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Catalog Number:
40382
CAS Number:
55552-70-0
3-Furylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
Furan-3-boronic acid, 3-Furanylboronic acid
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Product Information

3-Furylboronic acid is a versatile organoboron compound that plays a significant role in organic synthesis and medicinal chemistry. Known for its unique reactivity, this compound is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in the synthesis of complex organic molecules. Researchers and industry professionals utilize 3-Furylboronic acid to create a variety of biologically active compounds, including pharmaceuticals and agrochemicals, due to its ability to introduce the furan moiety, which is often associated with enhanced biological activity.

Additionally, 3-Furylboronic acid exhibits excellent solubility in polar solvents, making it an ideal candidate for various applications in both laboratory and industrial settings. Its stability and ease of handling further enhance its appeal for researchers looking to streamline their synthetic processes. With its potential to facilitate the development of new materials and drug candidates, 3-Furylboronic acid stands out as a crucial building block in modern chemistry.

Synonyms
Furan-3-boronic acid, 3-Furanylboronic acid
CAS Number
55552-70-0
Purity
95 - 105% (Assay by titration)
Molecular Formula
C4H5BO3
Molecular Weight
111.89
MDL Number
MFCD01319007
PubChem ID
2734358
Melting Point
139 - 144 °C
Appearance
White to light orange to green powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
Furan-3-boronic acid, 3-Furanylboronic acid
CAS Number
55552-70-0
Purity
95 - 105% (Assay by titration)
Molecular Formula
C4H5BO3
Molecular Weight
111.89
MDL Number
MFCD01319007
PubChem ID
2734358
Melting Point
139 - 144 °C
Appearance
White to light orange to green powder
Conditions
Store at 2 - 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-Furylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: It serves as a key building block in the synthesis of various organic compounds, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: This compound is essential in Suzuki-Miyaura coupling reactions, allowing for the formation of carbon-carbon bonds, which is crucial in creating complex molecules.
  • Fluorescent Probes: It is used in the design of fluorescent probes for biological imaging, enhancing the ability to visualize cellular processes in real-time.
  • Sensor Development: 3-Furylboronic acid is applied in the creation of sensors for detecting sugars and other biomolecules, which is valuable in food safety and medical diagnostics.
  • Material Science: Its properties make it suitable for developing advanced materials, including polymers and nanocomposites, that have applications in electronics and packaging.

Citations