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CAS 1356087-42-7

:

B-[5-Methyl-6-(phenylmethoxy)-3-pyridinyl]boronic acid

Description:
B-[5-Methyl-6-(phenylmethoxy)-3-pyridinyl]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 and other nucleophiles. This compound features a pyridine ring substituted with a methyl group and a phenylmethoxy group, contributing to its unique chemical properties and potential applications in medicinal chemistry and organic synthesis. The boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in the formation of carbon-carbon bonds. Additionally, the presence of the phenylmethoxy group may enhance its lipophilicity and influence its biological activity. The compound's structure suggests potential interactions with biological targets, which could be explored for therapeutic applications. Overall, B-[5-Methyl-6-(phenylmethoxy)-3-pyridinyl]boronic acid exemplifies the versatility of boronic acids in organic chemistry and their significance in drug development and material science.
Formula:C13H14BNO3
InChI:InChI=1S/C13H14BNO3/c1-10-7-12(14(16)17)8-15-13(10)18-9-11-5-3-2-4-6-11/h2-8,16-17H,9H2,1H3
InChI key:InChIKey=XFSHWFVWTSYSGZ-UHFFFAOYSA-N
SMILES:O(CC1=CC=CC=C1)C2=C(C)C=C(B(O)O)C=N2
Synonyms:
  • B-[5-Methyl-6-(phenylmethoxy)-3-pyridinyl]boronic acid
  • (6-(Benzyloxy)-5-methylpyridin-3-yl)boronicacid
  • Boronic acid, B-[5-methyl-6-(phenylmethoxy)-3-pyridinyl]-
  • 2-Benzyloxy-3-methylpyridine-5-boronic acid
  • [6-(Benzyloxy)-5-methylpyridin-3-yl]boronic acid
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