Thiophenes
Items 381 to 384 of 384 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Rivaroxaban-d4 | 1132681-38-9 | sc-219982 | 1 mg | $388.00 | 3 | |
Rivaroxaban-d4, a thiophene derivative, showcases unique electronic characteristics attributed to its thiophene framework, which facilitates strong charge transfer interactions. The presence of deuterated groups enhances its stability and alters reaction kinetics, providing insights into isotopic effects on molecular behavior. Its planar geometry promotes effective π-π interactions, while the functional groups contribute to selective reactivity, allowing for diverse synthetic pathways and transformations. | ||||||
3-ethyl-5-(4-fluorophenyl)-2-mercaptothieno[2,3-d]pyrimidin-4(3H)-one | sc-346902 sc-346902A | 250 mg 1 g | $197.00 $399.00 | |||
3-ethyl-5-(4-fluorophenyl)-2-mercaptothieno[2,3-d]pyrimidin-4(3H)-one exhibits intriguing properties due to its thieno-pyrimidine structure, which enables unique hydrogen bonding and dipole-dipole interactions. The fluorophenyl substituent enhances electron-withdrawing effects, influencing reactivity and stability. Its thiol group introduces nucleophilic characteristics, facilitating diverse reaction mechanisms, while the compound's rigid conformation supports effective stacking interactions, impacting solubility and aggregation behavior. | ||||||
3-methyl-2-[(thien-2-ylcarbonyl)amino]butanoic acid | sc-347122 sc-347122A | 1 g 5 g | $208.00 $625.00 | |||
3-methyl-2-[(thien-2-ylcarbonyl)amino]butanoic acid showcases distinctive characteristics attributed to its thiophene moiety, which enhances π-π stacking and facilitates electron delocalization. The thienylcarbonyl group introduces a polar functional site, promoting strong intermolecular interactions and influencing solubility profiles. Its unique structural arrangement allows for selective reactivity in condensation reactions, while the acid's carboxylic group contributes to its acidity and potential for forming stable salts. | ||||||
2-oxo-3-thien-2-ylpropanoic acid | 15504-41-3 | sc-343150 sc-343150A | 250 mg 1 g | $240.00 $487.00 | ||
2-oxo-3-thien-2-ylpropanoic acid exhibits intriguing properties due to its thiophene structure, which enhances its ability to engage in hydrogen bonding and facilitates unique charge transfer interactions. The presence of the carbonyl group increases electrophilicity, making it a reactive participant in various condensation and addition reactions. Its distinct spatial configuration allows for selective interactions with nucleophiles, influencing reaction kinetics and pathways in synthetic applications. | ||||||