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CAS 957062-54-3

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B-[4-(Ethoxymethoxy)phenyl]boronic acid

Description:
B-[4-(Ethoxymethoxy)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 an ethoxymethoxy group, enhancing its solubility and reactivity. Typically, boronic acids exhibit moderate stability under ambient conditions but can be sensitive to moisture and air, necessitating careful handling and storage. This compound may also participate in Suzuki-Miyaura cross-coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Its unique structure allows for potential applications in drug development, particularly in the design of inhibitors targeting specific biological pathways. Additionally, the presence of the boronic acid moiety can facilitate the formation of complexes with biomolecules, making it a valuable tool in chemical biology. Overall, B-[4-(Ethoxymethoxy)phenyl]boronic acid exemplifies the versatility of boron-containing compounds in modern chemistry.
Formula:C9H13BO4
InChI:InChI=1S/C9H13BO4/c1-2-13-7-14-9-5-3-8(4-6-9)10(11)12/h3-6,11-12H,2,7H2,1H3
InChI key:InChIKey=JKJOKHKGCAHUJY-UHFFFAOYSA-N
SMILES:O(COCC)C1=CC=C(B(O)O)C=C1
Synonyms:
  • B-[4-(Ethoxymethoxy)phenyl]boronic acid
  • Boronic acid, B-[4-(ethoxymethoxy)phenyl]-
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