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Catalog Number:
40383
CAS Number:
13331-23-2
2-Furylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
Furan-2-boronic acid, 2-Furanylboronic acid
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Product Information

2-Furylboronic acid is a versatile organoboron compound recognized for its unique properties and applications in various fields, particularly in organic synthesis and medicinal chemistry. This compound features a furan ring, which enhances its reactivity and makes it an excellent candidate for cross-coupling reactions, such as Suzuki-Miyaura coupling. Researchers and industry professionals utilize 2-Furylboronic acid for the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals, due to its ability to form stable complexes with various substrates. Its distinctive structure allows for selective functionalization, making it a valuable tool in the development of novel compounds.

In addition to its synthetic applications, 2-Furylboronic acid has shown potential in the field of materials science, where it can be employed in the creation of advanced materials with tailored properties. Its compatibility with various reaction conditions and ease of handling further enhance its appeal for laboratory and industrial use. Whether you are involved in drug discovery or materials development, 2-Furylboronic acid offers significant advantages, including improved yields and selectivity in reactions, making it an essential addition to your chemical toolkit.

Synonyms
Furan-2-boronic acid, 2-Furanylboronic acid
CAS Number
13331-23-2
Purity
95 - 105% (Assay by titration)
Molecular Formula
C4H5BO3
Molecular Weight
111.89
MDL Number
MFCD00799544
PubChem ID
2734357
Melting Point
112 °C (dec.)
Appearance
White to slightly yellow crystalline powd
Conditions
Store at ≤ -4 °C
General Information
Synonyms
Furan-2-boronic acid, 2-Furanylboronic acid
CAS Number
13331-23-2
Purity
95 - 105% (Assay by titration)
Molecular Formula
C4H5BO3
Molecular Weight
111.89
MDL Number
MFCD00799544
PubChem ID
2734357
Melting Point
112 °C (dec.)
Appearance
White to slightly yellow crystalline powd
Conditions
Store at ≤ -4 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Furylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds, making it valuable in the production of complex organic compounds.
  • Sensor Development: 2-Furylboronic acid is employed in the creation of chemical sensors for detecting glucose and other biomolecules, enhancing diagnostics in the medical field.
  • Polymer Chemistry: This compound can be incorporated into polymer matrices, improving material properties for applications in coatings and adhesives.
  • Research in Catalysis: It plays a role in catalytic processes, contributing to more efficient and sustainable chemical reactions in various industrial applications.

Citations