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CAS 177735-11-4

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(4-Methylthien-3-yl)boronic acid

Description:
(4-Methylthien-3-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a thienyl ring. This compound features a thiophene ring substituted with a methyl group at the 4-position and a boronic acid group at the 3-position. It is typically a white to off-white solid and is soluble in polar organic solvents. The boronic acid functionality allows for the formation of reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and as a reagent in Suzuki coupling reactions. Additionally, this compound may exhibit properties relevant to medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. Its reactivity and ability to form complexes with other molecules make it a valuable building block in the synthesis of more complex organic structures. As with many boronic acids, it is important to handle this compound with care, as it may be sensitive to moisture and air.
Formula:C5H7BO2S
InChI:InChI=1S/C5H7BO2S/c1-4-2-9-3-5(4)6(7)8/h2-3,7-8H,1H3
InChI key:InChIKey=LVPFZXKLROORIK-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C(C)=CSC1
Synonyms:
  • (4-Methylthien-3-yl)boronic acid
  • (4-Methylthiophen-3-Yl)Boronic Acid
  • (4-Methylthiophen-3-yl)dihydroxyborane
  • 4-Methylthiophene-3-boronic acid
  • B-(4-Methyl-3-thienyl)boronic acid
  • Boronic acid, (4-methyl-3-thienyl)-
  • Boronic acid, B-(4-methyl-3-thienyl)-
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