CAS 321438-86-2
:6-(Methylthio)pyridine-3-boronic acid
Description:
6-(Methylthio)pyridine-3-boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine 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 methylthio group enhances its solubility in organic solvents and may influence its reactivity and interaction with biological targets. Additionally, the pyridine ring contributes to its aromatic character and potential for coordination with metal ions. The compound is often utilized in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its unique structure allows for specific interactions in biological systems, making it a candidate for further research in drug development and material science. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity and reactivity.
Formula:C6H8BNO2S
InChI:InChI=1/C6H8BNO2S/c1-11-6-3-2-5(4-8-6)7(9)10/h2-4,9-10H,1H3
SMILES:CSc1ccc(cn1)B(O)O
Synonyms:- [6-(Methylsulfanyl)pyridin-3-yl]boronic acid
- 2-(Methylthio)-pyridine-5-boronic acid
- Boronic acid, B-[6-(methylthio)-3-pyridinyl]-
- 6-(Methylthio)pyridin-3-ylboronicacid
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Found 3 products.
2-(METHYLTHIO)-5-PYRIDINYL-BORONIC ACID
CAS:Formula:C6H8BNO2SPurity:95%Color and Shape:SolidMolecular weight:169.00926-(Methylsulphanyl)pyridine-3-boronic acid
CAS:<p>6-(Methylsulphanyl)pyridine-3-boronic acid</p>Formula:C6H8BNO2SPurity:98%Color and Shape: off white solidMolecular weight:169.00922g/mol6-(Methylthio)pyridin-3-ylboronic acid
CAS:Formula:C6H8BNO2SPurity:95%Color and Shape:SolidMolecular weight:169.01


