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Catalog Number:
40015
CAS Number:
269410-24-4
5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
Purity:
≥ 98% (GC)
Synonym(s):
5-Indoleboronic acid pinacol ester
Documents
$148.22 /1G
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Product Information

5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole is a versatile compound known for its unique boron-containing structure, which enhances its reactivity and stability in various chemical reactions. This compound is particularly valuable in organic synthesis and medicinal chemistry, where it serves as a key intermediate in the development of pharmaceuticals and agrochemicals. Its ability to participate in cross-coupling reactions makes it an essential building block for creating complex molecular architectures, which are crucial in drug discovery and development.

Researchers and industry professionals benefit from its high selectivity and efficiency in reactions, allowing for streamlined processes in the synthesis of indole derivatives. The compound's stability under various conditions also makes it suitable for use in diverse applications, including materials science and catalysis. With its unique properties, 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole stands out as a valuable tool for advancing research and innovation in multiple fields.

Synonyms
5-Indoleboronic acid pinacol ester
CAS Number
269410-24-4
Purity
≥ 98% (GC)
Molecular Formula
C14H18BNO2
Molecular Weight
243.11
MDL Number
MFCD03789263
PubChem ID
2734772
Melting Point
124 - 128 °C
Appearance
White to off-white crystalline powder
Conditions
Store at ≤ -10 °C
General Information
Synonyms
5-Indoleboronic acid pinacol ester
CAS Number
269410-24-4
Purity
≥ 98% (GC)
Molecular Formula
C14H18BNO2
Molecular Weight
243.11
MDL Number
MFCD03789263
PubChem ID
2734772
Melting Point
124 - 128 °C
Appearance
White to off-white crystalline powder
Conditions
Store at ≤ -10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in organic chemistry, facilitating the synthesis of complex molecules. Its unique structure allows for efficient reactions, making it valuable for researchers developing new compounds.
  • Pharmaceutical Development: In the pharmaceutical industry, it is used to create indole derivatives, which are important in drug discovery. These derivatives often exhibit biological activity, aiding in the development of new therapeutic agents.
  • Material Science: The compound is employed in the creation of advanced materials, such as polymers and coatings. Its properties enhance the performance of these materials, making them suitable for various industrial applications.
  • Fluorescent Probes: It can be utilized in the development of fluorescent probes for biological imaging. Researchers can track cellular processes with high precision, benefiting fields like biochemistry and molecular biology.
  • Catalysis: This chemical is also explored as a catalyst in various chemical reactions. Its efficiency can lead to faster reaction rates and improved yields, providing a significant advantage in industrial processes.

Citations