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Catalog Number:
26264
CAS Number:
898289-06-0
Ester pinacol de l'acide 1-méthylindol-4-boronique
Purity:
≥ 95 % (HPLC)
Documents
$89.13 /100 mg
Taille
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Product Information

1-Methylindol-4-boronic acid pinacol ester is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valuable for its role in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in the development of pharmaceuticals and agrochemicals. Its unique structure, featuring a methylindole moiety, enhances its reactivity and compatibility with various substrates, making it an ideal choice for researchers looking to create complex molecular architectures.

In addition to its synthetic applications, 1-Methylindol-4-boronic acid pinacol ester has shown promise in the development of biologically active compounds, including potential anti-cancer agents. Its ability to facilitate the introduction of functional groups into indole derivatives opens new avenues for drug discovery and development. With its favorable properties and practical applications, this compound is a valuable addition to any research or industrial setting focused on innovative chemical synthesis.

CAS Number
898289-06-0
Purity
≥ 95 % (HPLC)
Molecular Formula
C 15 H 20 BNO 2
Molecular Weight
257.14
MDL Number
MFCD08690266
PubChem ID
18525785
Appearance
Blanc cassé uni
Conditions
Conserver à 0-8 °C
General Information
CAS Number
898289-06-0
Purity
≥ 95 % (HPLC)
Molecular Formula
C 15 H 20 BNO 2
Molecular Weight
257.14
MDL Number
MFCD08690266
PubChem ID
18525785
Appearance
Blanc cassé uni
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

1-Methylindol-4-boronic acid pinacol ester is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Medicinal Chemistry: It plays a crucial role in drug discovery, especially in the design of indole-based compounds, which are known for their biological activity against various diseases.
  • Material Science: The compound is used in creating advanced materials, including polymers and nanomaterials, enhancing properties like conductivity and strength.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential in diagnostics and therapeutic applications.
  • Fluorescent Probes: This chemical can be utilized in developing fluorescent probes for imaging applications, providing insights into biological processes at the cellular level.

Citations