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CAS 850589-41-2

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B-[3-Chloro-4-[(propylamino)carbonyl]phenyl]boronic acid

Description:
B-[3-Chloro-4-[(propylamino)carbonyl]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 chlorinated phenyl ring, which enhances its reactivity and potential for biological activity. The propylamino carbonyl substituent contributes to its solubility and interaction with biological targets, potentially influencing its pharmacological properties. This compound may be utilized in the development of pharmaceuticals, particularly in the design of inhibitors for certain enzymes or receptors. Its boronic acid moiety is also significant in the context of drug delivery systems and materials science, where it can participate in cross-linking reactions. Overall, B-[3-Chloro-4-[(propylamino)carbonyl]phenyl]boronic acid exemplifies the versatility of boron-containing compounds in both synthetic and biological chemistry.
Formula:C10H13BClNO3
InChI:InChI=1S/C10H13BClNO3/c1-2-5-13-10(14)8-4-3-7(11(15)16)6-9(8)12/h3-4,6,15-16H,2,5H2,1H3,(H,13,14)
InChI key:InChIKey=TXXYHRWIMRLTSK-UHFFFAOYSA-N
SMILES:C(NCCC)(=O)C1=C(Cl)C=C(B(O)O)C=C1
Synonyms:
  • Boronic acid, B-[3-chloro-4-[(propylamino)carbonyl]phenyl]-
  • B-[3-Chloro-4-[(propylamino)carbonyl]phenyl]boronic acid
  • Boronic acid, [3-chloro-4-[(propylamino)carbonyl]phenyl]-
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