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CAS 1217501-04-6

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B-[4-[(Cyclopropylmethyl)sulfinyl]phenyl]boronic acid

Description:
B-[4-[(Cyclopropylmethyl)sulfinyl]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, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a cyclopropylmethyl sulfinyl group, which contributes to its unique reactivity and potential biological activity. The sulfinyl moiety can enhance the compound's solubility and stability, while the boronic acid group can participate in cross-coupling reactions, a key process in the formation of carbon-carbon bonds. This compound may exhibit interesting properties such as selective reactivity and potential therapeutic effects, particularly in the context of drug development. Its structural characteristics suggest it could be explored for applications in areas such as cancer therapy or as a tool in chemical biology. As with many boronic acids, it is important to handle this compound with care due to its reactivity and potential environmental impact.
Formula:C10H13BO3S
InChI:InChI=1S/C10H13BO3S/c12-11(13)9-3-5-10(6-4-9)15(14)7-8-1-2-8/h3-6,8,12-13H,1-2,7H2
InChI key:InChIKey=LVSXKKKBVXTPSI-UHFFFAOYSA-N
SMILES:S(CC1CC1)(=O)C2=CC=C(B(O)O)C=C2
Synonyms:
  • B-[4-[(Cyclopropylmethyl)sulfinyl]phenyl]boronic acid
  • Boronic acid, B-[4-[(cyclopropylmethyl)sulfinyl]phenyl]-
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