Nitrogen Compounds
Items 231 to 240 of 351 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
N,N′-Bis(salicylidene)ethylenediaminocobalt(II) | 14167-18-1 | sc-228790 | 1 g | $63.00 | ||
N,N'-Bis(salicylidene)ethylenediaminocobalt(II) exhibits intriguing coordination chemistry due to its bidentate ligand structure, allowing for the formation of stable complexes with transition metals. The compound's chelating ability enhances its electron density, promoting unique redox behavior. Its planar geometry facilitates strong π-π interactions, while the presence of hydroxyl groups enables hydrogen bonding, influencing solubility and reactivity in diverse environments. | ||||||
2-Nitro-6-(trifluoromethyl)benzonitrile | 1227581-80-7 | sc-506582 | 1 g | $443.00 | ||
2-Nitro-6-(trifluoromethyl)benzonitrile exhibits intriguing electronic properties due to the presence of the trifluoromethyl group, which enhances its electrophilicity. The nitro substituent introduces significant resonance effects, facilitating diverse reaction mechanisms, including electrophilic aromatic substitution. Its strong dipole moment contributes to unique solvation dynamics, influencing reaction kinetics and selectivity in polar environments. This compound's distinct molecular interactions make it a versatile participant in synthetic pathways. | ||||||
2,4,6-Tri(9H-carbazol-9-yl)-1,3,5-triazine | 134984-37-5 | sc-476873 | 1 g | $273.00 | ||
2,4,6-Tri(9H-carbazol-9-yl)-1,3,5-triazine is a nitrogen-rich compound characterized by its extensive π-conjugation and robust electron-donating properties. The presence of multiple carbazole units enhances its photophysical behavior, leading to strong light absorption and emission. This structure facilitates unique intermolecular interactions, such as π-π stacking and hydrogen bonding, which can significantly influence its stability and reactivity in various chemical environments. | ||||||
3β-DOXYL-5α-cholestane, free radical | 55569-61-4 | sc-507269 | 5 mg | $300.00 | ||
Semustine | 13909-09-6 | sc-391062 | 100 mg | $114.00 | 1 | |
Semustine, a nitrogen-containing compound, showcases unique reactivity through its electrophilic nature, allowing it to engage in nucleophilic substitution reactions. Its structure promotes significant steric hindrance, which can influence reaction kinetics and selectivity. The presence of nitrogen atoms contributes to its ability to form hydrogen bonds, enhancing solubility in polar solvents. Additionally, its interactions with various nucleophiles can lead to diverse reaction pathways, making it a versatile compound in synthetic chemistry. | ||||||
Ethylenediaminetetraacetic acid tripotassium salt | 17572-97-3 | sc-269191 | 25 g | $56.00 | ||
Ethylenediaminetetraacetic acid tripotassium salt features a chelating structure that enables it to form stable complexes with metal ions, enhancing its role in various chemical environments. The tripotassium configuration provides increased solubility in aqueous solutions, facilitating effective ion coordination. Its ability to modulate metal ion availability can influence reaction kinetics, making it a key player in processes requiring precise metal ion control and stabilization. | ||||||
Cetyltrimethylammonium Bromide | 57-09-0 | sc-278833 sc-278833A sc-278833B sc-278833C | 100 g 250 g 1 kg 5 kg | $40.00 $80.00 $135.00 $585.00 | 3 | |
Cetyltrimethylammonium Bromide, as a nitrogenous compound, showcases remarkable surfactant properties due to its quaternary ammonium structure. This facilitates strong electrostatic interactions with anionic species, enhancing its ability to stabilize emulsions and foams. Its hydrophobic tail promotes micelle formation in aqueous environments, allowing for unique solubilization pathways. The compound's amphiphilic nature also influences its adsorption behavior at interfaces, impacting surface tension dynamics. | ||||||
UCL 1684 ditrifluoroacetate | 201147-19-5 | sc-253818 | 5 mg | $281.00 | 1 | |
UCL 1684 ditrifluoroacetate exhibits intriguing reactivity as an acid halide, characterized by its strong electrophilic nature. The presence of trifluoroacetate groups enhances its ability to engage in nucleophilic acyl substitution reactions, leading to rapid formation of acyl derivatives. Its unique steric and electronic properties facilitate selective interactions with nucleophiles, influencing reaction kinetics and pathways. Additionally, the compound's polar nature contributes to its solubility in various organic solvents, further expanding its reactivity profile. | ||||||
4-imino-2-mercapto-5-(4-phenyl-1,3-thiazol-2-yl)-3-azaspiro[5.5]undec-1-ene-1-carbonitrile | sc-352422 sc-352422A | 250 mg 1 g | $197.00 $399.00 | |||
4-imino-2-mercapto-5-(4-phenyl-1,3-thiazol-2-yl)-3-azaspiro[5.5]undec-1-ene-1-carbonitrile showcases remarkable reactivity due to its spirocyclic structure, which introduces strain and enhances nucleophilicity. The presence of the imino and mercapto groups facilitates diverse coordination interactions, allowing it to form stable complexes with transition metals. Its unique electronic distribution promotes selective electrophilic attack, influencing reaction pathways and kinetics in various chemical systems. | ||||||
2-Oxa-6-azaspiro[3.5]nonane-6-carboxylic acid tert-butyl ester | 1245816-29-8 | sc-506593 | 1 g | $432.00 | ||
2-Oxa-6-azaspiro[3.5]nonane-6-carboxylic acid tert-butyl ester showcases remarkable reactivity stemming from its spirocyclic architecture, which introduces steric hindrance and unique conformational dynamics. The tert-butyl ester group enhances lipophilicity, influencing solubility and reactivity in organic solvents. Its carboxylic acid moiety engages in nucleophilic acyl substitution, while the nitrogen atom can participate in coordination chemistry, affecting reaction kinetics and selectivity in diverse synthetic pathways. | ||||||