Amino Alcohols
Items 31 to 40 of 491 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
MMP-2/MMP-9 Inhibitor II | 193807-60-2 | sc-311430 | 1 mg | $299.00 | 3 | |
MMP-2/MMP-9 Inhibitor II is an amino alcohol characterized by its ability to selectively modulate matrix metalloproteinase activity. Its unique structure facilitates specific interactions with enzyme active sites, leading to altered reaction kinetics. The compound exhibits strong polar characteristics due to its hydroxyl group, promoting solvation and enhancing its reactivity in various chemical contexts. Additionally, its conformation allows for effective steric hindrance, influencing binding affinity and selectivity. | ||||||
NH2-Et-OtBu Hydrochloride | 335598-67-9 | sc-286583 sc-286583A | 5 g 25 g | $390.00 $1575.00 | ||
NH2-Et-OtBu Hydrochloride is an amino alcohol distinguished by its capacity to engage in hydrogen bonding, which enhances its solubility in polar solvents. The presence of the bulky tert-butyl group contributes to steric effects, influencing its reactivity and selectivity in nucleophilic substitution reactions. This compound's unique electronic distribution allows for effective stabilization of transition states, thereby impacting reaction kinetics and pathways in various chemical environments. | ||||||
N,N-Bis[2-(p-tolylsulfonyloxy)ethyl]-p-toluenesulfonamide | 16695-22-0 | sc-250497 | 50 g | $99.00 | ||
N,N-Bis[2-(p-tolylsulfonyloxy)ethyl]-p-toluenesulfonamide is an amino alcohol characterized by its dual sulfonyl functionalities, which facilitate strong dipole-dipole interactions. This compound exhibits unique reactivity due to its ability to form stable intermediates in nucleophilic addition reactions. The presence of the p-tolyl groups enhances its hydrophobic character, influencing solubility and reactivity in non-polar environments, while also affecting its interaction with various substrates. | ||||||
SKF 83959 | 67287-95-0 | sc-204285 sc-204285A | 10 mg 50 mg | $183.00 $771.00 | ||
SKF 83959 is an amino alcohol notable for its intricate hydrogen bonding capabilities, which enhance its solubility in polar solvents. This compound exhibits unique reactivity patterns, particularly in its ability to participate in intramolecular interactions that stabilize transition states during chemical reactions. Its structural features promote specific molecular conformations, influencing reaction kinetics and selectivity in various chemical pathways, making it a subject of interest in synthetic chemistry. | ||||||
NNGH | 161314-17-6 | sc-222075 | 5 mg | $95.00 | 2 | |
NNGH is an amino alcohol characterized by its versatile functional groups that facilitate diverse intermolecular interactions, particularly through hydrogen bonding and dipole-dipole interactions. This compound demonstrates unique reactivity, allowing it to engage in nucleophilic attacks and form stable intermediates. Its ability to stabilize reactive species enhances its role in catalysis, influencing reaction rates and pathways, making it a fascinating subject for studies in organic synthesis and reaction mechanisms. | ||||||
1′-Hydroxy Bufuralol-d9 (Mixture of Diastereomers) | 1185069-74-2 | sc-213561 sc-213561A sc-213561B sc-213561C | 500 µg 5 mg 10 mg 25 mg | $816.00 $5406.00 $10537.00 $21410.00 | ||
1'-Hydroxy Bufuralol-d9 (Mixture of Diastereomers) is an amino alcohol notable for its chiral centers, which contribute to its distinct stereochemical properties. This compound exhibits strong hydrogen bonding capabilities, influencing solubility and reactivity in various environments. Its diastereomeric nature allows for differential interactions with substrates, potentially leading to unique reaction pathways and selectivity in synthetic applications. The compound's structural features also promote specific conformational dynamics, impacting its overall behavior in chemical reactions. | ||||||
(−)-Epinephrine | 51-43-4 | sc-205674 sc-205674A sc-205674B sc-205674C sc-205674D | 1 g 5 g 10 g 100 g 1 kg | $40.00 $102.00 $197.00 $1739.00 $16325.00 | ||
(-)-Epinephrine, an amino alcohol, is characterized by its catechol structure, which facilitates extensive hydrogen bonding and pi-stacking interactions. These features enhance its solubility in polar solvents and influence its reactivity in biochemical pathways. The compound's ability to engage in rapid conformational changes allows it to participate in diverse reaction mechanisms, while its chiral nature contributes to selective interactions with biological targets, affecting kinetic profiles in various systems. | ||||||
(R)-(−)-Phenylephrine hydrochloride | 61-76-7 | sc-203677 sc-203677A | 100 mg 5 g | $49.00 $65.00 | 1 | |
(R)-(-)-Phenylephrine hydrochloride, an amino alcohol, exhibits a unique stereochemistry that influences its molecular interactions, particularly through hydrogen bonding and dipole-dipole interactions. Its aromatic ring enhances π-π stacking, promoting stability in solution. The compound's chiral configuration allows for specific interactions with receptors, leading to distinct kinetic behaviors in various environments. Additionally, its solubility characteristics facilitate diverse reaction pathways, making it a versatile participant in chemical processes. | ||||||
Amino-2-propanol | 78-96-6 | sc-239223 | 100 ml | $36.00 | ||
Amino-2-propanol, an amino alcohol, exhibits notable steric hindrance due to its branched structure, which influences its reactivity in nucleophilic substitution reactions. The presence of both amino and hydroxyl functional groups allows for versatile hydrogen bonding, enhancing its solubility in various solvents. This compound can also engage in intramolecular interactions, leading to unique conformational dynamics that affect its behavior in catalytic processes and polymerization reactions. | ||||||
Choline dihydrogencitrate salt | 77-91-8 | sc-252600 | 1 kg | $86.00 | ||
Choline dihydrogencitrate salt, classified as an amino alcohol, showcases intriguing solvation dynamics due to its ionic nature, which enhances its interaction with polar solvents. The presence of multiple hydroxyl groups facilitates extensive hydrogen bonding, influencing its reactivity and stability in various environments. This compound also participates in unique coordination chemistry, allowing it to form complexes with metal ions, thereby altering its kinetic profiles in different reaction conditions. | ||||||