Items 31 to 40 of 98 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Ranitidine | 66357-35-5 | sc-203679 | 1 g | $189.00 | ||
Ranitidine, as a furan derivative, exhibits intriguing properties due to its unique electronic structure, which allows for selective interactions with electrophiles. The furan ring's aromaticity contributes to its stability while enabling participation in electrophilic aromatic substitution reactions. Its ability to form hydrogen bonds enhances solubility in polar solvents, influencing reaction kinetics. Furthermore, the compound's steric configuration can affect its reactivity, leading to diverse synthetic pathways. | ||||||
Darunavir | 206361-99-1 | sc-218079 | 5 mg | $311.00 | 4 | |
Darunavir, classified as a furan, showcases distinctive reactivity patterns attributed to its electron-rich furan ring, which facilitates nucleophilic attack in various chemical transformations. The compound's planar structure enhances π-π stacking interactions, influencing its aggregation behavior in solution. Additionally, the presence of functional groups allows for versatile coordination with metal catalysts, potentially altering reaction mechanisms and enhancing selectivity in synthetic applications. | ||||||
NSC697923 | 343351-67-7 | sc-391107 sc-391107A | 1 mg 5 mg | $15.00 $51.00 | 3 | |
NSC697923, a furan derivative, exhibits intriguing electronic properties due to its conjugated system, which promotes unique charge transfer interactions. Its structural rigidity contributes to enhanced stability under various conditions, while the presence of substituents can modulate its reactivity. The compound's ability to engage in cycloaddition reactions highlights its potential for forming complex molecular architectures, making it a subject of interest in synthetic chemistry. | ||||||
PPQ-102 | 931706-15-9 | sc-364673 | 10 mg | $298.00 | 1 | |
PPQ-102, a furan derivative, showcases remarkable reactivity as an acid halide, facilitating nucleophilic acyl substitution with high efficiency. Its electron-rich furan ring enhances electrophilicity, allowing for rapid interactions with various nucleophiles. The compound's unique steric and electronic properties enable selective pathways in polymerization reactions, while its ability to form stable intermediates contributes to its versatility in synthetic applications. | ||||||
YC-1 | 170632-47-0 | sc-202856 sc-202856A sc-202856B sc-202856C | 1 mg 5 mg 10 mg 50 mg | $32.00 $122.00 $214.00 $928.00 | 9 | |
YC-1, a furan compound, exhibits intriguing reactivity patterns as an acid halide, characterized by its ability to engage in rapid electrophilic reactions. The presence of the furan moiety enhances its susceptibility to nucleophilic attack, leading to diverse reaction pathways. Its distinct electronic structure promotes unique intermolecular interactions, influencing reaction kinetics and enabling the formation of complex adducts. This behavior underscores its potential in various synthetic transformations. | ||||||
Kahweol | 6894-43-5 | sc-203089B sc-203089 sc-203089A | 5 mg 10 mg 25 mg | $88.00 $153.00 $357.00 | 9 | |
Kahweol, a furan derivative, showcases remarkable reactivity as an acid halide, primarily due to its electron-rich furan ring. This structure facilitates unique resonance stabilization, allowing for selective electrophilic substitutions. Its ability to form stable intermediates enhances reaction rates, while the steric properties of its substituents influence the regioselectivity of nucleophilic attacks. These characteristics contribute to its versatility in synthetic organic chemistry. | ||||||
PYR 41 | 418805-02-4 | sc-362786 sc-362786A | 5 mg 25 mg | $72.00 $153.00 | 1 | |
PYR 41, a furan-based compound, exhibits intriguing reactivity patterns as an acid halide, driven by its conjugated π-electron system. This configuration promotes strong dipole interactions, enhancing its electrophilic character. The compound's unique steric environment allows for diverse reaction pathways, leading to varied product distributions. Additionally, its solubility in polar solvents influences reaction kinetics, making it a notable candidate for exploring novel synthetic routes. | ||||||
DAR-4M AM | sc-221530 | 1 mg | $1199.00 | 3 | ||
DAR-4M AM, a furan derivative, showcases remarkable reactivity as an acid halide, characterized by its electron-rich furan ring that facilitates nucleophilic attack. The compound's planar structure and resonance stabilization contribute to its selective reactivity, allowing for efficient formation of acylation products. Its ability to engage in rapid intermolecular interactions enhances reaction rates, while its compatibility with various solvents opens avenues for innovative synthetic methodologies. | ||||||
Cafestol | 469-83-0 | sc-204663 | 50 mg | $260.00 | 4 | |
Cafestol, a furan compound, exhibits intriguing properties as an acid halide, primarily due to its unique electronic configuration. The presence of multiple functional groups allows for diverse reaction pathways, promoting selective acylation reactions. Its steric hindrance influences reaction kinetics, leading to distinct product distributions. Additionally, Cafestol's solubility in organic solvents enhances its versatility in synthetic applications, making it a valuable intermediate in organic chemistry. | ||||||
(+)-O,O′-Diacetyl-L-tartaric anhydride | 6283-74-5 | sc-250604 | 25 g | $97.00 | ||
(+)-O,O'-Diacetyl-L-tartaric anhydride, a furan derivative, showcases remarkable reactivity as an acid halide, characterized by its ability to form stable intermediates through intramolecular interactions. The compound's unique stereochemistry facilitates regioselective acylation, while its anhydride functionality promotes rapid esterification reactions. Its polar nature enhances solvation dynamics, influencing reaction rates and product formation in various organic transformations. |