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Catalog Number:
26367
CAS Number:
885698-95-3
2-Methylindazole-4-boronic acid pinacol ester
Purity:
≥ 95% (HPLC)
Synonym(s):
2-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole
Documents
$96.34 /100MG
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Product Information

2-Methylindazole-4-boronic acid pinacol ester is a versatile compound that plays a significant role in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the development of complex organic molecules. Its unique structure allows for the formation of carbon-carbon bonds, which is crucial in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Researchers appreciate its stability and ease of handling, which facilitate its use in various laboratory applications.

In addition to its synthetic utility, 2-Methylindazole-4-boronic acid pinacol ester has shown promise in the development of biologically active compounds. Its incorporation into drug discovery processes can lead to the identification of novel therapeutic agents, particularly in the fields of oncology and infectious diseases. The compound's favorable properties, such as solubility and reactivity, enhance its applicability in diverse research settings, making it a valuable asset for chemists and industry professionals alike.

Synonyms
2-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole
CAS Number
885698-95-3
Purity
≥ 95% (HPLC)
Molecular Formula
C14H19BN2O2
Molecular Weight
258.13
MDL Number
MFCD11109437
PubChem ID
44118254
Appearance
White solid
Conditions
Store at 0-8°C
General Information
Synonyms
2-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole
CAS Number
885698-95-3
Purity
≥ 95% (HPLC)
Molecular Formula
C14H19BN2O2
Molecular Weight
258.13
MDL Number
MFCD11109437
PubChem ID
44118254
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-4-boronic acid pinacol ester is widely utilized in research focused on:

  • Drug Development: This compound serves as a crucial building block in the synthesis of pharmaceuticals, particularly in developing new anti-cancer agents due to its ability to form stable complexes with biological targets.
  • Organic Synthesis: It is employed in various organic reactions, including Suzuki-Miyaura cross-coupling, which is essential for creating complex organic molecules used in agrochemicals and fine chemicals.
  • Material Science: The compound is utilized in the development of advanced materials, such as conductive polymers and organic light-emitting diodes (OLEDs), enhancing the performance of electronic devices.
  • Bioconjugation: Its unique boronic acid functionality allows for selective binding to diols in biomolecules, making it valuable for creating targeted drug delivery systems in biomedicine.
  • Analytical Chemistry: The compound is used as a reagent in various analytical techniques, aiding in the detection and quantification of specific biomolecules, which is crucial for research in diagnostics.

Citations