CAS 1451392-35-0
:B-[2-(Methylthio)-3-thienyl]boronic acid
Description:
B-[2-(Methylthio)-3-thienyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a thienyl ring that has a methylthio substituent. This compound typically exhibits properties common to 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 thienyl moiety contributes to its aromatic character and may influence its reactivity and solubility in organic solvents. Additionally, the methylthio group can enhance the compound's electronic properties and steric effects, potentially affecting its interactions in chemical reactions. B-[2-(Methylthio)-3-thienyl]boronic acid may also play a role in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is a vital method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Overall, this compound is of interest in both academic research and industrial applications due to its unique structural features and reactivity.
Formula:C5H7BO2S2
InChI:InChI=1S/C5H7BO2S2/c1-9-5-4(6(7)8)2-3-10-5/h2-3,7-8H,1H3
InChI key:InChIKey=ZFHGPMWXARXDIA-UHFFFAOYSA-N
SMILES:S(C)C1=C(B(O)O)C=CS1
Synonyms:- Boronic acid, B-[2-(methylthio)-3-thienyl]-
- B-[2-(Methylthio)-3-thienyl]boronic acid
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