Amides
Items 81 to 86 of 86 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
2-(isopropylamino)acetamide hydrochloride | 85791-77-1 | sc-274005 | 250 mg | $119.00 | ||
2-(isopropylamino)acetamide hydrochloride exhibits intriguing properties as an amide, particularly due to its dual functional groups. The isopropylamino moiety introduces steric effects that can modulate reactivity, while the amide bond contributes to its capacity for intramolecular interactions. This compound can engage in hydrogen bonding, enhancing its solubility and reactivity in various solvents. Its hydrochloride form promotes ionic interactions, further influencing its behavior in chemical reactions. | ||||||
Tyrphostin B44, (+) enantiomer | 133550-37-5 | sc-203305 | 5 mg | $30.00 | ||
Tyrphostin B44, (+) enantiomer, is characterized by its unique amide functionality, which facilitates specific hydrogen bonding interactions. This compound exhibits notable stability in various solvents, allowing for diverse solvation dynamics. Its chiral nature influences reaction pathways, leading to enantioselective outcomes in certain conditions. Additionally, the presence of functional groups contributes to its ability to engage in complex molecular interactions, enhancing its reactivity profile in synthetic applications. | ||||||
3,4-dihydroxy Hydrocinnamic acid (L-Aspartic acid dibenzyl ester) amide | 615264-62-5 | sc-223562 sc-223562A sc-223562B sc-223562C | 5 mg 10 mg 50 mg 100 mg | $42.00 $106.00 $336.00 $588.00 | ||
3,4-Dihydroxy Hydrocinnamic acid (L-Aspartic acid dibenzyl ester) amide features a distinctive amide bond that contributes to its stability and reactivity. The presence of hydroxyl groups enhances its ability to engage in intramolecular hydrogen bonding, influencing its conformational flexibility. This compound can participate in unique reaction pathways, including acylation and amidation, which are facilitated by its sterically accessible functional groups, allowing for diverse synthetic applications. | ||||||
N-(2-aminophenyl)benzamide | 721-47-1 | sc-354257 sc-354257A | 1 g 5 g | $693.00 $2235.00 | ||
N-(2-aminophenyl)benzamide is characterized by its amide functional group, which promotes strong hydrogen bonding and dipole-dipole interactions. The presence of the aromatic rings enhances π-π stacking interactions, influencing its solubility and reactivity. This compound can engage in acylation reactions, showcasing distinct kinetics due to resonance stabilization. Its structural features allow for selective interactions in complexation processes, impacting its behavior in various chemical environments. | ||||||
Novobiocin Sodium Salt | 1476-53-5 | sc-358734 sc-358734A sc-358734B sc-358734C sc-358734D sc-358734E | 1 g 5 g 10 g 50 g 100 g 500 g | $84.00 $287.00 $350.00 $1200.00 $2283.00 $11223.00 | 1 | |
Novobiocin Sodium Salt, as an amide, showcases unique interactions through its ability to form hydrogen bonds, enhancing its solubility in aqueous environments. This compound exhibits distinct kinetic behavior, facilitating rapid binding to target sites. Its structural conformation allows for specific steric interactions, influencing molecular recognition processes. Additionally, the presence of sodium ions can alter its reactivity, promoting diverse pathways in complex biochemical systems. | ||||||
N-(5-Amino-2-methylphenyl)acetamide | 5434-30-0 | sc-330417 | 500 mg | $214.00 | ||
N-(5-Amino-2-methylphenyl)acetamide is an intriguing amide characterized by its capacity for intramolecular hydrogen bonding, which can stabilize its conformation and influence reactivity. The amino group enhances nucleophilicity, allowing for diverse reaction pathways, including acylation and amidation. Its aromatic structure contributes to π-π interactions, potentially affecting solubility and reactivity in various solvents, making it a versatile compound in organic synthesis. | ||||||