Alkyne-Reactive
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Chromeo™ 642 azide | sc-364713 | 1 mg | $286.00 | |||
Chromeo™ 642 azide exhibits intriguing reactivity as an alkyne, characterized by its ability to participate in click chemistry through the formation of stable triazole linkages. Its azide functional group enables efficient cycloaddition reactions, showcasing rapid kinetics and high selectivity. The compound's unique electronic properties facilitate strong dipole interactions, enhancing its solubility in polar solvents. Additionally, Chromeo™ 642 azide's structural rigidity contributes to its distinct conformational stability, influencing its reactivity profile in synthetic applications. | ||||||
CruzQuench™ 5 azide | sc-362660 | 1 mg | $369.00 | |||
CruzQuench™ 5 azide exhibits exceptional reactivity as an alkyne, characterized by its ability to engage in click chemistry with remarkable efficiency. The azide moiety enhances its electrophilic nature, facilitating rapid formation of stable adducts. Its unique steric profile and electronic distribution promote selective interactions, leading to distinct reaction pathways. Additionally, the compound's solubility is influenced by its polar characteristics, allowing for versatile applications in synthetic chemistry. | ||||||
CruzQuench™ 4 azide | sc-362651 | 1 mg | $195.00 | |||
CruzQuench™ 4 azide stands out as a highly reactive alkyne, showcasing a distinctive propensity for cycloaddition reactions. Its azide group significantly enhances its nucleophilicity, enabling swift and selective interactions with various electrophiles. The compound's unique spatial arrangement and electronic properties foster diverse reaction kinetics, allowing for the formation of complex structures. Furthermore, its solubility profile is tailored for compatibility with a range of solvents, enhancing its utility in synthetic applications. | ||||||
CruzQuench™ 6 azide | sc-362669 | 1 mg | $295.00 | |||
CruzQuench™ 6 azide exhibits remarkable reactivity as an alkyne, characterized by its ability to engage in rapid click chemistry. The presence of the azide moiety facilitates efficient dipolar cycloaddition, leading to the formation of stable triazoles. Its unique steric and electronic configuration promotes selective binding with metal catalysts, enhancing reaction rates. Additionally, the compound's tunable solubility allows for versatile applications in diverse chemical environments. | ||||||