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CAS 1704063-87-5

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B-[2-(Ethoxymethyl)-4-fluorophenyl]boronic acid

Description:
B-[2-(Ethoxymethyl)-4-fluorophenyl]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 fluorinated aromatic ring, which can enhance its biological activity and influence its electronic properties. The ethoxymethyl substituent contributes to its solubility and reactivity, allowing for potential applications in drug development and material science. Boronic acids are typically stable under ambient conditions but can undergo hydrolysis in the presence of moisture, leading to the formation of boronic acid derivatives. This compound may also exhibit unique properties such as selective binding to certain biomolecules, making it a candidate for use in targeted therapies or as a chemical probe in biological research. Overall, B-[2-(Ethoxymethyl)-4-fluorophenyl]boronic acid represents a versatile structure with significant potential in various fields of chemistry and biochemistry.
Formula:C9H12BFO3
InChI:InChI=1S/C9H12BFO3/c1-2-14-6-7-5-8(11)3-4-9(7)10(12)13/h3-5,12-13H,2,6H2,1H3
InChI key:InChIKey=DLLCBBRHJIFXRS-UHFFFAOYSA-N
SMILES:C(OCC)C1=C(B(O)O)C=CC(F)=C1
Synonyms:
  • B-[2-(Ethoxymethyl)-4-fluorophenyl]boronic acid
  • Boronic acid, B-[2-(ethoxymethyl)-4-fluorophenyl]-
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