Acetylation
Items 41 to 50 of 80 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
AN-9 | 122110-53-6 | sc-364403 sc-364403A | 5 mg 25 mg | $72.00 $269.00 | ||
AN-9 exhibits remarkable properties as an acetylation agent, primarily due to its electrophilic nature as an acid halide. The compound engages in swift acyl transfer reactions, driven by its strong electrophilicity, which promotes effective nucleophilic attack by alcohols and amines. Its unique steric and electronic characteristics enable selective acetylation, while its compatibility with diverse reaction environments allows for tailored synthetic pathways, enhancing its utility in organic chemistry. | ||||||
PTACH | 848354-66-5 | sc-253326 | 2 mg | $216.00 | ||
PTACH serves as a potent acetylation agent, characterized by its reactivity as an acid halide. Its electrophilic carbonyl carbon facilitates rapid acylation, allowing for efficient interactions with nucleophiles such as alcohols and amines. The compound's unique steric hindrance and electronic properties enable regioselective acetylation, while its stability under various conditions supports diverse synthetic strategies, making it a versatile tool in organic synthesis. | ||||||
L-Lysine | 56-87-1 | sc-207804 sc-207804A sc-207804B | 25 g 100 g 1 kg | $93.00 $258.00 $519.00 | ||
L-Lysine, when acting as an acetylation agent, showcases its ability to form stable acetamide derivatives through nucleophilic attack on electrophilic carbon centers. The amino group enhances its reactivity, promoting selective acylation pathways. Its unique side chain contributes to steric effects that influence reaction kinetics, allowing for tailored modifications in complex organic frameworks. This behavior underscores its role in facilitating diverse chemical transformations. | ||||||
Droxinostat | 99873-43-5 | sc-364485 sc-364485A | 5 mg 25 mg | $85.00 $454.00 | 1 | |
Droxinostat, as an acetylation agent, exhibits a distinctive reactivity profile due to its structural features that facilitate electrophilic interactions. The presence of specific functional groups allows for efficient nucleophilic attacks, leading to the formation of stable acetyl derivatives. Its unique steric and electronic properties influence the selectivity of acylation reactions, enabling precise modifications in various chemical environments. This behavior highlights its potential in advancing synthetic methodologies. | ||||||
BML-210 | 537034-17-6 | sc-221369 sc-221369A | 1 mg 5 mg | $90.00 $272.00 | ||
BML-210, functioning as an acetylation agent, showcases remarkable reactivity attributed to its unique electronic configuration and steric hindrance. The compound's ability to stabilize transition states enhances its acylation efficiency, promoting rapid nucleophilic attacks. Its distinctive molecular interactions facilitate selective acetylation, allowing for tailored modifications in diverse substrates. This specificity underscores its role in refining synthetic pathways and optimizing reaction conditions. | ||||||
Biphenyl-4-sulfonyl chloride | 1623-93-4 | sc-254973 | 5 g | $55.00 | ||
Biphenyl-4-sulfonyl chloride, as an acetylation agent, exhibits exceptional electrophilic character due to its strong electron-withdrawing sulfonyl group. This enhances its reactivity towards nucleophiles, leading to efficient acyl transfer. The compound's rigid biphenyl structure contributes to its stability and selectivity in reactions, allowing for precise control over acylation processes. Its unique interaction dynamics facilitate the formation of stable intermediates, streamlining synthetic routes. | ||||||
SIRT1/2 Inhibitor VII | 143034-06-4 | sc-364618 | 10 mg | $113.00 | ||
SIRT1/2 Inhibitor VII, functioning as an acetylation agent, showcases remarkable specificity in targeting acetylation sites due to its unique structural motifs. The compound's ability to form transient complexes with acetyl groups enhances its reactivity, promoting selective modifications of target proteins. Its distinct steric and electronic properties facilitate rapid reaction kinetics, allowing for efficient acyl transfer while minimizing side reactions, thus optimizing synthetic pathways. | ||||||
AK-7 | 420831-40-9 | sc-364096 sc-364096A sc-364096B | 5 mg 25 mg 100 mg | $54.00 $221.00 $880.00 | ||
AK-7, as an acetylation agent, exhibits a unique reactivity profile characterized by its ability to engage in electrophilic interactions with nucleophilic sites on substrates. The compound's distinctive steric hindrance and electronic distribution enable it to preferentially form stable intermediates, enhancing the efficiency of acyl transfer reactions. This specificity not only accelerates reaction kinetics but also reduces byproduct formation, streamlining synthetic processes in complex chemical environments. | ||||||
(S)-HDAC-42 | 935881-37-1 | sc-296364 sc-296364A | 1 mg 5 mg | $94.00 $409.00 | ||
(S)-HDAC-42 functions as an acetylation agent, showcasing remarkable selectivity in targeting specific amino acid residues. Its unique chiral structure facilitates precise molecular recognition, allowing for tailored interactions with histone proteins. The compound's ability to modulate reaction pathways through dynamic conformational changes enhances its reactivity, promoting efficient acylation while minimizing side reactions. This behavior underscores its potential in fine-tuning biochemical processes. | ||||||
Pimelic Diphenylamide 106 | 937039-45-7 | sc-364589 sc-364589A | 1 mg 5 mg | $41.00 $74.00 | ||
Pimelic Diphenylamide 106 acts as an effective acetylation agent, characterized by its ability to form stable acyl-enzyme intermediates. Its unique electronic properties facilitate strong interactions with nucleophilic sites, enhancing reaction rates. The compound exhibits a distinct preference for certain substrates, driven by steric and electronic factors that influence selectivity. Additionally, its robust stability under various conditions allows for controlled reaction environments, optimizing acylation efficiency. | ||||||