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Catalog Number:
40394
CAS Number:
4347-33-5
5-Formyl-2-thiopheneboronic acid
Purity:
≥ 96% (HPLC)
Synonym(s):
5-Formyl-2-thienylboronic acid
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Product Information

5-Formyl-2-thiopheneboronic acid is a versatile compound recognized for its unique properties and applications in organic synthesis and medicinal chemistry. This boronic acid derivative features a thiophene ring, which enhances its reactivity and makes it an excellent building block for the development of various organic molecules. Its ability to form stable complexes with diols and other Lewis bases allows it to play a crucial role in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds essential for creating complex organic structures.

Researchers and industry professionals can leverage 5-Formyl-2-thiopheneboronic acid in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its application in the preparation of biologically active compounds, such as anti-cancer agents and other therapeutic drugs, highlights its significance in drug discovery and development. Moreover, its compatibility with various reaction conditions makes it a preferred choice for chemists seeking efficient and reliable reagents in their synthetic pathways.

Synonyms
5-Formyl-2-thienylboronic acid
CAS Number
4347-33-5
Purity
≥ 96% (HPLC)
Molecular Formula
C5H5BO3S
Molecular Weight
155.96
MDL Number
MFCD02093666
PubChem ID
2773430
Melting Point
132 - 135 °C
Appearance
Light brown solid
Conditions
Store at 2 - 8 °C
General Information
Synonyms
5-Formyl-2-thienylboronic acid
CAS Number
4347-33-5
Purity
≥ 96% (HPLC)
Molecular Formula
C5H5BO3S
Molecular Weight
155.96
MDL Number
MFCD02093666
PubChem ID
2773430
Melting Point
132 - 135 °C
Appearance
Light brown solid
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-Formyl-2-thiopheneboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Drug Development: Its unique boronic acid functionality allows for the creation of biologically active compounds, making it valuable in medicinal chemistry for designing new drugs.
  • Material Science: Used in the production of conductive polymers and organic electronics, it enhances the performance of materials in devices like solar cells and sensors.
  • Catalysis: This compound acts as a catalyst in various chemical reactions, improving efficiency and selectivity in processes such as cross-coupling reactions.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential in diagnostics and therapeutic applications.

Citations