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Catalog Number:
26365
CAS Number:
1204580-79-9
2-Methylindazole-6-boronic acid pinacol ester
Purity:
≥ 95% (HPLC)
Synonym(s):
2-Methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole
Documents
$86.23 /250MG
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Product Information

2-Methylindazole-6-boronic acid pinacol ester is a versatile compound that plays a significant role in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its utility in Suzuki-Miyaura cross-coupling reactions, which are essential for the formation of carbon-carbon bonds. Its unique structure allows for the introduction of various functional groups, making it an invaluable tool for researchers aiming to develop new pharmaceuticals and agrochemicals. The compound's stability and reactivity under mild conditions enhance its appeal in synthetic pathways, providing a reliable option for chemists looking to streamline their processes.

In addition to its synthetic applications, 2-Methylindazole-6-boronic acid pinacol ester has shown promise in the development of biologically active molecules, particularly in the field of cancer research. Its ability to facilitate the construction of complex molecular architectures positions it as a key player in the design of novel therapeutic agents. Researchers and industry professionals can benefit from its efficiency and effectiveness in various applications, making it a valuable addition to any chemical toolkit.

Synonyms
2-Methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole
CAS Number
1204580-79-9
Purity
≥ 95% (HPLC)
Molecular Formula
C14H19BN2O2
Molecular Weight
258.13
MDL Number
MFCD11109435
PubChem ID
44118252
Appearance
White solid
Conditions
Store at 0-8°C
General Information
Synonyms
2-Methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole
CAS Number
1204580-79-9
Purity
≥ 95% (HPLC)
Molecular Formula
C14H19BN2O2
Molecular Weight
258.13
MDL Number
MFCD11109435
PubChem ID
44118252
Appearance
White solid
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Methylindazole-6-boronic acid pinacol ester is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in developing new drugs for treating cancer and other diseases.
  • Chemical Synthesis: It is employed in cross-coupling reactions, which are essential for creating complex organic molecules, making it invaluable in organic chemistry laboratories.
  • Material Science: The compound is used in the development of advanced materials, including polymers and nanomaterials, enhancing their properties for applications in electronics and coatings.
  • Bioconjugation: It plays a role in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is crucial for drug delivery systems and diagnostics.
  • Research in Catalysis: This compound is utilized in catalysis research, contributing to the development of more efficient and selective catalytic processes, which can lead to greener chemical manufacturing.

Citations