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Catalog Number:
40370
CAS Number:
162607-18-3
5-Chloro-2-thiopheneboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
5-Chlorothiophene-2-boronic acid
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Product Information

5-Chloro-2-thiopheneboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its unique structure, featuring a thiophene ring, enhances its reactivity and compatibility with various substrates, allowing for the development of innovative materials and compounds.

Researchers and industry professionals appreciate 5-Chloro-2-thiopheneboronic acid for its role in the creation of biologically active compounds, particularly in the development of targeted therapies and drug discovery. Its stability and ease of handling further contribute to its appeal in laboratory settings. With applications spanning from synthetic organic chemistry to material science, this compound stands out as a valuable tool for advancing research and development in various fields.

Synonyms
5-Chlorothiophene-2-boronic acid
CAS Number
162607-18-3
Purity
97 - 105% (Assay by titration)
Molecular Formula
C4H4BClO2S
Molecular Weight
162.39
MDL Number
MFCD00236030
PubChem ID
2734324
Melting Point
140 °C (Lit.)
Appearance
White to slightly yellow crystalline powd
Conditions
Store at RT
General Information
Synonyms
5-Chlorothiophene-2-boronic acid
CAS Number
162607-18-3
Purity
97 - 105% (Assay by titration)
Molecular Formula
C4H4BClO2S
Molecular Weight
162.39
MDL Number
MFCD00236030
PubChem ID
2734324
Melting Point
140 °C (Lit.)
Appearance
White to slightly yellow crystalline powd
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-Chloro-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.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds in complex organic compounds, making it valuable in material science and drug discovery.
  • Fluorescent Probes: The unique properties of this boronic acid allow it to be used in designing fluorescent probes for biological imaging, aiding researchers in studying cellular processes.
  • Sensor Development: It plays a role in the development of chemical sensors for detecting sugars and other biomolecules, which is crucial in fields like diagnostics and environmental monitoring.
  • Material Science: The compound is utilized in the production of conductive polymers and materials, enhancing the performance of electronic devices and sensors.

Citations