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Boronic acid, B-[4-(1-naphthalenyl-2-naphthalenylamino)phenyl]-
  • Chemical Name: Boronic acid, B-[4-(1-naphthalenyl-2-naphthalenylamino)phenyl]-
  • CAS No.: 1232101-98-2

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What is the Boronic acid, B-[4-(1-naphthalenyl-2-naphthalenylamino)phenyl]- ?

Boronic acid, B-[4-(1-naphthalenyl-2-naphthalenylamino)phenyl]- is , while it's Molecular Formula is C26H20BNO2. Used in Organic Synthesis:
Boronic acid, B-[4-(1-naphthalenyl-2-naphthalenylamino)phenyl]-, is used as a reagent in organic synthesis for its ability to form boronate esters with diols, facilitating the formation of new carbon-carbon or carbon-heteroatom bonds. This reactivity allows for the synthesis of complex organic molecules and the modification of existing compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, Boronic acid, B-[4-(1-naphthalenyl-2-naphthalenylamino)phenyl]-, is utilized as a building block for the development of novel pharmaceutical compounds. Its unique structure and reactivity can be leveraged to design and synthesize new drugs with improved potency, selectivity, and pharmacokinetic properties.
Used in Materials Science:
Boronic acid, B-[4-(1-naphthalenyl-2-naphthalenylamino)phenyl]-, is employed in materials science for the development of advanced materials with tailored properties. Boronic acid, B-[4-(1-naphthalenyl-2-naphthalenylamino)phenyl]-'s reactivity and structural features can be exploited to create new materials with applications in areas such as sensors, catalysts, and functional coatings.
Used in Chemical Sensors:
Boronic acid, B-[4-(1-naphthalenyl-2-naphthalenylamino)phenyl]-, is used as a sensing element in chemical sensors for its ability to selectively recognize and bind to specific analytes, such as sugars or other diols. The formation of boronate esters upon interaction with the target analyte can lead to a measurable change in the sensor's properties, enabling the detection and quantification of the analyte in various samples.
Used in Catalyst Design:
In the design of catalysts, Boronic acid, B-[4-(1-naphthalenyl-2-naphthalenylamino)phenyl]-, is utilized as a catalyst component or ligand, taking advantage of its reactivity and structural features to enhance the catalytic activity and selectivity of the catalyst system. This can lead to more efficient and environmentally friendly catalytic processes in various chemical reactions.
Used in Functional Coatings:
Boronic acid, B-[4-(1-naphthalenyl-2-naphthalenylamino)phenyl]-, is incorporated into functional coatings for its ability to form reversible covalent bonds with substrates containing diols or other nucleophiles. This property can be used to create coatings with enhanced adhesion, self-healing capabilities, or stimuli-responsive behavior, finding applications in various industries such as automotive, aerospace, and electronics.

How to get the best price on Boronic acid, B-[4-(1-naphthalenyl-2-naphthalenylamino)phenyl]-?

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