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CAS 849052-25-1

:

B-[4-[(4-Chloro-3-methylphenoxy)methyl]phenyl]boronic acid

Description:
B-[4-[(4-Chloro-3-methylphenoxy)methyl]phenyl]boronic acid, identified by its CAS number 849052-25-1, is an organoboron compound characterized by the presence of a boronic acid functional group. This compound features a phenyl ring substituted with a chloromethyl group and a phenoxy moiety, which contributes to its potential applications in medicinal chemistry and materials science. The boronic acid group is known for its ability to form reversible covalent bonds with diols, making it useful in various chemical reactions, including Suzuki coupling reactions, which are pivotal in organic synthesis. Additionally, the presence of the chloro and methyl substituents on the aromatic rings can influence the compound's reactivity, solubility, and biological activity. Typically, boronic acids exhibit moderate to high solubility in polar organic solvents, and their properties can be further modified through structural variations. Overall, this compound's unique structure and functional groups make it a valuable candidate for research in drug development and synthetic chemistry.
Formula:C14H14BClO3
InChI:InChI=1/C14H14BClO3/c1-10-8-13(6-7-14(10)16)19-9-11-2-4-12(5-3-11)15(17)18/h2-8,17-18H,9H2,1H3
InChI key:InChIKey=OUKUADBAEFEIGP-UHFFFAOYSA-N
SMILES:C(OC1=CC(C)=C(Cl)C=C1)C2=CC=C(B(O)O)C=C2
Synonyms:
  • (4-((4-Chloro-3-methylphenoxy)methyl)phenyl)boronic acid
  • [4-(4-Chloro-3-methylphenoxymethyl)phenyl]boronic acid
  • Boronic acid, [4-[(4-chloro-3-methylphenoxy)methyl]phenyl]-
  • Boronic acid, B-[4-[(4-chloro-3-methylphenoxy)methyl]phenyl]-
  • B-[4-[(4-Chloro-3-methylphenoxy)methyl]phenyl]boronic acid
  • See more synonyms
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