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Catalog Number:
30969
CAS Number:
419536-33-7
4-(9H-Carbazol-9-yl)phenylboronic acid (contains varying amounts of Anhydride)
Purity:
≥ 97% (HPLC)
Synonym(s):
4-(9H-Carbazol-9-yl)benzeneboronic acid (contains varying amounts of anhydride)
Documents
$107.86 /1G
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Product Information

4-(9H-Carbazol-9-yl)phenylboronic acid is a versatile compound known for its unique properties that make it invaluable in various research and industrial applications. This boronic acid derivative is particularly recognized for its role in Suzuki-Miyaura cross-coupling reactions, which are essential in the synthesis of complex organic molecules, including pharmaceuticals and advanced materials. Its ability to form stable complexes with diols enhances its utility in sensor technology, where it is employed for the detection of sugars and other biomolecules.

Additionally, this compound exhibits significant potential in organic electronics, particularly in the development of organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs), where its electronic properties can be harnessed to improve device efficiency. Researchers appreciate its ease of handling and compatibility with various substrates, making it a preferred choice in both academic and industrial settings. With its broad applicability and effectiveness, 4-(9H-Carbazol-9-yl)phenylboronic acid stands out as a key ingredient for innovative solutions in synthetic chemistry and materials science.

Synonyms
4-(9H-Carbazol-9-yl)benzeneboronic acid (contains varying amounts of anhydride)
CAS Number
419536-33-7
Purity
≥ 97% (HPLC)
Molecular Formula
C18H14BNO2
Molecular Weight
287.13
MDL Number
MFCD13176534
PubChem ID
23120827
Melting Point
264 °C
Appearance
White to almost white crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
4-(9H-Carbazol-9-yl)benzeneboronic acid (contains varying amounts of anhydride)
CAS Number
419536-33-7
Purity
≥ 97% (HPLC)
Molecular Formula
C18H14BNO2
Molecular Weight
287.13
MDL Number
MFCD13176534
PubChem ID
23120827
Melting Point
264 °C
Appearance
White to almost white crystalline powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-(9H-Carbazol-9-yl)phenylboronic acid is widely utilized in research focused on:

  • Organic Electronics: This compound plays a crucial role in the development of organic light-emitting diodes (OLEDs) and organic photovoltaic cells, enhancing efficiency and stability in these devices.
  • Medicinal Chemistry: It serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in developing targeted cancer therapies due to its ability to interact with specific biological targets.
  • Sensor Technology: The compound is used in the fabrication of chemical sensors, where its boronic acid functionality allows for selective detection of sugars and other biomolecules, making it valuable in biomedical applications.
  • Polymer Chemistry: It is incorporated into polymer matrices to improve mechanical properties and thermal stability, which is beneficial for creating advanced materials in industries such as automotive and aerospace.
  • Research in Supramolecular Chemistry: The compound's unique structure enables the formation of complex molecular assemblies, aiding in the study of molecular recognition processes and the development of new materials with tailored properties.

Citations