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Catalog Number:
40381
CAS Number:
162607-15-0
4-Methyl-2-thiopheneboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
4-methylthiophene-2-boronic acid
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Product Information

4-Methyl-2-thiopheneboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its unique ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the synthesis of various biaryl compounds. Its distinctive thiophene ring enhances its electronic properties, allowing for improved reactivity and selectivity in coupling reactions. Researchers and industry professionals can leverage this compound in the development of pharmaceuticals, agrochemicals, and advanced materials, where precise molecular structures are crucial.

In addition to its synthetic applications, 4-Methyl-2-thiopheneboronic acid has shown promise in the field of sensor technology, particularly in the detection of biomolecules. Its functional properties enable the design of sensitive and selective sensors, which can be pivotal in medical diagnostics and environmental monitoring. The compound's stability and ease of handling further enhance its appeal, making it a valuable asset in both laboratory and industrial settings.

Synonyms
4-methylthiophene-2-boronic acid
CAS Number
162607-15-0
Purity
97 - 105% (Assay by titration)
Molecular Formula
C5H7BO2S
Molecular Weight
141.98
MDL Number
MFCD01319040
PubChem ID
2734373
Melting Point
125 - 126 °C
Density
1.30 g/mL
Appearance
White to slightly yellow crystalline powd
Refractive Index
n20D 1.55
Conditions
Store at 2 - 8 °C
General Information
Synonyms
4-methylthiophene-2-boronic acid
CAS Number
162607-15-0
Purity
97 - 105% (Assay by titration)
Molecular Formula
C5H7BO2S
Molecular Weight
141.98
MDL Number
MFCD01319040
PubChem ID
2734373
Melting Point
125 - 126 °C
Density
1.30 g/mL
Appearance
White to slightly yellow crystalline powd
Refractive Index
n20D 1.55
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

4-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 used in Suzuki-Miyaura coupling reactions, allowing researchers to create complex carbon-carbon bonds, which are essential in the formation of advanced materials.
  • Sensor Development: The unique properties of this boronic acid make it ideal for developing sensors that detect sugars and other biomolecules, benefiting the food and healthcare industries.
  • Material Science: It is employed in the creation of conductive polymers and materials, enhancing the performance of electronic devices and renewable energy technologies.
  • Medicinal Chemistry: Researchers utilize it in drug discovery processes, particularly for targeting specific biological pathways, leading to more effective treatments with fewer side effects.

Citations