Amino Alcohols
Items 301 to 310 of 489 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
(S)-(-)-2-(Boc-amino)-3-cyclohexyl-1-propanol | 103322-56-1 | sc-253467 | 1 g | $115.00 | ||
(S)-(-)-2-(Boc-amino)-3-cyclohexyl-1-propanol is an amino alcohol notable for its chiral center and cyclohexyl group, which contribute to its unique steric and electronic properties. The Boc group not only provides protection but also influences the compound's solubility and reactivity. Its secondary alcohol functionality allows for diverse hydrogen bonding patterns, facilitating specific interactions in catalytic processes and enhancing selectivity in asymmetric synthesis. | ||||||
(R)-2-(Boc-amino)-1-propanol | 106391-86-0 | sc-258078 | 5 g | $137.00 | ||
(R)-2-(Boc-amino)-1-propanol is an amino alcohol characterized by its chiral configuration and the presence of a Boc protecting group, which modulates its reactivity and stability. The primary alcohol functionality enables it to participate in various hydrogen bonding interactions, influencing solubility and reactivity in different solvents. Its unique stereochemistry can lead to distinct reaction pathways, enhancing selectivity in synthetic applications and promoting specific molecular interactions. | ||||||
Boc-D-valinol | 106391-87-1 | sc-223836 | 1 g | $60.00 | ||
Boc-D-valinol is a chiral amino alcohol featuring a tert-butoxycarbonyl (Boc) protecting group that enhances its stability and reactivity. The presence of the hydroxyl group allows for strong hydrogen bonding, which can significantly affect its solubility in polar and non-polar solvents. Its stereochemical properties facilitate unique reaction kinetics, enabling selective transformations and influencing the formation of intermediates in synthetic pathways. | ||||||
Boc-D-phenylalaninol | 106454-69-7 | sc-257174 | 1 g | $72.00 | ||
Boc-D-phenylalaninol is a chiral amino alcohol characterized by its tert-butoxycarbonyl (Boc) protective group, which imparts enhanced stability. The aromatic side chain contributes to unique π-π stacking interactions, influencing its solubility and reactivity in various environments. This compound exhibits distinct stereoelectronic effects, which can modulate reaction pathways and kinetics, allowing for selective functionalization in synthetic organic chemistry. | ||||||
N-Boc-(2S,3S)-(-)-2-amino-3-methyl-1-pentanol | 106946-74-1 | sc-228670 | 2 g | $70.00 | ||
N-Boc-(2S,3S)-(-)-2-amino-3-methyl-1-pentanol is a chiral amino alcohol featuring a tert-butoxycarbonyl (Boc) group that enhances its stability and solubility. The presence of a branched alkyl chain introduces steric hindrance, influencing its reactivity and selectivity in nucleophilic reactions. This compound's unique stereochemistry allows for specific interactions with electrophiles, facilitating tailored synthetic pathways and optimizing reaction conditions in organic synthesis. | ||||||
(R)-(-)-2-Benzylamino-1-phenylethanol | 107171-75-5 | sc-229044 | 1 g | $127.00 | ||
(R)-(-)-2-Benzylamino-1-phenylethanol is a chiral amino alcohol characterized by its aromatic benzyl and phenyl groups, which contribute to its unique electronic properties and steric effects. These features enhance its ability to engage in hydrogen bonding and π-π stacking interactions, influencing its solubility and reactivity. The compound exhibits distinct kinetic behavior in nucleophilic substitution reactions, allowing for selective transformations in synthetic organic chemistry. | ||||||
N-Boc-L-cyclohexylglycinol | 107202-39-1 | sc-228691 | 1 g | $59.00 | ||
N-Boc-L-cyclohexylglycinol is a chiral amino alcohol notable for its cyclohexyl group, which imparts significant steric hindrance and influences its conformational flexibility. This compound exhibits unique hydrogen bonding capabilities due to its Boc (tert-butyloxycarbonyl) protecting group, enhancing its stability in various reaction environments. Its distinct molecular interactions facilitate selective reactivity in asymmetric synthesis, making it a versatile intermediate in organic transformations. | ||||||
N-(Benzyloxycarbonyl)-3-amino-1,2-propanediol | 108587-40-2 | sc-228643 | 25 g | $121.00 | ||
N-(Benzyloxycarbonyl)-3-amino-1,2-propanediol is a chiral amino alcohol characterized by its benzyloxycarbonyl (Z) protecting group, which enhances its reactivity and solubility in polar solvents. The presence of the hydroxyl and amino groups allows for strong intramolecular hydrogen bonding, influencing its conformational dynamics. This compound's unique steric and electronic properties enable it to participate in selective nucleophilic reactions, making it a valuable intermediate in synthetic organic chemistry. | ||||||
(S)-(+)-2-(N,N-Dibenzylamino)-4-methylpentanol | 111060-53-8 | sc-229214 | 5 g | $87.00 | ||
(S)-(+)-2-(N,N-Dibenzylamino)-4-methylpentanol is a chiral amino alcohol notable for its dual functional groups, which facilitate diverse intermolecular interactions. The dibenzylamino moiety enhances its lipophilicity, promoting solubility in organic solvents. Its unique stereochemistry allows for specific chiral recognition in reactions, while the hydroxyl group can engage in hydrogen bonding, influencing reaction pathways and kinetics in various organic transformations. | ||||||
(S)-2-(N,N-Dibenzylamino)-3-methylbutanol | 111060-54-9 | sc-229247 | 5 g | $93.00 | ||
(S)-2-(N,N-Dibenzylamino)-3-methylbutanol is a chiral amino alcohol characterized by its unique structural features that enable selective molecular interactions. The presence of the dibenzylamino group contributes to its hydrophobic character, enhancing its affinity for non-polar environments. This compound's stereogenic center plays a crucial role in asymmetric synthesis, allowing for tailored reactivity and selectivity in catalytic processes, while the hydroxyl group facilitates intramolecular hydrogen bonding, impacting its conformational dynamics. | ||||||