 4-bromo-aniline 
• 615-36-1 2-bromoaniline 
• 62-53-3 aniline 
• 542-69-8 1-iodo-butane 

Downstream Products

• 92726-05-1 4-(di(n-butyl)amino)benzoic acid 
• 500337-14-4 4,4'-bis-dibutylamino-benzophenone-imine 
• 90133-94-1 trans-4-pyridine 
• 147645-78-1 6-<4-(dibutylamino)phenyl>isoquinoline 
• 439248-53-0 7-(4-N,N-di-n-butylaminophenyl)-2,3,4,4a,5,6-hexahydronaphthalen-2-one 
• 4182-80-3 N,N,N’,N’-tetrakis[p-di(butyl)aminophenyl]-p-phenylene 
• 1374412-05-1 (4-(dibutylamino)phenyl)-boronic acid 
• 32594-60-8 4-<4-(dibutylamino)phenyl>pyridine 

Relevant academic research and scientific papers

With near-infrared absorbing organic small molecule semiconductor material and its preparation and use

The present invention relates to a 2,2'-(2,8-bis(dialkyl amine)-indeno [1,2-b] fluorenes-6,12-diylidene)-dimalononitrile derivative as shown in a formula I, and a preparation method and use. The compound provided by the present invention as shown in the specification is a near-infrared absorbing organic small molecule semiconductor material, which can be used as an active layer of a bipolar organic field effect transistor, an active layer of a near-infrared light detector and other optoelectronic devices.

Unexpected Rearrangement of 2-Bromoaniline under Biphasic Alkylation Conditions

Alkylation of 2-bromoaniline with benzyl bromide under ostensibly basic N-alkylation conditions resulted in migration of bromine from the 2- to the 4-aryl position. Herein we report our studies to elucidate the mechanism of this rearrangement with the objective of suppressing this unexpected outcome. We find that careful choice of reagents is critical, and that this behavior may be extrapolated to alkylation reactions of electron-rich bromo- and iodoanilines in general.

Aerobic photooxidative bromination of aromatic compounds using carbon tetrabromide mediated by anthraquinone-2-carboxylic acid

We developed the aerobic photooxidative bromination of aromatic compounds using carbon tetrabromide in the presence of anthraquinone-2-carboxylic acid under visible light irradiation.

Nanoscale phase analysis of molecular cooperativity and thermal transitions in dendritic nonlinear optical glasses

A broad nanoscopic study of a wide-range of dendritic organic nonlinear optical (NLO) self-assembly molecular glasses reveals an intermediate thermal phase regime responsible for both enhanced electric field poling properties and strong phase stabilizatio

NEAR-INFRARED ABSORBING FILM COMPOSITIONS

A curable liquid formulation containing at least (i) one or more near-infrared absorbing triphenylamine -based dyes, and (ii) one or more casting solvents. The invention is also directed to solid near- infrared absorbing films composed of crosslinked forms of the curable liquid formulation. The invention is also directed to a microelectronic substrate containing a coating of the solid near-infrared absorbing film as well as a method for patterning a photoresist layer coated on a microelectronic substrate in the case where the near-infrared absorbing film is between the microelectronic substrate and a photoresist film.

NONLINEAR OPTICAL MATERIAL COMPOSITION AND METHOD OF MANUFACTURE

Embodiments of the present disclosure provide non-linear optical compounds and compositions comprising a silole-derivative. In an embodiment, the silole derivative comprises a chromophore including a structure represented by Formula (A): wherein each Of R

Synthesis of N-and C-trimethylsilyl-substituded anililes

N-Metallation of bromoanilines with ethylmagnesium bromide followed by a reaction with trimethylchlorosilane provided N-mono and N-bis(trimethylsilyl) bromoanilines depending on the structure of substrate. The metallation of bissilylated bromoanilines with butyllithium permitted the introduction of a trimethylsilyl substituent in the aromatic ring. Previously unknown 2-bromo-N,N-bis(trimethylsilyl)aniline, 2,6-dibromo-N-trimethylsilylaniline, 2,6-dibromo-N,N-bis(trimethylsilyl)aniline, 2-bromo-6-trimethylsilylaniline, 2-bromo-6-trimethylsilyl-N,N-bis(trimethylsilyl)aniline, 2-bromo-6- trimethylsilyl-N-trimethylsilylaniline, 2,4,6-tribromo-N-trimethylsilylaniline, and 2,4,6-tribromo-N,N-bis(trimethylsilyl)aniline were prepared. The structures of the compounds obtained were established by the chromato-mass spectrometry and 1H, 13C, and 29Si NMR spectroscopy.

Nonlinear optical compounds and methods for their preparation

Nonlinear optically active compounds, methods for making nonlinear optically active compounds, compounds useful for making nonlinear optically active compounds, methods for making compounds useful for making nonlinear optically active compounds, macrostructures that include nonlinear optically active components, and devices including the nonlinear optically active compounds and the macrostructures.

NONLINEAR OPTICAL COMPOUNDS AND METHODS FOR THEIR PREPARATION

Nonlinear optically active compounds, methods for making nonlinear optically active compounds, compounds useful for making nonlinear optically active compounds, methods for making compounds useful for making nonlinear optically active compounds, macrostructures tha tinclude nonlinear optically active components, and devices including the nonlinear optically active compounds and the macrostructures.

Synthesis and stability studies of conformationally locked 4-(diarylamino)aryl- and 4-(dialkylamino)phenyl-substituted second-order nonlinear optical polyene chromophores

A series of chromophores with high second-order nonlinearities has been synthesized; the chromphores consist of triarylamine or dialkylarylamine donors linked by a conformationally locked polyene bridge to a dicyanomethylidene acceptor. The use of bridges