Amino Alcohols
Items 111 to 120 of 491 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
(1R,2R)-(−)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol | 716-61-0 | sc-223209 sc-223209A | 10 g 25 g | $89.00 $138.00 | ||
(1R,2R)-(-)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol is an amino alcohol characterized by its chiral centers and the presence of a nitrophenyl group, which enhances its electronic properties. This compound exhibits strong hydrogen bonding capabilities due to its hydroxyl and amino functionalities, influencing its solubility in polar solvents. Its unique structure allows for selective reactivity in condensation reactions, potentially leading to the formation of complex molecular architectures. | ||||||
5-Hydroxymethyl-2,2,5-trimethyl-1,3-dioxane | 3663-46-5 | sc-233377 | 1 g | $82.00 | ||
5-Hydroxymethyl-2,2,5-trimethyl-1,3-dioxane is an amino alcohol notable for its dioxane ring structure, which imparts unique steric hindrance and polarity. This compound exhibits significant hydrogen bonding potential, enhancing its solubility in polar solvents. Its molecular configuration allows for selective reactivity, particularly in nucleophilic addition reactions, and facilitates the formation of stable intermediates, influencing the kinetics of various organic transformations. | ||||||
(1S,2S)-(+)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol | 2964-48-9 | sc-225006 | 10 g | $89.00 | ||
(1S,2S)-(+)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol is an amino alcohol notable for its stereochemistry and the electron-withdrawing nitrophenyl moiety, which modulates its reactivity. The compound's dual functional groups facilitate intramolecular interactions, promoting unique conformational dynamics. Its ability to participate in nucleophilic substitutions and form stable intermediates makes it a versatile building block in organic synthesis, influencing reaction pathways and kinetics. | ||||||
2,2′-(4-Methylphenylimino)diethanol | 3077-12-1 | sc-238246 | 100 g | $63.00 | ||
2,2'-(4-Methylphenylimino)diethanol is an amino alcohol characterized by its unique imino linkage and the presence of a methylphenyl group, which enhances its steric and electronic properties. This compound exhibits strong hydrogen bonding capabilities, influencing solubility and reactivity in various solvents. Its structure allows for diverse intermolecular interactions, facilitating complexation with metal ions and participation in condensation reactions, thereby impacting reaction rates and mechanisms in synthetic pathways. | ||||||
2,3-Dimethoxybenzyl alcohol | 5653-67-8 | sc-230835 | 5 g | $33.00 | ||
2,3-Dimethoxybenzyl alcohol is an amino alcohol characterized by its methoxy substituents, which enhance its electron-donating properties and influence its reactivity. The presence of these groups allows for increased solvation in polar environments, promoting effective hydrogen bonding. This compound exhibits unique stereoelectronic effects that can modulate reaction pathways, particularly in electrophilic aromatic substitutions, leading to distinct kinetic profiles in organic synthesis. | ||||||
2,2-Bis(3-amino-4-hydroxyphenyl)hexafluoropropane | 83558-87-6 | sc-251804 | 5 g | $201.00 | ||
2,2-Bis(3-amino-4-hydroxyphenyl)hexafluoropropane, as an amino alcohol, showcases remarkable molecular versatility through its dual functional groups. The presence of multiple hydroxyl and amino groups facilitates extensive hydrogen bonding, enhancing its solubility and reactivity. This compound can engage in complex intermolecular interactions, influencing reaction kinetics and pathways. Its unique fluorinated structure may also impart distinctive electronic properties, affecting its behavior in various chemical environments. | ||||||
Bisoprolol | 66722-44-9 | sc-278792 | 25 mg | $204.00 | ||
Bisoprolol, an amino alcohol, exhibits intriguing molecular characteristics due to its specific stereochemistry, which influences its spatial orientation and reactivity. The compound's hydroxyl group enhances its ability to form hydrogen bonds, promoting solubility in aqueous environments. Its secondary amine functionality allows for unique interactions with electrophiles, potentially altering reaction pathways. The compound's distinct molecular structure also contributes to its stability and reactivity in various chemical contexts. | ||||||
Z-trans-4-Hydroxy-L-prolinol | 95687-41-5 | sc-255727 | 1 g | $179.00 | ||
Z-trans-4-Hydroxy-L-prolinol, classified as an amino alcohol, exhibits intriguing stereochemical properties due to its unique configuration. The hydroxyl group and the proline backbone enable it to participate in diverse hydrogen bonding networks, which can significantly alter its reactivity and stability in various solvents. Its ability to form stable intramolecular interactions may influence conformational dynamics, impacting reaction pathways and kinetics in organic synthesis. | ||||||
(+)-Nebivolol | 118457-15-1 | sc-212367 | 0.5 mg | $500.00 | ||
(+)–Nebivolol, an amino alcohol, features a chiral center that contributes to its distinct stereochemistry, allowing for specific interactions with biological macromolecules. Its secondary amine and hydroxyl functionalities facilitate robust hydrogen bonding, enhancing solubility in polar solvents. The compound's unique spatial arrangement can lead to selective reactivity, influencing its behavior in catalytic processes and potentially affecting reaction rates and mechanisms in synthetic applications. | ||||||
SR 58611A | 121524-09-2 | sc-361365 sc-361365A | 10 mg 50 mg | $206.00 $940.00 | ||
SR 58611A, an amino alcohol, exhibits intriguing properties due to its unique molecular structure. The presence of both hydroxyl and amine groups enables it to engage in diverse hydrogen bonding networks, which can significantly influence its solubility and reactivity. Its specific steric configuration allows for selective interactions with various substrates, potentially altering reaction pathways and kinetics. This compound's ability to stabilize transition states may enhance its role in catalytic systems, making it a subject of interest in synthetic chemistry. | ||||||