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Catalog Number:
40386
CAS Number:
62306-79-0
5-Methyl-2-furanboronic acid
Purity:
96 - 105% (Assay by titration)
Synonym(s):
5-Methyl-2-furylboronic acid
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Product Information

5-Methyl-2-furanboronic acid is a versatile boronic acid derivative that plays a significant role in organic synthesis and medicinal chemistry. This compound is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it invaluable for the formation of carbon-carbon bonds. Its unique furan ring structure enhances its reactivity and compatibility with various substrates, allowing for the development of complex molecules in pharmaceutical research. Additionally, 5-Methyl-2-furanboronic acid serves as a key intermediate in the synthesis of biologically active compounds, including potential drug candidates, thereby supporting advancements in therapeutic applications.

Researchers and industry professionals can leverage the properties of 5-Methyl-2-furanboronic acid for the development of novel materials and pharmaceuticals. Its ease of use in synthetic pathways and the ability to fine-tune molecular properties make it an attractive choice for those looking to innovate in chemical synthesis. With its growing relevance in the field, this compound stands out as a crucial tool for enhancing research outcomes and driving forward the development of new chemical entities.

Synonyms
5-Methyl-2-furylboronic acid
CAS Number
62306-79-0
Purity
96 - 105% (Assay by titration)
Molecular Formula
C5H7BO3
Molecular Weight
125.92
MDL Number
MFCD01114644
PubChem ID
2734372
Melting Point
82 °C (Lit.)
Appearance
White to light orange to green powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
5-Methyl-2-furylboronic acid
CAS Number
62306-79-0
Purity
96 - 105% (Assay by titration)
Molecular Formula
C5H7BO3
Molecular Weight
125.92
MDL Number
MFCD01114644
PubChem ID
2734372
Melting Point
82 °C (Lit.)
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

5-Methyl-2-furanboronic 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 plays a crucial role in Suzuki-Miyaura cross-coupling reactions, allowing chemists to create complex carbon-carbon bonds efficiently, which is essential in drug discovery.
  • Sensor Development: The unique properties of this boronic acid make it suitable for developing chemical sensors, particularly for detecting sugars and other biomolecules, enhancing biosensing technologies.
  • Material Science: It is utilized in the formulation of advanced materials, including polymers and coatings, due to its ability to modify the physical properties of materials, leading to improved performance.
  • Medicinal Chemistry: Researchers leverage its reactivity to design and optimize drug candidates, particularly in targeting specific biological pathways, which can lead to more effective treatments.

Citations