CAS 950603-39-1
:5-(4-Morpholinylmethyl)thiophene-2-boronic acid pinacol ester
Description:
5-(4-Morpholinylmethyl)thiophene-2-boronic acid pinacol ester is a chemical compound characterized by its boronic acid functionality, which is crucial for applications in organic synthesis, particularly in Suzuki coupling reactions. The presence of the thiophene ring contributes to its aromatic properties, enhancing its stability and reactivity. The morpholinylmethyl group provides solubility and can facilitate interactions with biological targets, making this compound of interest in medicinal chemistry. As a pinacol ester, it exhibits a specific structural arrangement that influences its reactivity and stability, particularly in the presence of moisture or under acidic conditions. The compound is typically handled with care due to the potential reactivity of boronic acids and their derivatives. Its applications may extend to materials science and pharmaceuticals, where it can serve as a building block for more complex molecules. Overall, this compound exemplifies the intersection of organic chemistry and functional material design, showcasing the versatility of boronic acid derivatives in various chemical contexts.
Formula:C15H24BNO3S
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Found 3 products.
5-(Morpholinomethyl)thiophene-2-boronic acid, pinacol ester
CAS:Formula:C15H24BNO3SPurity:98%Color and Shape:SolidMolecular weight:309.23204-{[5-(Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophen-2-yl]methyl}morpholine
CAS:<p>4-{[5-(Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophen-2-yl]methyl}morpholine</p>Purity:98%Molecular weight:309.23195g/mol4-((5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophen-2-yl)methyl)morpholine
CAS:Formula:C15H24BNO3SPurity:95.0%Color and Shape:SolidMolecular weight:309.23


