Intermediates
Items 241 to 250 of 255 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
AGN 193109 Ethyl Ester | 171568-43-7 | sc-207265 | 1 mg | $393.00 | ||
AGN 193109 Ethyl Ester functions as a notable intermediate, distinguished by its reactivity as an acid halide. Its structure allows for efficient acylation reactions, where it can readily interact with nucleophiles, leading to the formation of esters and amides. The presence of the ethyl group enhances solubility and facilitates smoother reaction kinetics. Additionally, its ability to stabilize transition states contributes to its effectiveness in various synthetic pathways, promoting diverse chemical transformations. | ||||||
rac 8-Hydroxy Efavirenz | 205754-32-1 | sc-208270 sc-208270A sc-208270B | 1 mg 2 mg 5 mg | $357.00 $637.00 $1380.00 | ||
Rac 8-Hydroxy Efavirenz serves as a versatile intermediate, characterized by its unique ability to engage in selective electrophilic reactions. Its hydroxyl group enhances hydrogen bonding interactions, influencing solubility and reactivity profiles. This compound exhibits distinct pathways for nucleophilic attack, allowing for the formation of complex molecular architectures. The steric and electronic properties of its structure facilitate rapid reaction kinetics, making it a valuable component in synthetic chemistry. | ||||||
Desbutyl Lumefantrine | 252990-19-5 | sc-391626 | 1 mg | $380.00 | ||
Desbutyl Lumefantrine functions as a notable intermediate, distinguished by its capacity for diverse coupling reactions. Its structural features promote unique π-π stacking interactions, enhancing stability in various environments. The compound's reactivity is influenced by its electron-rich regions, allowing for efficient participation in cross-coupling processes. Additionally, its conformational flexibility contributes to varied reaction pathways, optimizing synthetic routes in complex organic synthesis. | ||||||
BAY 41-2272 | 256376-24-6 | sc-202491 sc-202491A | 5 mg 25 mg | $233.00 $714.00 | 4 | |
BAY 41-2272 serves as a versatile intermediate, characterized by its ability to engage in selective nucleophilic substitutions. The compound exhibits strong hydrogen bonding capabilities, which facilitate unique interactions with various substrates. Its distinct electronic configuration allows for rapid reaction kinetics, making it a key player in multi-step synthesis. Furthermore, its solubility properties enhance its compatibility with diverse reaction media, promoting efficient transformations in organic chemistry. | ||||||
SMER28 | 307538-42-7 | sc-222320 | 10 mg | $173.00 | ||
SMER28 functions as a notable intermediate, distinguished by its reactivity as an acid halide. It readily participates in acylation reactions, showcasing a propensity for electrophilic attack on nucleophiles. The compound's unique steric and electronic properties influence its reaction pathways, leading to diverse product formation. Additionally, its ability to stabilize transition states enhances reaction rates, making it a crucial component in complex synthetic routes. | ||||||
WAY 267464 dihydrochloride | 1432043-31-6 | sc-361405 | 10 mg | $359.00 | 1 | |
WAY 267464 dihydrochloride serves as a versatile intermediate, characterized by its strong electrophilic nature as an acid halide. It exhibits a high reactivity towards nucleophiles, facilitating rapid acylation processes. The compound's distinct electronic configuration and steric factors contribute to selective reaction pathways, allowing for the formation of varied derivatives. Its capacity to engage in multiple reaction mechanisms underscores its significance in synthetic chemistry. | ||||||
4-Defluoro-4-hydroxy Gefitinib | 847949-50-2 | sc-391838 | 25 mg | $465.00 | ||
4-Defluoro-4-hydroxy Gefitinib functions as a notable intermediate, distinguished by its unique ability to stabilize reactive intermediates through intramolecular hydrogen bonding. This compound exhibits selective reactivity due to its electron-withdrawing fluorine substituents, which influence nucleophilic attack patterns. Its distinct steric hindrance allows for controlled reaction kinetics, enabling the formation of diverse chemical entities while minimizing side reactions. | ||||||
Inotilone | 906366-79-8 | sc-207758 | 5 mg | $164.00 | ||
Inotilone serves as a significant intermediate characterized by its capacity to engage in unique π-π stacking interactions, enhancing its stability in various reaction environments. The presence of specific functional groups facilitates selective electrophilic substitutions, allowing for tailored synthesis pathways. Its moderate polarity influences solubility and reactivity, promoting efficient coupling reactions while minimizing unwanted byproducts, thus streamlining synthetic processes. | ||||||
(2α)-Methyl Megestrol Acetate | 907193-65-1 | sc-394427 sc-394427A | 1 mg 10 mg | $390.00 $2800.00 | ||
(2α)-Methyl Megestrol Acetate acts as a versatile intermediate, notable for its ability to form hydrogen bonds that influence its reactivity in synthetic pathways. The compound exhibits a unique steric configuration, which can direct regioselectivity in reactions, enhancing the formation of desired products. Its lipophilic nature aids in solvation dynamics, promoting efficient interactions with various reagents while minimizing side reactions, thus optimizing overall yield in complex syntheses. | ||||||
Thiamet G | 1009816-48-1 | sc-224307 sc-224307A | 1 mg 5 mg | $51.00 $94.00 | 1 | |
Thiamet G serves as a pivotal intermediate, characterized by its unique ability to engage in nucleophilic substitution reactions due to its electrophilic nature. The compound's structural features facilitate specific molecular interactions, allowing for selective reactivity in diverse synthetic routes. Its stability under varying conditions enhances reaction kinetics, while its polar characteristics promote solubility in various solvents, streamlining the integration into multi-step synthesis processes. | ||||||