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Catalog Number:
30959
CAS Number:
854952-58-2
Ácido 9-fenilcarbazol-3-borónico
Purity:
97 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 9-fenil-9 H -carbazol-3-borónico, Ácido N -fenil-3-carbazolborónico
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$264.60 /5G
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Product Information

9-Phenylcarbazole-3-boronic acid is a versatile compound recognized for its unique properties and applications in organic synthesis and materials science. This boronic acid derivative is particularly valued in the development of organic light-emitting diodes (OLEDs) and organic photovoltaics, where it serves as a key building block for efficient charge transport materials. Its ability to form stable complexes with diols makes it an essential reagent in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds in the synthesis of complex organic molecules.

Researchers and industry professionals appreciate 9-Phenylcarbazole-3-boronic acid for its high thermal stability and excellent solubility in organic solvents, which enhance its usability in various chemical processes. Its distinctive structure allows for the fine-tuning of electronic properties, making it ideal for applications in optoelectronic devices. With its growing importance in the fields of organic electronics and medicinal chemistry, this compound stands out as a valuable asset for innovative research and development projects.

Synonyms
Ácido 9-fenil-9 H -carbazol-3-borónico, Ácido N -fenil-3-carbazolborónico
CAS Number
854952-58-2
Purity
97 - 105% (Ensayo por titulación)
Molecular Formula
C18H14BNO2
Molecular Weight
287.13
MDL Number
MFCD12196936
PubChem ID
51358450
Appearance
Polvo cristalino de color blanco a ligeramente amarillo.
Conditions
Tienda en RT
General Information
Synonyms
Ácido 9-fenil-9 H -carbazol-3-borónico, Ácido N -fenil-3-carbazolborónico
CAS Number
854952-58-2
Purity
97 - 105% (Ensayo por titulación)
Molecular Formula
C18H14BNO2
Molecular Weight
287.13
MDL Number
MFCD12196936
PubChem ID
51358450
Appearance
Polvo cristalino de color blanco a ligeramente amarillo.
Conditions
Tienda en RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

9-Phenylcarbazole-3-boronic acid is widely utilized in research focused on:

  • Organic Electronics: This compound is used in the development of organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs), enhancing device efficiency and stability.
  • Medicinal Chemistry: It serves as a key intermediate in the synthesis of pharmaceuticals, particularly in developing anti-cancer agents, due to its ability to interact with biological targets.
  • Sensor Technology: The compound is applied in creating sensors for detecting biomolecules, leveraging its boronic acid functionality to selectively bind with glucose and other sugars.
  • Polymer Chemistry: It is incorporated into polymer matrices to improve mechanical properties and thermal stability, making it valuable for producing high-performance materials.
  • Catalysis: This chemical acts as a catalyst in various organic reactions, facilitating processes such as Suzuki coupling, which is essential for forming carbon-carbon bonds in complex organic molecules.

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