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CAS 2096331-77-8

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B-[3-Chloro-4-fluoro-5-(1-methylethoxy)phenyl]boronic acid

Description:
B-[3-Chloro-4-fluoro-5-(1-methylethoxy)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 chlorine atom, a fluorine atom, and an ethoxy group, which contribute to its unique reactivity and solubility properties. The presence of the boronic acid moiety allows for participation in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in the formation of carbon-carbon bonds. Additionally, the specific substitutions on the phenyl ring can influence the compound's electronic properties and steric hindrance, affecting its reactivity and interaction with biological targets. Overall, this compound is of interest in the development of pharmaceuticals and agrochemicals due to its versatile reactivity and potential applications in drug discovery and material science.
Formula:C9H11BClFO3
InChI:InChI=1S/C9H11BClFO3/c1-5(2)15-8-4-6(10(13)14)3-7(11)9(8)12/h3-5,13-14H,1-2H3
InChI key:InChIKey=OLVVISTZKBAJPC-UHFFFAOYSA-N
SMILES:O(C(C)C)C1=CC(B(O)O)=CC(Cl)=C1F
Synonyms:
  • Boronic acid, B-[3-chloro-4-fluoro-5-(1-methylethoxy)phenyl]-
  • B-[3-Chloro-4-fluoro-5-(1-methylethoxy)phenyl]boronic acid
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