Chiral Reagents
Items 111 to 120 of 464 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
2-Methylisoborneol solution | 2371-42-8 | sc-251786 | 1 ml | $395.00 | ||
2-Methylisoborneol solution acts as a chiral reagent, characterized by its unique bicyclic structure that facilitates specific molecular interactions. Its conformational flexibility allows for tailored binding with substrates, enhancing enantioselectivity in reactions. The compound's hydrophobic nature influences solubility and reactivity, while its ability to participate in non-covalent interactions, such as van der Waals forces, plays a crucial role in directing reaction pathways and optimizing yields. | ||||||
(S)-Ketorolac | 66635-92-5 | sc-208368 | 5 mg | $430.00 | ||
(S)-Ketorolac acts as a chiral reagent characterized by its ability to form strong non-covalent interactions, such as hydrogen bonds and dipole-dipole interactions, which enhance enantioselectivity in various reactions. Its unique stereochemistry allows for specific spatial orientation, promoting favorable transition states. Additionally, the presence of functional groups influences reactivity and selectivity, making it a valuable tool in asymmetric synthesis and chiral resolution processes. | ||||||
(R)-Ketorolac | 66635-93-6 | sc-208241 | 5 mg | $375.00 | ||
(R)-Ketorolac serves as a chiral reagent distinguished by its capacity to stabilize transition states through specific steric interactions and favorable electronic environments. Its unique chiral center facilitates selective binding to substrates, enhancing reaction rates and enantioselectivity. The compound's functional groups contribute to its reactivity profile, allowing for tailored approaches in asymmetric synthesis and enabling efficient chiral discrimination in complex reaction pathways. | ||||||
(S)-(−)-α-Amino-γ-butyrolactone hydrobromide | 15295-77-9 | sc-253483 | 1 g | $42.00 | ||
(S)-(-)-α-Amino-γ-butyrolactone hydrobromide acts as a chiral reagent, characterized by its cyclic structure that facilitates unique stereochemical interactions. This compound exhibits strong hydrogen bonding capabilities, enhancing its reactivity in asymmetric synthesis. Its ability to stabilize transition states through specific molecular interactions leads to improved enantioselectivity. Additionally, the presence of the hydrobromide salt form influences solubility and reactivity profiles, optimizing reaction conditions. | ||||||
Abamectin | 71751-41-2 | sc-207239 | 100 mg | $136.00 | 1 | |
Abamectin serves as a chiral reagent, notable for its ability to engage in selective molecular interactions due to its unique stereochemistry. Its structure allows for the formation of specific chiral environments that can influence reaction pathways and enhance enantioselectivity. The compound's distinct electronic distribution and steric hindrance contribute to its reactivity, facilitating the formation of preferred transition states in asymmetric synthesis, thereby optimizing reaction outcomes. | ||||||
D-α-Hydroxyisovaleric acid | 17407-56-6 | sc-239638 | 1 g | $158.00 | ||
D-α-Hydroxyisovaleric acid serves as a chiral reagent, notable for its ability to form stable complexes with metal catalysts, enhancing enantioselectivity in various reactions. Its hydroxyl group participates in intramolecular hydrogen bonding, which can influence reaction pathways and kinetics. The compound's unique steric environment allows for selective interactions with substrates, promoting desired stereochemical outcomes in asymmetric transformations. | ||||||
(S)-(−)-Indoline-2-carboxylic acid | 79815-20-6 | sc-255553 | 1 g | $31.00 | ||
(S)-(-)-Indoline-2-carboxylic acid acts as a chiral reagent, distinguished by its ability to stabilize transition states through hydrogen bonding and π-π stacking interactions. Its unique conformation promotes selective binding with substrates, enhancing enantioselectivity in asymmetric reactions. The compound's carboxylic acid functionality can also participate in intramolecular interactions, influencing reaction kinetics and leading to improved yields in chiral synthesis. | ||||||
Fosinoprilat Disodium Salt | 95399-71-6 | sc-207700 | 5 mg | $380.00 | ||
Fosinoprilat Disodium Salt serves as a chiral reagent, characterized by its capacity to form stable complexes with metal catalysts, enhancing enantioselectivity in asymmetric transformations. Its unique stereochemistry allows for specific interactions with substrates, facilitating selective pathways in reactions. The compound's ionic nature contributes to solubility and reactivity, promoting efficient reaction kinetics and improved selectivity in chiral synthesis processes. | ||||||
(R)-(+)-Citronellic acid | 18951-85-4 | sc-229089 | 5 g | $183.00 | ||
(R)-(+)-Citronellic acid is a chiral reagent distinguished by its ability to engage in specific hydrogen bonding interactions, which can modulate reaction dynamics. Its unique stereochemistry facilitates selective coordination with transition metal complexes, enhancing enantioselectivity in catalytic processes. The compound's carboxylic acid functionality can also participate in esterification reactions, influencing the formation of chiral products through distinct mechanistic pathways. | ||||||
N-Benzylquininium chloride | 67174-25-8 | sc-236010 | 5 g | $91.00 | ||
N-Benzylquininium chloride serves as a chiral reagent distinguished by its ability to facilitate enantioselective transformations through unique electrostatic interactions. The presence of the quaternary ammonium moiety enhances its solubility in polar solvents, promoting effective substrate alignment. Its sterically demanding structure influences transition state stabilization, thereby modulating reaction kinetics. This compound's capacity to form chiral environments makes it a valuable tool in asymmetric synthesis. | ||||||