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Catalog Number:
24740
CAS Number:
1245816-10-7
5-Methyl-1H-indazole-4-boronic acid        
Purity:
≥ 95% (Assay)
Documents
$79.22 /250MG
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Product Information

5-Methyl-1H-indazole-4-boronic acid is a versatile boronic acid derivative that plays a crucial role in various chemical synthesis processes. This compound is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block in the development of pharmaceuticals and agrochemicals. Its unique structure allows for the formation of complex organic molecules, which are vital in drug discovery and development. Researchers appreciate its stability and reactivity, which facilitate the creation of diverse compounds with potential therapeutic applications.

In addition to its significance in organic synthesis, 5-Methyl-1H-indazole-4-boronic acid is also utilized in the development of sensors and materials science, where its boronic acid functionality can interact with diols, enabling the design of responsive materials. This compound's ability to form stable complexes with various substrates enhances its utility in various fields, including medicinal chemistry and materials engineering. Its practical applications and unique properties make it a valuable asset for researchers and industry professionals seeking innovative solutions.

CAS Number
1245816-10-7
Purity
≥ 95% (Assay)
Molecular Formula
C8H9BN2O2
Molecular Weight
175.98
MDL Number
MFCD10001490
PubChem ID
44119475
Appearance
White to light yellow powder
Conditions
Store at 0-8 °C
General Information
CAS Number
1245816-10-7
Purity
≥ 95% (Assay)
Molecular Formula
C8H9BN2O2
Molecular Weight
175.98
MDL Number
MFCD10001490
PubChem ID
44119475
Appearance
White to light yellow powder
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

5-Methyl-1H-indazole-4-boronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer agents, due to its ability to inhibit specific enzymes involved in tumor growth.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing for the attachment of biomolecules to surfaces or other molecules, which is essential in creating targeted drug delivery systems.
  • Material Science: The compound is used in the development of advanced materials, such as sensors and catalysts, benefiting from its unique electronic properties that enhance performance in various applications.
  • Organic Synthesis: As a boronic acid derivative, it plays a crucial role in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds in organic synthesis, which is vital for creating complex organic molecules.
  • Research in Agrochemicals: It is also being explored in the agrochemical industry for the development of new herbicides and pesticides, offering potential advantages in crop protection and yield improvement.

Citations