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CAS 1150114-46-7

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B-[3,5-Dichloro-4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]phenyl]boronic acid

Description:
B-[3,5-Dichloro-4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its reactivity in forming covalent bonds with diols and other nucleophiles. The compound features a phenyl ring substituted with two chlorine atoms at the 3 and 5 positions, enhancing its electronic properties and potentially influencing its reactivity. The presence of a tert-butyl dimethylsilyl ether group provides steric hindrance and may affect solubility and stability. This compound is typically used in organic synthesis, particularly in Suzuki coupling reactions, which are valuable for forming carbon-carbon bonds. Its boronic acid functionality allows it to participate in various chemical transformations, making it a useful intermediate in the synthesis of complex organic molecules. Additionally, the chlorinated phenyl group may impart unique properties that can be exploited in medicinal chemistry or materials science. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry.
Formula:C12H19BCl2O3Si
InChI:InChI=1S/C12H19BCl2O3Si/c1-12(2,3)19(4,5)18-11-9(14)6-8(13(16)17)7-10(11)15/h6-7,16-17H,1-5H3
InChI key:InChIKey=WNDFXSADTRWDGK-UHFFFAOYSA-N
SMILES:O([Si](C(C)(C)C)(C)C)C1=C(Cl)C=C(B(O)O)C=C1Cl
Synonyms:
  • B-[3,5-Dichloro-4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]phenyl]boronic acid
  • Boronic acid, B-[3,5-dichloro-4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]phenyl]-
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