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Catalog Number:
17605
CAS Number:
338454-14-1
1H-Indazole-5-boronic acid
Purity:
≥ 95% (HPLC)
Synonym(s):
1H-Indazol-5-yl-5-boronic acid
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$58.39 /250MG
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Product Information

1H-Indazole-5-boronic acid is a versatile compound recognized for its significant role in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Researchers and industry professionals utilize this compound in the development of pharmaceuticals, agrochemicals, and advanced materials. Its unique properties enable the synthesis of complex molecules, facilitating the creation of innovative compounds with potential therapeutic applications.

Additionally, 1H-Indazole-5-boronic acid has garnered attention for its potential in the development of targeted therapies, particularly in oncology, where it may play a role in the design of selective inhibitors. Its compatibility with various functional groups enhances its utility in diverse chemical environments, allowing for greater flexibility in synthetic pathways. With its proven efficacy and broad applicability, this compound stands out as a valuable tool for researchers aiming to push the boundaries of chemical innovation.

Synonyms
1H-Indazol-5-yl-5-boronic acid
CAS Number
338454-14-1
Purity
≥ 95% (HPLC)
Molecular Formula
C7H7BN2O2
Molecular Weight
161.96
MDL Number
MFCD06739151
PubChem ID
17750504
Appearance
White to off-white solid
Conditions
Store at 0-8 °C
General Information
Synonyms
1H-Indazol-5-yl-5-boronic acid
CAS Number
338454-14-1
Purity
≥ 95% (HPLC)
Molecular Formula
C7H7BN2O2
Molecular Weight
161.96
MDL Number
MFCD06739151
PubChem ID
17750504
Appearance
White to off-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-5-boronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a crucial building block in the synthesis of various pharmaceutical agents, particularly in the development of anti-cancer drugs. Its boronic acid functionality allows for effective interactions with biological targets.
  • Chemical Synthesis: It is employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, which are essential for forming carbon-carbon bonds in organic synthesis, making it valuable in creating complex organic molecules.
  • Material Science: The compound is used in the development of advanced materials, including polymers and nanomaterials, where its unique properties can enhance material performance, such as conductivity and mechanical strength.
  • Bioconjugation: It plays a role in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is critical in the development of biosensors and targeted drug delivery systems.
  • Analytical Chemistry: This chemical is utilized in various analytical methods, including chromatography and mass spectrometry, to improve the detection and quantification of specific compounds in complex mixtures.