Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
19162
CAS Number:
861905-87-5, 937049-58-6
1H-Indazole-6-boronic acid pinacol ester
Purity:
≥ 95% (HPLC)
Synonym(s):
6-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-indazole
Documents
$74.81 /250MG
Pack Size Availability Price
Request Bulk Quote
Product Information

1H-Indazole-6-boronic acid pinacol ester is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized 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 enhances its applicability in various laboratory settings.

In addition to its synthetic utility, 1H-Indazole-6-boronic acid pinacol ester has shown potential in the development of targeted therapies, particularly in oncology, where boron-containing compounds are being explored for their therapeutic effects. Its favorable properties, such as solubility and reactivity, position it as a valuable reagent for chemists looking to innovate in drug design and development. With its broad range of applications, this compound is an indispensable tool for professionals aiming to push the boundaries of chemical research and development.

Synonyms
6-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-indazole
CAS Number
861905-87-5, 937049-58-6
Purity
≥ 95% (HPLC)
Molecular Formula
C13H17BN2O2
Molecular Weight
244.1
MDL Number
MFCD07368067
Appearance
White solid
Conditions
Store at 0-8 °C
General Information
Synonyms
6-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-indazole
CAS Number
861905-87-5, 937049-58-6
Purity
≥ 95% (HPLC)
Molecular Formula
C13H17BN2O2
Molecular Weight
244.1
MDL Number
MFCD07368067
Appearance
White solid
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

1H-Indazole-6-boronic acid pinacol ester is widely utilized in research focused on:

  • Medicinal Chemistry: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in developing targeted cancer therapies due to its ability to form stable complexes with biological targets.
  • Organic Synthesis: It is employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, which allows for the formation of carbon-carbon bonds, essential in creating complex organic molecules.
  • Material Science: The compound is used in the development of advanced materials, including polymers and nanomaterials, enhancing properties like conductivity and strength.
  • Agricultural Chemistry: It plays a role in creating agrochemicals, contributing to the development of more effective herbicides and pesticides that are environmentally friendly.
  • Bioconjugation: This chemical is useful in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in diagnostics and therapeutic applications.

Citations