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Catalog Number:
40365
CAS Number:
175592-59-3
(5-Formylthiophen-3-yl)boronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
2-Formylthiophene-4-boronic acid, (5-Formyl-3-thienyl)boronic acid
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Product Information

(5-Formylthiophen-3-yl)boronic acid is a versatile compound that plays a significant role in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its unique ability to form stable complexes with diols, making it an essential reagent in the development of various pharmaceuticals and agrochemicals. Its functional group, the formyl group, enhances its reactivity, allowing for efficient coupling reactions in the synthesis of complex organic molecules. Researchers have utilized (5-Formylthiophen-3-yl)boronic acid in the preparation of biologically active compounds, including potential anti-cancer agents and other therapeutic molecules, showcasing its importance in drug discovery.

Moreover, this compound's distinctive thiophene structure contributes to its electronic properties, making it valuable in the field of materials science, particularly in the development of organic electronic devices. Its application in cross-coupling reactions, such as Suzuki-Miyaura coupling, further highlights its utility in creating intricate molecular architectures. With its broad range of applications in both research and industry, (5-Formylthiophen-3-yl)boronic acid stands out as a key building block for innovative chemical synthesis.

Synonyms
2-Formylthiophene-4-boronic acid, (5-Formyl-3-thienyl)boronic acid
CAS Number
175592-59-3
Purity
97 - 105% (Assay by titration)
Molecular Formula
C5H5BO3S
Molecular Weight
155.96
MDL Number
MFCD03002365
PubChem ID
11084115
Melting Point
113 °C (Lit.)
Appearance
White to off-white powder
Conditions
Store at RT
General Information
Synonyms
2-Formylthiophene-4-boronic acid, (5-Formyl-3-thienyl)boronic acid
CAS Number
175592-59-3
Purity
97 - 105% (Assay by titration)
Molecular Formula
C5H5BO3S
Molecular Weight
155.96
MDL Number
MFCD03002365
PubChem ID
11084115
Melting Point
113 °C (Lit.)
Appearance
White to off-white powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(5-Formylthiophen-3-yl)boronic 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.
  • Materials Science: It is used in the creation of conductive polymers and advanced materials, enhancing the properties of electronic devices and sensors.
  • Chemical Sensors: The compound is employed in the fabrication of chemical sensors, allowing for the detection of specific analytes in environmental monitoring and safety applications.
  • Medicinal Chemistry: Researchers utilize it in drug discovery processes, particularly for developing compounds with potential anti-cancer properties, due to its ability to form stable complexes with biomolecules.
  • Cross-Coupling Reactions: It plays a crucial role in cross-coupling reactions, which are essential for forming carbon-carbon bonds in organic chemistry, making it valuable for creating complex molecular architectures.

Citations