Chiral Reagents
Items 171 to 180 of 464 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
6-Epi Doxycycline | 3219-99-6 | sc-210513 | 1 mg | $456.00 | ||
6-Epi Doxycycline is a chiral reagent notable for its unique structural features, including a tetracyclic core that influences its reactivity. The presence of multiple functional groups allows for diverse intermolecular interactions, enhancing its ability to stabilize transition states. Its stereochemical configuration plays a crucial role in dictating reaction pathways, leading to selective outcomes in asymmetric synthesis. Additionally, its solubility characteristics can affect reaction conditions and kinetics, making it a versatile tool in chiral synthesis. | ||||||
(−)-Caryophyllene oxide | 1139-30-6 | sc-257221 | 1 g | $98.00 | 1 | |
(-)-Caryophyllene oxide serves as a versatile chiral reagent, characterized by its unique bicyclic structure that promotes specific stereochemical interactions. Its ability to form stable complexes with various transition metals enhances catalytic efficiency in asymmetric synthesis. The compound's distinct conformational flexibility allows for tailored reactivity, influencing selectivity in reaction pathways. Furthermore, its moderate polarity aids in solvation dynamics, optimizing chiral discrimination in diverse chemical environments. | ||||||
(S)-(+)-1,2-Propanediol | 4254-15-3 | sc-236755 | 5 g | $160.00 | ||
(S)-(+)-1,2-Propanediol serves as a chiral reagent characterized by its ability to form hydrogen bonds due to its hydroxyl groups, which can significantly influence reaction dynamics. Its unique stereochemistry facilitates selective interactions with substrates, promoting enantioselectivity in various reactions. The compound's viscosity and polarity enhance its solvation properties, impacting reaction rates and mechanisms, making it an effective agent in asymmetric transformations. | ||||||
Tranexamic acid | 1197-18-8 | sc-204921 sc-204921A | 5 g 10 g | $29.00 $50.00 | 10 | |
Tranexamic acid, a chiral reagent, exhibits a distinctive planar structure that allows for specific interactions with chiral catalysts and substrates. Its ability to form stable hydrogen bonds enhances selectivity in asymmetric synthesis. The compound's unique stereochemistry influences reaction kinetics, promoting efficient enantioselective transformations. Additionally, its moderate hydrophilicity affects solubility in polar solvents, facilitating diverse applications in chiral synthesis and catalysis. | ||||||
Epi-galanthamine | 1668-85-5 | sc-207625 | 5 mg | $380.00 | ||
Epi-galanthamine is a notable chiral reagent distinguished by its intricate stereochemical framework, which facilitates specific molecular interactions in asymmetric synthesis. Its unique arrangement allows for effective hydrogen bonding and steric hindrance, optimizing reaction pathways. The compound's ability to stabilize transition states enhances enantioselectivity, while its dynamic conformational flexibility contributes to varied reactivity profiles in diverse chemical environments. | ||||||
Cholesteryl chloroformate | 7144-08-3 | sc-239543 | 25 g | $55.00 | ||
Cholesteryl chloroformate serves as a chiral reagent, distinguished by its ability to form robust acylation intermediates through its reactive chloroformate group. This reactivity facilitates selective acylation of alcohols and amines, promoting unique stereochemical outcomes. The steric bulk of the cholesteryl moiety enhances the chiral environment, influencing reaction kinetics and selectivity. Its distinct molecular interactions contribute to the formation of enantioenriched products in asymmetric synthesis. | ||||||
cis-4-Hydroxy-D-proline | 2584-71-6 | sc-206064 sc-206064A | 1 g 5 g | $78.00 $278.00 | ||
Cis-4-Hydroxy-D-proline is a chiral reagent characterized by its distinctive pyrrolidine ring, which facilitates unique stereoelectronic effects during chemical reactions. The hydroxyl group at the 4-position enhances its ability to engage in intramolecular hydrogen bonding, influencing reaction kinetics and selectivity. This compound's conformational flexibility allows it to adopt various spatial arrangements, optimizing interactions with substrates and promoting enantioselective transformations. | ||||||
D-(+)-3-Phenyllactic acid | 7326-19-4 | sc-252655 | 5 g | $214.00 | ||
D-(+)-3-Phenyllactic acid acts as a chiral reagent, notable for its ability to engage in stereoselective reactions due to its unique chiral center. The presence of the phenyl group enhances its interaction with various substrates, promoting specific molecular alignments that favor the formation of enantiomerically enriched products. Its capacity to participate in esterification and amidation reactions showcases its versatility, influencing reaction pathways and kinetics in asymmetric synthesis. | ||||||
(+)-Usnic acid | 7562-61-0 | sc-251412 | 5 g | $50.00 | ||
(+)-Usnic acid is a versatile chiral reagent known for its unique ability to engage in stereoselective reactions due to its rigid bicyclic structure. This compound exhibits strong hydrogen bonding capabilities, which can stabilize transition states and enhance enantioselectivity. Its distinct molecular conformation allows for selective interactions with various substrates, influencing reaction pathways and kinetics, making it a valuable tool in asymmetric synthesis. | ||||||
(−)-α-Pinene | 7785-26-4 | sc-239166 | 25 g | $43.00 | ||
(-)-α-Pinene is a chiral reagent characterized by its unique bicyclic structure, which facilitates specific molecular interactions in asymmetric synthesis. Its inherent strain and steric hindrance promote selective binding to substrates, enhancing enantioselectivity in reactions. The compound's ability to form transient complexes with reactants can significantly influence reaction kinetics, leading to distinct pathways and improved yields in chiral transformations. | ||||||