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CAS 2121513-98-0

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B-[3-Bromo-2-(methylthio)phenyl]boronic acid

Description:
B-[3-Bromo-2-(methylthio)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a bromine atom and a methylthio group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The bromine substituent can enhance the reactivity of the phenyl ring, facilitating electrophilic aromatic substitution reactions. The methylthio group may influence the electronic properties of the molecule, potentially affecting its reactivity and solubility. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are vital in the formation of carbon-carbon bonds in organic synthesis. Overall, B-[3-Bromo-2-(methylthio)phenyl]boronic acid is a versatile compound with significant implications in chemical research and development.
Formula:C7H8BBrO2S
InChI:InChI=1S/C7H8BBrO2S/c1-12-7-5(8(10)11)3-2-4-6(7)9/h2-4,10-11H,1H3
InChI key:InChIKey=VDQNQEDCECCQMB-UHFFFAOYSA-N
SMILES:S(C)C1=C(B(O)O)C=CC=C1Br
Synonyms:
  • Boronic acid, B-[3-bromo-2-(methylthio)phenyl]-
  • B-[3-Bromo-2-(methylthio)phenyl]boronic acid
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