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CAS 2096332-07-7

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3-Chloro-5-(dihydroxyboranyl)thiophene-2-boronic acid

Description:
3-Chloro-5-(dihydroxyboranyl)thiophene-2-boronic acid is a boronic acid derivative featuring a thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. This compound is characterized by the presence of a chlorine atom and a boron moiety with two hydroxyl groups, contributing to its unique reactivity and potential applications in organic synthesis and medicinal chemistry. The boronic acid functional group is known for its ability to form reversible covalent bonds with diols, making it useful in various chemical reactions, including Suzuki coupling. The presence of the thiophene ring may impart electronic properties that enhance its reactivity and solubility in organic solvents. Additionally, the compound's structure suggests potential applications in materials science, particularly in the development of organic semiconductors or sensors. Its specific properties, such as solubility, stability, and reactivity, would depend on the surrounding conditions, including pH and solvent environment. Overall, this compound represents a versatile building block in synthetic organic chemistry.
Formula:C4H5B2ClO4S
InChI:InChI=1S/C4H5B2ClO4S/c7-2-1-3(5(8)9)12-4(2)6(10)11/h1,8-11H
InChI key:InChIKey=HWPJMSMTYFBAGQ-UHFFFAOYSA-N
SMILES:B(O)(O)C=1SC(B(O)O)=C(Cl)C1
Synonyms:
  • 3-Chlorothiophene-2,5-diboronic acid
  • 3-Chloro-5-(dihydroxyboranyl)thiophene-2-boronic acid
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