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Catalog Number:
40357
CAS Number:
162607-20-7
5-Methyl-2-thiopheneboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
5-Methylthiophene-2-boronic acid
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Product Information

5-Methyl-2-thiopheneboronic acid is a versatile organoboron compound that plays a crucial role in various chemical synthesis processes. This compound is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential reagent in the development of pharmaceuticals and agrochemicals. Its unique thiophene structure enhances its reactivity and selectivity, allowing for the efficient formation of carbon-carbon bonds, which is vital in the synthesis of complex organic molecules. Researchers and industry professionals value this compound for its high stability and compatibility with a range of functional groups, enabling the creation of diverse chemical architectures.

In addition to its application in organic synthesis, 5-Methyl-2-thiopheneboronic acid is also utilized in the development of advanced materials and sensors. Its boronic acid functionality allows for reversible binding with diols, making it useful in the design of molecular sensors and drug delivery systems. The compound's ability to form stable complexes with various substrates opens up new avenues for innovative applications in materials science and biochemistry, providing significant advantages over similar compounds in terms of reactivity and functional versatility.

Synonyms
5-Methylthiophene-2-boronic acid
CAS Number
162607-20-7
Purity
97 - 105% (Assay by titration)
Molecular Formula
C5H7BO2S
Molecular Weight
141.98
MDL Number
MFCD01318166
PubChem ID
2734374
Melting Point
150 °C (dec.)
Appearance
White to slightly yellow crystalline powd
Conditions
Store at ≤ -4 °C
General Information
Synonyms
5-Methylthiophene-2-boronic acid
CAS Number
162607-20-7
Purity
97 - 105% (Assay by titration)
Molecular Formula
C5H7BO2S
Molecular Weight
141.98
MDL Number
MFCD01318166
PubChem ID
2734374
Melting Point
150 °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

5-Methyl-2-thiopheneboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a crucial building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It is commonly employed in Suzuki-Miyaura coupling reactions, enabling the formation of carbon-carbon bonds, which is essential in creating complex organic structures.
  • Sensor Development: The unique properties of this boronic acid make it suitable for developing chemical sensors, particularly for detecting sugars and other biomolecules, enhancing applications in biomedical research.
  • Material Science: It is used in the fabrication of advanced materials, including polymers and nanomaterials, which are valuable in electronics and energy storage solutions.
  • Medicinal Chemistry: This compound plays a significant role in drug discovery, particularly in designing inhibitors for various biological targets, offering potential therapeutic benefits in treating diseases.

Citations