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Catalog Number:
26133
CAS Number:
191162-40-0
Ácido N -metilindol-2-borónico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ácido 1-metil- 1H- indol-2-borónico
Documents
$74.81 /100 mg
Tamaño
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Product Information

N-Methylindole-2-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 unique ability to form reversible covalent bonds with diols, making it an essential building block in the development of various pharmaceuticals and agrochemicals. Its applications extend to the synthesis of biologically active molecules, where it serves as a key intermediate in the preparation of potent inhibitors and other therapeutic agents. Researchers appreciate its utility in Suzuki-Miyaura cross-coupling reactions, which are pivotal in constructing complex organic frameworks.

In addition to its synthetic applications, N-Methylindole-2-boronic acid has shown promise in the field of materials science, particularly in the development of sensors and catalysts. Its ability to interact with various substrates enhances its functionality in creating innovative solutions for environmental monitoring and chemical detection. With its favorable properties and broad applicability, N-Methylindole-2-boronic acid stands out as a valuable resource for researchers and industry professionals seeking to advance their projects in organic synthesis and beyond.

Synonyms
Ácido 1-metil- 1H- indol-2-borónico
CAS Number
191162-40-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C9H10BNO2
Molecular Weight
174.99
MDL Number
MFCD01114668
PubChem ID
22733820
Melting Point
130-136 ?C
Appearance
Sólido blanco
Conditions
Conservar a ≤ -4 °C
General Information
Synonyms
Ácido 1-metil- 1H- indol-2-borónico
CAS Number
191162-40-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C9H10BNO2
Molecular Weight
174.99
MDL Number
MFCD01114668
PubChem ID
22733820
Melting Point
130-136 ?C
Appearance
Sólido blanco
Conditions
Conservar a ≤ -4 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

N-Methylindole-2-boronic acid 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 is used in drug discovery processes, especially for creating compounds that target specific biological pathways, enhancing the efficacy of therapeutic agents.
  • Bioconjugation: The boronic acid functionality allows for selective binding to diols, making it valuable in creating bioconjugates for targeted drug delivery systems.
  • Fluorescent Probes: It can be incorporated into fluorescent probes for biological imaging, aiding researchers in visualizing cellular processes in real-time.
  • Material Science: This compound is explored in the development of new materials, such as sensors and catalysts, due to its unique electronic properties.

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