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CAS 2121513-34-4

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B-(2-Bromo-5-thiazolyl)boronic acid

Description:
B-(2-Bromo-5-thiazolyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group and a thiazole ring substituted with a bromine atom. 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 thiazole moiety contributes to its potential biological activity, as thiazoles are often found in pharmaceuticals and agrochemicals. The bromine substituent can enhance the compound's reactivity and facilitate further chemical modifications. In terms of solubility, boronic acids generally have moderate solubility in polar solvents, which can influence their reactivity and application in coupling reactions, such as Suzuki-Miyaura cross-coupling. Overall, B-(2-Bromo-5-thiazolyl)boronic acid is a versatile compound with significant utility in synthetic organic chemistry and potential therapeutic applications.
Formula:C3H3BBrNO2S
InChI:InChI=1S/C3H3BBrNO2S/c5-3-6-1-2(9-3)4(7)8/h1,7-8H
InChI key:InChIKey=VCBXYNRKOPBEGH-UHFFFAOYSA-N
SMILES:B(O)(O)C=1SC(Br)=NC1
Synonyms:
  • B-(2-Bromo-5-thiazolyl)boronic acid
  • Boronic acid, B-(2-bromo-5-thiazolyl)-
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