Amino Alcohols
Items 171 to 180 of 490 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
(R)-(−)-2-Amino-1-phenylethanol | 2549-14-6 | sc-250844 | 1 g | $148.00 | ||
(R)-(-)-2-Amino-1-phenylethanol, an amino alcohol, showcases distinctive characteristics stemming from its chiral center and functional groups. The presence of both an amino and a hydroxyl group allows for robust intramolecular hydrogen bonding, which stabilizes its conformation. This compound participates in nucleophilic addition reactions, where its reactivity is influenced by steric and electronic factors, making it a key player in asymmetric synthesis and catalysis. | ||||||
(S)-(+)-2-Amino-1-propanol | 2749-11-3 | sc-255565 | 1 g | $40.00 | ||
(S)-(+)-2-Amino-1-propanol, an amino alcohol, exhibits unique properties due to its chiral configuration and the presence of both an amino and hydroxyl group. This compound engages in strong intermolecular hydrogen bonding, enhancing its solubility in polar solvents. Its reactivity is characterized by the ability to act as a nucleophile in various organic reactions, facilitating the formation of diverse carbon-nitrogen bonds. Additionally, its stereochemistry plays a crucial role in influencing reaction pathways and selectivity. | ||||||
(R)-(−)-1-Amino-2-propanol | 2799-16-8 | sc-255458 | 1 g | $63.00 | ||
(R)-(-)-1-Amino-2-propanol, an amino alcohol, features a chiral center that imparts distinct stereochemical properties, influencing its reactivity in asymmetric synthesis. The compound's hydroxyl and amino groups enable robust hydrogen bonding, which enhances its solvation dynamics in polar environments. Its nucleophilic character allows it to participate in diverse reactions, including alkylation and acylation, while its unique spatial arrangement can affect reaction kinetics and product distribution. | ||||||
(S)-(+)-1-Amino-2-propanol | 2799-17-9 | sc-250934 | 1 g | $59.00 | ||
(S)-(+)-1-Amino-2-propanol, an amino alcohol, exhibits unique stereochemical properties due to its chiral configuration, which can significantly influence its role in catalytic processes. The compound's dual functional groups facilitate strong intermolecular interactions, enhancing its solubility in various solvents. Its ability to act as a nucleophile allows for participation in diverse organic transformations, while its specific spatial orientation can modulate reaction pathways and selectivity in synthetic applications. | ||||||
Metaproterenol hemisulfate salt | 5874-97-5 | sc-257701 | 1 g | $600.00 | 2 | |
Metaproterenol hemisulfate salt, classified as an amino alcohol, exhibits intriguing solubility characteristics due to its ionic nature, which facilitates interactions with polar solvents. The presence of the hemisulfate moiety enhances its ability to form strong hydrogen bonds, influencing its stability in solution. This compound can participate in unique electrostatic interactions, potentially affecting its reactivity and selectivity in various chemical environments, thereby impacting reaction dynamics. | ||||||
3-(Dibenzylamino)-1-propanol | 3161-51-1 | sc-231361 | 1 g | $82.00 | ||
3-(Dibenzylamino)-1-propanol, an amino alcohol, features a distinctive dibenzylamino group that enhances its steric bulk and electronic properties, influencing its reactivity in organic synthesis. The compound's ability to form hydrogen bonds and engage in π-π stacking interactions with aromatic systems can lead to unique stabilization effects in reaction intermediates. Its structural complexity allows for selective interactions in catalytic cycles, potentially altering reaction kinetics and pathways. | ||||||
3-Dimethylamino-1-propanol | 3179-63-3 | sc-238533 sc-238533A | 100 ml 500 ml | $151.00 $408.00 | ||
3-Dimethylamino-1-propanol, an amino alcohol, showcases notable reactivity due to its tertiary amine structure, which allows for rapid nucleophilic attacks in various organic reactions. Its ability to engage in hydrogen bonding enhances its solvation properties, promoting effective interactions with both polar and nonpolar solvents. The compound's steric hindrance from the dimethyl groups influences its kinetic behavior, potentially altering reaction pathways and selectivity in synthetic applications. | ||||||
N,N-Bis(2-hydroxyethyl)ethylenediamine | 3197-06-6 | sc-236103 | 1 g | $150.00 | ||
N,N-Bis(2-hydroxyethyl)ethylenediamine, an amino alcohol, exhibits unique chelating properties due to its dual hydroxyl and amine functionalities, enabling it to form stable complexes with metal ions. This compound's ability to participate in intramolecular hydrogen bonding can influence its conformational flexibility, affecting reactivity and solubility in various environments. Additionally, its bifunctional nature allows for diverse pathways in condensation reactions, enhancing its role in polymerization processes. | ||||||
6-Amino-1-hexanol | 4048-33-3 | sc-299944 sc-299944A | 5 g 25 g | $61.00 $182.00 | ||
6-Amino-1-hexanol, an amino alcohol, features a primary amine and a hydroxyl group, facilitating strong intermolecular hydrogen bonding that enhances its solubility in polar solvents. This compound can engage in nucleophilic substitution reactions, making it a versatile intermediate in organic synthesis. Its unique chain length contributes to distinct steric effects, influencing reaction kinetics and selectivity in various chemical transformations. | ||||||
DL-2-Amino-1-pentanol | 4146-04-7 | sc-234803 sc-234803A | 1 g 10 g | $70.00 $306.00 | ||
DL-2-Amino-1-pentanol, an amino alcohol, possesses both a primary amine and a hydroxyl group, enabling robust hydrogen bonding interactions that significantly enhance its solubility in aqueous environments. This compound can participate in diverse chemical reactions, including condensation and esterification, due to its reactive functional groups. Its unique five-carbon chain structure introduces specific steric and electronic effects, influencing reactivity and selectivity in synthetic pathways. | ||||||