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Catalog Number:
17467
CAS Number:
374715-22-7
3-Phenylisoxazole-5-boronic acid pinacol ester
Purity:
≥ 95% (NMR)
Synonym(s):
(3-Phenylisoxazol-5-yl)boronic acid pinacol ester
Documents
$127.79 /25MG
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Product Information

3-Phenylisoxazole-5-boronic acid pinacol ester is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic ester is particularly valued for its role in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in the development of complex organic molecules. Its unique structure, featuring both a phenyl group and a boronic acid moiety, enhances its reactivity and selectivity, making it an ideal candidate for the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Researchers appreciate its stability and ease of handling, which facilitate its application in various synthetic pathways.

In addition to its synthetic utility, 3-Phenylisoxazole-5-boronic acid pinacol ester has shown potential in the development of novel therapeutic agents. Its ability to act as a building block in the creation of isoxazole-containing compounds opens avenues for the exploration of new drug candidates targeting various diseases. With its favorable properties and broad applicability, this compound stands out as a valuable tool for chemists and researchers aiming to innovate in their respective fields.

Synonyms
(3-Phenylisoxazol-5-yl)boronic acid pinacol ester
CAS Number
374715-22-7
Purity
≥ 95% (NMR)
Molecular Formula
C15H18BNO3
Molecular Weight
271.12
MDL Number
MFCD09878915
PubChem ID
44668373
Appearance
Light brown solid
Conditions
Store at 0-8 °C
General Information
Synonyms
(3-Phenylisoxazol-5-yl)boronic acid pinacol ester
CAS Number
374715-22-7
Purity
≥ 95% (NMR)
Molecular Formula
C15H18BNO3
Molecular Weight
271.12
MDL Number
MFCD09878915
PubChem ID
44668373
Appearance
Light brown 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

3-Phenylisoxazole-5-boronic acid pinacol ester is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key intermediate in the synthesis of various organic molecules, making it valuable for chemists developing new pharmaceuticals and agrochemicals.
  • Medicinal Chemistry: It is used in the design and development of novel drugs, particularly in targeting specific biological pathways, which can lead to more effective treatments with fewer side effects.
  • Material Science: The compound is applied in creating advanced materials, such as polymers and nanomaterials, enhancing properties like strength and durability for industrial applications.
  • Fluorescent Probes: It functions as a fluorescent probe in biological imaging, allowing researchers to visualize cellular processes in real-time, which is crucial for understanding disease mechanisms.
  • Catalysis: This chemical is utilized in catalytic processes, improving reaction efficiency and selectivity, which is essential for sustainable chemical manufacturing practices.

Citations