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CAS 1256346-23-2

:

B-(4-Chloro-2-fluoro-3-propoxyphenyl)boronic acid

Description:
B-(4-Chloro-2-fluoro-3-propoxyphenyl)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 chemical reactions, particularly in Suzuki coupling reactions. The compound features a phenyl ring substituted with a chlorine atom and a fluorine atom, as well as a propoxy group, which contributes to its hydrophobic characteristics. The presence of these substituents can influence the compound's reactivity, solubility, and overall chemical behavior. Boronic acids are often utilized in organic synthesis, medicinal chemistry, and materials science due to their versatility. Additionally, the specific arrangement of substituents in B-(4-Chloro-2-fluoro-3-propoxyphenyl)boronic acid may impart unique electronic properties, making it a candidate for applications in drug development and as a building block in the synthesis of complex organic molecules. Its CAS number, 1256346-23-2, allows for precise identification in chemical databases and literature.
Formula:C9H11BClFO3
InChI:InChI=1S/C9H11BClFO3/c1-2-5-15-9-7(11)4-3-6(8(9)12)10(13)14/h3-4,13-14H,2,5H2,1H3
InChI key:InChIKey=RURLWBLBYLHJSQ-UHFFFAOYSA-N
SMILES:O(CCC)C1=C(F)C(B(O)O)=CC=C1Cl
Synonyms:
  • B-(4-Chloro-2-fluoro-3-propoxyphenyl)boronic acid
  • Boronic acid, B-(4-chloro-2-fluoro-3-propoxyphenyl)-
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