Chiral Reagents
Items 111 to 120 of 465 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
(+)-1,2-Bis[(2S,5S)-2,5-dimethylphospholano]benzene | 136735-95-0 | sc-237667 | 100 mg | $68.00 | ||
(+)-1,2-Bis[(2S,5S)-2,5-dimethylphospholano]benzene acts as a chiral reagent by leveraging its unique phospholane framework, which fosters specific steric and electronic interactions. The dual phospholane units create a chiral pocket that effectively stabilizes reactive intermediates, enhancing enantioselectivity in catalytic processes. Its rigid structure promotes distinct reaction pathways, allowing for precise control over stereochemical outcomes in asymmetric synthesis. | ||||||
Docetaxel Metabolites M1 and M3(Mixture of Diastereomers) | sc-218256 | 1 mg | $1080.00 | |||
Docetaxel Metabolites M1 and M3 (Mixture of Diastereomers) serve as chiral reagents through their intricate stereochemical configurations, which facilitate selective molecular interactions. The presence of multiple chiral centers allows for unique binding affinities with substrates, influencing reaction kinetics and promoting enantioselective transformations. Their distinct diastereomeric forms can lead to varied reactivity profiles, enabling tailored approaches in asymmetric synthesis and enhancing the precision of stereochemical control. | ||||||
[(R,R)-1,5-Diaza-cis-decalin]copper hydroxide iodide | sc-301650 | 500 mg | $186.00 | |||
[(R,R)-1,5-Diaza-cis-decalin]copper hydroxide iodide acts as a chiral reagent by leveraging its unique structural framework, which promotes specific interactions with substrates. The copper center enhances coordination with chiral ligands, facilitating distinct reaction pathways. Its ability to stabilize transition states through non-covalent interactions leads to improved enantioselectivity. This compound's distinctive geometry and electronic properties contribute to its effectiveness in asymmetric synthesis, allowing for precise control over stereochemical outcomes. | ||||||
(−)-trans-Caryophyllene | 87-44-5 | sc-251281 sc-251281A sc-251281B sc-251281C | 1 ml 5 ml 25 ml 1 L | $79.00 $157.00 $437.00 $2861.00 | 1 | |
(-)-trans-Caryophyllene serves as a chiral reagent by exhibiting a unique bicyclic structure that influences molecular interactions during reactions. Its rigid framework allows for selective binding with substrates, promoting specific stereochemical pathways. The compound's non-planar conformation enhances steric effects, which can significantly alter reaction kinetics. Additionally, its hydrophobic characteristics facilitate unique solvation dynamics, further optimizing enantioselectivity in asymmetric transformations. | ||||||
(−)-Isopulegol | 89-79-2 | sc-250202 | 1 ml | $86.00 | ||
(-)-Isopulegol acts as a chiral reagent characterized by its flexible cyclohexene ring, which allows for dynamic conformational changes during reactions. This adaptability enhances its ability to engage in specific molecular interactions, promoting unique stereochemical outcomes. The compound's polar functional groups contribute to its solubility properties, facilitating effective substrate interactions. Its distinct spatial arrangement also influences reaction rates, optimizing enantioselectivity in various asymmetric synthesis processes. | ||||||
Isoborneol | 124-76-5 | sc-235391 | 25 g | $27.00 | ||
Isoborneol serves as a chiral reagent, notable for its bicyclic structure that introduces steric hindrance, influencing reaction pathways and selectivity. Its unique arrangement of functional groups enhances intermolecular interactions, allowing for precise control over stereochemical outcomes. The compound's ability to stabilize transition states through non-covalent interactions can significantly affect reaction kinetics, making it a valuable tool in asymmetric synthesis. | ||||||
N-Butylscopolammonium Bromide | 149-64-4 | sc-212165 sc-212165A | 10 mg 500 mg | $135.00 $180.00 | ||
N-Butylscopolammonium Bromide acts as a chiral reagent, characterized by its quaternary ammonium structure that facilitates specific ion-pairing interactions. This compound exhibits unique solvation properties, enhancing its ability to influence reaction mechanisms and selectivity in asymmetric synthesis. Its sterically demanding nature can modulate the reactivity of substrates, while its ionic character promotes distinct pathways, ultimately affecting the stereochemical distribution of products. | ||||||
Vindoline | 2182-14-1 | sc-204940 sc-204940A | 100 mg 1 g | $240.00 $300.00 | ||
Vindoline serves as a chiral reagent, distinguished by its complex indole structure that enables selective interactions with various substrates. Its unique stereochemistry allows for the formation of stable chiral environments, influencing reaction pathways and enhancing enantioselectivity. The compound's ability to engage in hydrogen bonding and π-π stacking interactions further modulates reaction kinetics, promoting specific product formation while minimizing undesired byproducts. | ||||||
2-Methylisoborneol solution | 2371-42-8 | sc-251786 | 1 ml | $320.00 | ||
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. | ||||||
DL-erythro-Dihydrosphingosine | 3102-56-5 | sc-203018 sc-203018A | 10 mg 100 mg | $158.00 $1025.00 | ||
DL-erythro-Dihydrosphingosine serves as a chiral reagent, distinguished by its long-chain aliphatic structure that promotes selective interactions with various substrates. Its unique stereochemistry enhances enantioselectivity, allowing for precise control over reaction outcomes. The compound's amphiphilic characteristics influence its solubility and reactivity, while its capacity for hydrogen bonding and dipole-dipole interactions significantly impacts reaction kinetics and product formation. | ||||||