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Catalog Number:
18004
CAS Number:
775351-30-9
Ácido 3-(2H-tetrazol-5-il)fenilborónico
Purity:
≥ 97 % (HPLC)
Documents
$168.35 /100 mg
Tamaño
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Product Information

3-(2H-Tetrazol-5-yl)phenyl-boronic acid is a versatile boronic acid derivative that plays a crucial role in various fields, particularly in medicinal chemistry and materials science. This compound is recognized for its unique ability to form reversible covalent bonds with diols, making it an essential building block in the synthesis of complex organic molecules. Its applications extend to the development of pharmaceuticals, where it serves as a key intermediate in the synthesis of biologically active compounds, including potential anti-cancer agents. Additionally, its utility in cross-coupling reactions, such as Suzuki-Miyaura coupling, highlights its importance in the formation of carbon-carbon bonds, facilitating the creation of diverse organic frameworks.

Researchers and industry professionals benefit from the compound's stability and reactivity, which allow for efficient functionalization and modification of various substrates. Its compatibility with a range of reaction conditions makes it a valuable tool in both academic research and industrial applications. With its potential to enhance the efficiency of synthetic pathways, 3-(2H-Tetrazol-5-yl)phenyl-boronic acid stands out as a significant contributor to advancements in chemical synthesis and drug discovery.

CAS Number
775351-30-9
Purity
≥ 97 % (HPLC)
Molecular Formula
C7H7BN4O2
Molecular Weight
189.97
MDL Number
MFCD06739100
PubChem ID
46737996
Appearance
Polvo blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
775351-30-9
Purity
≥ 97 % (HPLC)
Molecular Formula
C7H7BN4O2
Molecular Weight
189.97
MDL Number
MFCD06739100
PubChem ID
46737996
Appearance
Polvo blanquecino
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-(2H-Tetrazol-5-yl)phenyl-boronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in developing drugs that target specific biological pathways.
  • Bioconjugation: It is used in bioconjugation techniques to attach biomolecules to surfaces or other molecules, enhancing the effectiveness of diagnostics and therapeutics.
  • Material Science: The compound finds applications in creating advanced materials, such as sensors and catalysts, due to its unique chemical properties that facilitate reactions.
  • Organic Synthesis: It acts as a versatile building block in organic synthesis, allowing chemists to construct complex molecular architectures efficiently.
  • Research in Medicinal Chemistry: The compound is instrumental in medicinal chemistry research, helping scientists understand interactions at the molecular level and leading to the discovery of new therapeutic agents.

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