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CAS 1072951-68-8

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B-[3,5-Diformyl-2-(1-methylethoxy)phenyl]boronic acid

Description:
B-[3,5-Diformyl-2-(1-methylethoxy)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 materials science. The compound features a phenyl ring substituted with two formyl groups at the 3 and 5 positions, enhancing its reactivity and potential for further functionalization. The presence of the 1-methylethoxy group contributes to its solubility and stability in organic solvents. This compound may exhibit properties such as moderate acidity due to the boronic acid group, and it can participate in cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, its structural characteristics suggest potential applications in medicinal chemistry and as a building block in the synthesis of complex organic molecules. Overall, B-[3,5-Diformyl-2-(1-methylethoxy)phenyl]boronic acid is a versatile compound with significant implications in various fields of chemistry.
Formula:C11H13BO5
InChI:InChI=1S/C11H13BO5/c1-7(2)17-11-9(6-14)3-8(5-13)4-10(11)12(15)16/h3-7,15-16H,1-2H3
InChI key:InChIKey=MZTOPIAFLPHQPO-UHFFFAOYSA-N
SMILES:O(C(C)C)C1=C(B(O)O)C=C(C=O)C=C1C=O
Synonyms:
  • B-[3,5-Diformyl-2-(1-methylethoxy)phenyl]boronic acid
  • Boronic acid, B-[3,5-diformyl-2-(1-methylethoxy)phenyl]-
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