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CAS 850568-28-4

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B-[4-(4-Thiomorpholinylcarbonyl)phenyl]boronic acid

Description:
B-[4-(4-Thiomorpholinylcarbonyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a phenyl ring substituted with a thiomorpholinylcarbonyl group, which contributes to its unique chemical properties and potential biological activity. The thiomorpholine moiety may enhance solubility and facilitate interactions with biological targets, making it of interest in medicinal chemistry. Boronic acids are often utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the presence of the boronic acid group allows for potential applications in drug development, particularly in the design of inhibitors for various enzymes. The compound's structure suggests it may exhibit specific reactivity patterns and interactions due to the combination of the boron atom and the thiomorpholine ring, which could be explored in further research for its applications in pharmaceuticals or materials science.
Formula:C11H14BNO3S
InChI:InChI=1S/C11H14BNO3S/c14-11(13-5-7-17-8-6-13)9-1-3-10(4-2-9)12(15)16/h1-4,15-16H,5-8H2
InChI key:InChIKey=YMJVTCLBGVZIKM-UHFFFAOYSA-N
SMILES:C(=O)(C1=CC=C(B(O)O)C=C1)N2CCSCC2
Synonyms:
  • (4-(Thiomorpholine-4-carbonyl)phenyl)boronicacid
  • B-[4-(4-Thiomorpholinylcarbonyl)phenyl]boronic acid
  • Boronic acid, [4-(4-thiomorpholinylcarbonyl)phenyl]-
  • [4-(Thiomorpholin-4-ylcarbonyl)phenyl]boronic acid
  • boronic acid, B-[4-(4-thiomorpholinylcarbonyl)phenyl]-
  • [4-(Thiomorpholine-4-carbonyl)phenyl]boronic acid
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