Chiral Reagents
Items 171 to 180 of 466 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Tranexamic acid | 1197-18-8 | sc-204921 sc-204921A | 5 g 10 g | $28.00 $49.00 | 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. | ||||||
(-)-(1S,2S,5S)-2-Hydroxy-3-pinanone | 1845-25-6 | sc-208900 | 5 g | $167.00 | ||
(-)-(1S,2S,5S)-2-Hydroxy-3-pinanone serves as a versatile chiral reagent, characterized by its unique bicyclic structure that promotes selective interactions in asymmetric synthesis. The compound's hydroxyl group enhances hydrogen bonding capabilities, influencing reaction kinetics and facilitating the formation of stable intermediates. Its distinct steric environment allows for tailored reactivity, making it an effective tool for achieving high enantioselectivity in various synthetic pathways. | ||||||
(+)-Neomenthol | 2216-52-6 | sc-237841 | 5 g | $130.00 | ||
(+)-Neomenthol is a chiral reagent distinguished by its unique bicyclic framework, which imparts significant steric hindrance and influences molecular interactions during asymmetric synthesis. The compound's tertiary alcohol group enhances its ability to form hydrogen bonds, promoting specific reaction pathways and stabilizing transition states. This structural arrangement allows for precise control over enantioselectivity, making it a valuable asset in the development of chiral compounds. | ||||||
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. | ||||||
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. | ||||||
(S)-(+)-1,2-Propanediol | 4254-15-3 | sc-236755 | 5 g | $157.00 | ||
(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. | ||||||
Carbenicillin solution | sc-278810 | 1 ml | $428.00 | |||
Carbenicillin solution acts as a chiral reagent, exhibiting distinctive interactions through its carboxyl and amide functionalities. These groups enable the formation of stable complexes with metal ions, influencing catalytic pathways. Its unique stereochemical configuration allows for selective binding to chiral catalysts, enhancing enantioselectivity. Additionally, the compound's solubility characteristics and reactivity with electrophiles contribute to its role in facilitating asymmetric synthesis, optimizing reaction kinetics. | ||||||
D,L-Alanosine Sodium Salt | 5854-95-5 free acid | sc-207489 sc-207489A | 25 mg 250 mg | $296.00 $1836.00 | ||
D,L-Alanosine Sodium Salt serves as a chiral reagent, characterized by its ability to engage in specific hydrogen bonding interactions due to its amino and hydroxyl groups. This facilitates the formation of chiral environments that can influence reaction pathways. Its unique stereochemistry promotes selective interactions with substrates, enhancing enantioselectivity in various reactions. Furthermore, its solubility in polar solvents aids in optimizing reaction conditions, improving overall efficiency in asymmetric synthesis. | ||||||
Cholesteryl chloroformate | 7144-08-3 | sc-239543 | 25 g | $54.00 | ||
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. | ||||||