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Catalog Number:
40350
CAS Number:
669072-93-9
9-Ethylcarbazole-3-boronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
9-Ethyl-3-carbazole boronic acid
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Product Information

9-Ethylcarbazole-3-boronic acid is a versatile compound that plays a significant role in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it a valuable building block for the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure allows for the formation of carbon-carbon bonds, which is essential in the creation of various functionalized compounds.

In addition to its synthetic utility, 9-Ethylcarbazole-3-boronic acid exhibits potential applications in the field of materials science, particularly in the development of organic light-emitting diodes (OLEDs) and organic photovoltaics. Researchers appreciate its stability and reactivity, which can lead to innovative solutions in electronic materials. With its diverse applications and the ability to enhance the efficiency of chemical reactions, this compound is an excellent choice for professionals seeking to advance their research or product development in organic synthesis and materials innovation.

Synonyms
9-Ethyl-3-carbazole boronic acid
CAS Number
669072-93-9
Purity
97 - 105% (Assay by titration)
Molecular Formula
C14H14BNO2
Molecular Weight
239.08
MDL Number
MFCD09743121
PubChem ID
45382262
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
9-Ethyl-3-carbazole boronic acid
CAS Number
669072-93-9
Purity
97 - 105% (Assay by titration)
Molecular Formula
C14H14BNO2
Molecular Weight
239.08
MDL Number
MFCD09743121
PubChem ID
45382262
Appearance
White to off-white crystalline powder
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-Ethylcarbazole-3-boronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Materials Science: It is employed in the fabrication of advanced materials, including organic light-emitting diodes (OLEDs), due to its excellent electronic properties.
  • Chemical Sensors: The compound is used in the creation of chemical sensors that can detect specific analytes, enhancing safety and monitoring in industrial applications.
  • Bioconjugation: It plays a role in bioconjugation techniques, allowing for the attachment of biomolecules to surfaces or other molecules, which is crucial in drug delivery systems.
  • Research in Catalysis: This chemical is investigated for its potential in catalytic processes, offering advantages in reaction efficiency and selectivity compared to traditional catalysts.

Citations