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Catalog Number:
40385
CAS Number:
17303-83-2
Ácido 3-formil-2-tiofenoborónico
Purity:
95 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 3-formil-2-tienilborónico
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$94.54 /1G
Tamaño
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Product Information

3-Formyl-2-thiopheneboronic acid is a versatile compound recognized for its unique boronic acid functionality, which makes it an essential building block in organic synthesis and medicinal chemistry. This compound features a thiophene ring, enhancing its electronic properties and making it particularly valuable in the development of pharmaceuticals and agrochemicals. Its ability to form stable complexes with various substrates allows for its application in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is widely utilized in the synthesis of complex organic molecules.

Researchers and industry professionals can leverage 3-Formyl-2-thiopheneboronic acid in the design of novel materials and drug candidates, particularly in the fields of organic electronics and cancer therapeutics. Its distinctive structure not only contributes to improved reactivity but also offers potential advantages over similar compounds, such as enhanced solubility and selectivity in reactions. This compound is an excellent choice for those looking to innovate in synthetic methodologies or explore new avenues in material science.

Synonyms
Ácido 3-formil-2-tienilborónico
CAS Number
17303-83-2
Purity
95 - 105% (Ensayo por titulación)
Molecular Formula
C5H5BO3S
Molecular Weight
155.96
MDL Number
MFCD01075679
PubChem ID
2773429
Melting Point
330 °C (descenso)
Appearance
Polvo de color blanco a naranja claro a verde.
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
Ácido 3-formil-2-tienilborónico
CAS Number
17303-83-2
Purity
95 - 105% (Ensayo por titulación)
Molecular Formula
C5H5BO3S
Molecular Weight
155.96
MDL Number
MFCD01075679
PubChem ID
2773429
Melting Point
330 °C (descenso)
Appearance
Polvo de color blanco a naranja claro a verde.
Conditions
Conservar entre 2 y 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-Formyl-2-thiopheneboronic 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.
  • Medicinal Chemistry: It plays a crucial role in the design of novel therapeutic agents, especially in targeting specific biological pathways due to its unique boronic acid functionality.
  • Material Science: The compound is used in the fabrication of advanced materials, including conductive polymers and organic semiconductors, enhancing the performance of electronic devices.
  • Chemical Sensors: Its properties make it suitable for developing sensors that detect specific biomolecules, which is valuable in medical diagnostics and environmental monitoring.
  • Cross-Coupling Reactions: It is effective in palladium-catalyzed cross-coupling reactions, facilitating the formation of carbon-carbon bonds, which is essential in creating complex molecular architectures.

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