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Catalog Number:
26375
CAS Number:
796851-30-4
Éster de pinacol del ácido benzofurano-3-borónico
Purity:
≥ 95 % (HPLC)
Synonym(s):
1-(benzofuran-3-il)-3,3,4,4-tetrametilborolano
Documents
$142.81 /100 mg
Tamaño
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Product Information

Benzofuran-3-boronic acid pinacol ester is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic ester 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 incorporation into various synthetic pathways.

In addition to its synthetic applications, Benzofuran-3-boronic acid pinacol ester has shown potential in the development of fluorescent probes and sensors, enhancing its relevance in analytical chemistry. Its compatibility with diverse functional groups and its ability to undergo further transformations make it an attractive option for chemists looking to innovate in their research. With its broad applicability and unique properties, this compound stands out as a valuable resource for professionals in the fields of chemistry and materials science.

Synonyms
1-(benzofuran-3-il)-3,3,4,4-tetrametilborolano
CAS Number
796851-30-4
Purity
≥ 95 % (HPLC)
Molecular Formula
C 14 H 17 BO 3
Molecular Weight
244.1
MDL Number
MFCD11841067
PubChem ID
43811031
Appearance
Sólido de color blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
1-(benzofuran-3-il)-3,3,4,4-tetrametilborolano
CAS Number
796851-30-4
Purity
≥ 95 % (HPLC)
Molecular Formula
C 14 H 17 BO 3
Molecular Weight
244.1
MDL Number
MFCD11841067
PubChem ID
43811031
Appearance
Sólido de color 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

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

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Medicinal Chemistry: It plays a crucial role in drug discovery, where it is used to create compounds with potential therapeutic effects, especially in targeting specific diseases.
  • Material Science: The compound is employed in the development of advanced materials, including polymers and nanomaterials, enhancing properties like strength and conductivity.
  • Fluorescent Probes: It is utilized in the creation of fluorescent probes for biological imaging, allowing researchers to visualize cellular processes in real-time.
  • Cross-Coupling Reactions: This chemical is vital in Suzuki-Miyaura coupling reactions, facilitating the formation of carbon-carbon bonds, which is essential in various synthetic pathways.

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