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CAS 1309980-90-2

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B-[6-Bromo-2-chloro-3-(phenylmethoxy)phenyl]boronic acid

Description:
B-[6-Bromo-2-chloro-3-(phenylmethoxy)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 phenylmethoxy group, which enhances its solubility and reactivity, and halogen substituents (bromo and chloro) that can influence its electronic properties and reactivity. The presence of these substituents can also affect its interactions in biological systems, potentially making it a candidate for drug development or as a tool in chemical biology. Additionally, boronic acids are often utilized in Suzuki coupling reactions, which are pivotal in forming carbon-carbon bonds in the synthesis of complex organic molecules. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and their potential applications in various fields, including pharmaceuticals and materials science.
Formula:C13H11BBrClO3
InChI:InChI=1S/C13H11BBrClO3/c15-10-6-7-11(13(16)12(10)14(17)18)19-8-9-4-2-1-3-5-9/h1-7,17-18H,8H2
InChI key:InChIKey=VXBLINFXGJRKAF-UHFFFAOYSA-N
SMILES:O(CC1=CC=CC=C1)C2=C(Cl)C(B(O)O)=C(Br)C=C2
Synonyms:
  • Boronic acid, B-[6-bromo-2-chloro-3-(phenylmethoxy)phenyl]-
  • B-[6-Bromo-2-chloro-3-(phenylmethoxy)phenyl]boronic acid
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