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Catalog Number:
30959
CAS Number:
854952-58-2
9-Phenylcarbazole-3-boronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
9-Phenyl-9H-carbazole-3-boronic acid, N-Phenyl-3-carbazoleboronic acid
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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
9-Phenyl-9H-carbazole-3-boronic acid, N-Phenyl-3-carbazoleboronic acid
CAS Number
854952-58-2
Purity
97 - 105% (Assay by titration)
Molecular Formula
C18H14BNO2
Molecular Weight
287.13
MDL Number
MFCD12196936
PubChem ID
51358450
Appearance
White to slightly yellow crystalline powd
Conditions
Store at RT
General Information
Synonyms
9-Phenyl-9H-carbazole-3-boronic acid, N-Phenyl-3-carbazoleboronic acid
CAS Number
854952-58-2
Purity
97 - 105% (Assay by titration)
Molecular Formula
C18H14BNO2
Molecular Weight
287.13
MDL Number
MFCD12196936
PubChem ID
51358450
Appearance
White to slightly yellow crystalline powd
Conditions
Store at 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.

Citations