Amino Alcohols
Items 251 to 260 of 490 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
1-Cyclopentylethanol | 52829-98-8 | sc-224637 | 2 g | $89.00 | ||
1-Cyclopentylethanol, classified as an amino alcohol, features a cyclopentyl group that introduces unique steric effects, influencing its reactivity and interaction with other molecules. The hydroxyl and amino functionalities enable robust hydrogen bonding, which can stabilize transition states in reactions. Its distinct conformation allows for selective interactions in catalytic processes, potentially enhancing reaction rates and selectivity in organic synthesis. | ||||||
(R)-(−)-Leucinol | 53448-09-2 | sc-253414 | 1 g | $52.00 | ||
(R)-(−)-Leucinol, an amino alcohol, exhibits intriguing stereochemistry that influences its molecular interactions. The presence of both hydroxyl and amino groups facilitates strong hydrogen bonding, enhancing solubility in polar solvents. Its chiral nature allows for specific interactions with enzymes and receptors, potentially affecting reaction pathways. Additionally, the compound's unique spatial arrangement can lead to distinct kinetic profiles in various chemical reactions, making it a subject of interest in synthetic chemistry. | ||||||
(S)-(+)-1-Dimethylamino-2-propanol | 53636-17-2 | sc-236750 sc-236750A | 250 mg 1 g | $159.00 $192.00 | ||
(S)-(+)-1-Dimethylamino-2-propanol, an amino alcohol, features a unique chiral center that significantly impacts its reactivity and interaction with other molecules. The dimethylamino group enhances nucleophilicity, promoting rapid reaction kinetics in nucleophilic substitution processes. Its ability to form stable hydrogen bonds with polar solvents increases solvation efficiency, while its steric configuration can influence the selectivity of reactions, making it a notable compound in organic synthesis. | ||||||
N-Benzyl-L-prolinol | 53912-80-4 | sc-257832 | 5 g | $79.00 | ||
N-Benzyl-L-prolinol, an amino alcohol, exhibits intriguing stereochemical properties due to its chiral proline backbone, which influences its conformational flexibility and molecular interactions. The benzyl group enhances lipophilicity, facilitating unique solvation dynamics in organic reactions. Its hydroxyl group can engage in strong hydrogen bonding, affecting reaction pathways and kinetics, while the proline structure may promote specific catalytic behaviors in asymmetric synthesis. | ||||||
2-(Ethylthio)ethylamine hydrochloride | 54303-30-9 | sc-225102 | 1 g | $65.00 | ||
2-(Ethylthio)ethylamine hydrochloride, an amino alcohol, features a unique ethylthio group that enhances its nucleophilicity, allowing for distinctive reactivity in substitution reactions. The presence of the amine and hydroxyl functionalities enables robust hydrogen bonding, influencing solubility and interaction with polar solvents. This compound's structural characteristics facilitate specific conformational arrangements, potentially impacting its role in various chemical transformations and reaction mechanisms. | ||||||
(S)-2-Amino-1-phenylethanol | 56613-81-1 | sc-229249 | 500 mg | $409.00 | ||
(S)-2-Amino-1-phenylethanol, an amino alcohol, exhibits intriguing stereochemistry that influences its reactivity and interaction with other molecules. The phenyl group contributes to its hydrophobic character, while the amino and hydroxyl groups enable strong hydrogen bonding, enhancing its solubility in polar solvents. This compound can participate in diverse reaction pathways, including nucleophilic attacks and condensation reactions, showcasing its versatility in organic synthesis. | ||||||
2-Methylaminomethyl-1,3-dioxolane | 57366-77-5 | sc-230540 | 5 g | $91.00 | ||
2-Methylaminomethyl-1,3-dioxolane, an amino alcohol, features a unique dioxolane ring that enhances its stability and reactivity. The presence of the methylamino group allows for effective hydrogen bonding, facilitating interactions with various substrates. Its structure promotes distinct reaction kinetics, enabling it to act as a nucleophile in diverse organic transformations. Additionally, the compound's polar characteristics contribute to its solubility in a range of solvents, influencing its behavior in synthetic applications. | ||||||
3-Iodobenzyl alcohol | 57455-06-8 | sc-231768 | 5 g | $64.00 | ||
3-Iodobenzyl alcohol, classified as an amino alcohol, exhibits intriguing properties due to its iodo substituent, which enhances its electrophilicity. This feature allows for selective nucleophilic attacks, making it a versatile intermediate in organic synthesis. The hydroxyl group contributes to strong hydrogen bonding, influencing solubility and reactivity in polar environments. Its unique molecular interactions facilitate diverse pathways in chemical reactions, showcasing its potential in various synthetic methodologies. | ||||||
(R)-(+)-2-Amino-3-benzyloxy-1-propanol | 58577-87-0 | sc-236581 | 1 g | $98.00 | ||
(R)-(+)-2-Amino-3-benzyloxy-1-propanol, an amino alcohol, showcases unique stereochemistry that influences its reactivity and interaction with other molecules. The benzyloxy group enhances lipophilicity, promoting solvation in organic solvents. Its amino group can engage in both hydrogen bonding and coordination with metal catalysts, facilitating various reaction pathways. This compound's distinct structural features enable it to participate in selective transformations, highlighting its role in complex organic synthesis. | ||||||
4-Chloro-N-(2-hydroxyethyl)-2-nitroaniline | 59320-13-7 | sc-232581 | 10 g | $75.00 | ||
4-Chloro-N-(2-hydroxyethyl)-2-nitroaniline, an amino alcohol, exhibits intriguing electronic properties due to the presence of both a nitro and a chloro substituent, which can influence its reactivity. The hydroxyl group allows for strong hydrogen bonding, enhancing solubility in polar solvents. Its unique structure facilitates nucleophilic attack in various reactions, while the nitro group can act as an electron-withdrawing moiety, modulating reaction kinetics and selectivity in synthetic pathways. | ||||||