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CAS 1256354-90-1

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B-[2,4-Dichloro-5-(cyclopentyloxy)phenyl]boronic acid

Description:
B-[2,4-Dichloro-5-(cyclopentyloxy)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 two chlorine atoms and a cyclopentyloxy group, which contributes to its hydrophobic characteristics and may influence its biological activity. The presence of the boronic acid moiety allows for potential interactions with biological targets, particularly in the context of drug development. This compound is typically solid at room temperature and may exhibit moderate solubility in organic solvents. Its reactivity can be attributed to the boron atom, which can participate in various chemical reactions, including Suzuki coupling, a widely used method for forming carbon-carbon bonds. Overall, B-[2,4-Dichloro-5-(cyclopentyloxy)phenyl]boronic acid is a versatile compound with significant implications in synthetic and medicinal chemistry.
Formula:C11H13BCl2O3
InChI:InChI=1S/C11H13BCl2O3/c13-9-6-10(14)11(5-8(9)12(15)16)17-7-3-1-2-4-7/h5-7,15-16H,1-4H2
InChI key:InChIKey=RFDLUZMLHLCHJL-UHFFFAOYSA-N
SMILES:O(C1=CC(B(O)O)=C(Cl)C=C1Cl)C2CCCC2
Synonyms:
  • B-[2,4-Dichloro-5-(cyclopentyloxy)phenyl]boronic acid
  • Boronic acid, B-[2,4-dichloro-5-(cyclopentyloxy)phenyl]-
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