Items 111 to 120 of 295 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
2-Tributylstannylthiazole | 121359-48-6 | sc-251803 | 1 g | $142.00 | ||
2-Tributylstannylthiazole is an organotin compound characterized by its thiazole ring, which introduces notable electronic properties and enhances its reactivity. The presence of the tributylstannyl group significantly increases its nucleophilic character, allowing for efficient interactions with electrophiles. This compound exhibits unique coordination behavior, influenced by the thiazole's heteroatoms, which can stabilize intermediates in various organometallic reactions. Additionally, the steric effects of the tributyl groups can modulate its reactivity and selectivity in synthetic pathways. | ||||||
Ethyl-5-(tributylstannyl)isoxazole-3-carboxylate | 126085-91-4 | sc-235079 | 500 mg | $235.00 | ||
Ethyl-5-(tributylstannyl)isoxazole-3-carboxylate is an organotin compound featuring an isoxazole moiety that imparts distinctive electronic characteristics, enhancing its reactivity. The tributylstannyl group contributes to its strong nucleophilicity, facilitating interactions with electrophiles. This compound exhibits unique coordination dynamics, influenced by the isoxazole's nitrogen and oxygen atoms, which can stabilize reactive intermediates. Its steric bulk also plays a crucial role in dictating reaction pathways and selectivity in organometallic transformations. | ||||||
2-Tributylstannylbenzo[b]thiophene | 148961-88-0 | sc-230688 | 1 g | $100.00 | ||
2-Tributylstannylbenzo[b]thiophene is an organotin compound characterized by its thiophene ring, which enhances its electronic properties and reactivity. The presence of the tributylstannyl group significantly increases its nucleophilicity, allowing for effective interactions with various electrophiles. This compound exhibits unique coordination behavior due to the sulfur atom in the thiophene, influencing reaction kinetics and selectivity in organometallic reactions. Its steric effects also modulate the accessibility of reactive sites, impacting overall reactivity. | ||||||
2-Chloro-5-(tributylstannyl)pyrimidine | 155191-68-7 | sc-225288 | 500 mg | $106.00 | ||
2-Chloro-5-(tributylstannyl)pyrimidine is an organotin compound notable for its pyrimidine core, which contributes to its unique electronic characteristics and reactivity. The chlorinated position enhances its electrophilic nature, facilitating nucleophilic attack by the tributylstannyl group. This compound exhibits distinctive coordination dynamics, allowing for selective interactions in organometallic transformations. Its steric bulk influences reaction pathways, optimizing reactivity and selectivity in various chemical environments. | ||||||
2-Fluoro-3-(tributylstannyl)pyridine | 155533-81-6 | sc-225361 | 1 g | $168.00 | ||
2-Fluoro-3-(tributylstannyl)pyridine is an organotin compound characterized by its pyridine framework, which imparts unique electronic properties and reactivity. The presence of the fluorine atom enhances its electrophilic character, promoting specific interactions with nucleophiles. This compound exhibits remarkable stability in organometallic reactions, with the tributylstannyl group providing significant steric hindrance that influences reaction kinetics and selectivity, enabling tailored pathways in synthetic applications. | ||||||
4-Bromo-2-(tributylstannyl)thiazole | 173978-98-8 | sc-232428 | 500 mg | $113.00 | ||
4-Bromo-2-(tributylstannyl)thiazole is an organotin compound featuring a thiazole ring that contributes to its distinctive reactivity and coordination properties. The bromine substituent enhances its electrophilic nature, facilitating interactions with various nucleophiles. This compound demonstrates notable stability in organometallic transformations, with the tributylstannyl group offering substantial steric protection, thereby modulating reaction rates and selectivity in synthetic pathways. | ||||||
6-Methoxy-2-(tributylstannyl)pyrimidine | 850501-35-8 | sc-233605 | 500 mg | $99.00 | ||
6-Methoxy-2-(tributylstannyl)pyrimidine is an organotin compound notable for its unique electronic properties and steric effects due to the tributylstannyl group. This compound exhibits significant coordination capabilities, allowing it to engage in diverse interactions with nucleophiles. Its pyrimidine ring contributes to enhanced stability and reactivity, facilitating unique pathways in cross-coupling reactions. The presence of the methoxy group further modulates its electronic environment, influencing reaction rates and selectivity in organometallic transformations. | ||||||
Zirconium(IV) propoxide solution | 23519-77-9 | sc-253855 sc-253855A | 100 ml 500 ml | $61.00 $167.00 | ||
Zirconium(IV) propoxide solution is a versatile precursor in materials science, characterized by its ability to form strong metal-oxygen bonds. This compound exhibits unique hydrolysis behavior, leading to the formation of zirconia nanoparticles through controlled gelation processes. Its reactivity is influenced by the presence of propoxide ligands, which facilitate the formation of stable complexes with various substrates. The solution's viscosity and surface tension properties enhance its applicability in sol-gel processes and thin-film deposition. | ||||||
Zinc Carbonate | 5263-02-5 | sc-296859 sc-296859A | 100 g 500 g | $92.00 $383.00 | ||
Zinc carbonate is a notable compound in the realm of metal carbonates, exhibiting a unique ability to undergo thermal decomposition, releasing carbon dioxide and forming zinc oxide. This transformation is influenced by its crystalline structure, which affects reaction kinetics and stability. The compound also demonstrates amphoteric behavior, reacting with both acids and bases, which allows for diverse interactions in various chemical environments. Its solubility characteristics further enhance its role in various applications. | ||||||
Strontium | 7440-24-6 | sc-253606 | 5 g | $53.00 | ||
Strontium is a reactive alkaline earth metal known for its striking luminescence when burned, producing a bright red flame. It readily forms alloys and compounds, exhibiting a tendency to react with water, albeit more slowly than its lighter counterparts. Strontium's unique electron configuration allows it to form stable complexes with various ligands, influencing its reactivity and interaction pathways. Its metallic properties include high density and malleability, making it distinct among metals. | ||||||