Chiral Reagents
Items 191 to 200 of 465 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
(R)-(+)-1,1′-Bi(2-naphthylamine) | 18741-85-0 | sc-253392 sc-253392A | 250 mg 1 g | $70.00 $125.00 | ||
(R)-(+)-1,1'-Bi(2-naphthylamine) is a chiral reagent notable for its ability to stabilize transition states through π-π stacking interactions and steric hindrance. This compound exhibits unique chiral induction properties, facilitating enantioselective reactions by preferentially stabilizing one enantiomer over the other. Its rigid structure enhances selectivity in catalytic processes, while its solubility in organic solvents allows for efficient reaction kinetics in asymmetric synthesis. | ||||||
(−)-Terpinen-4-ol | 20126-76-5 | sc-229365 | 25 g | $104.00 | ||
(-)-Terpinen-4-ol serves as a chiral reagent characterized by its ability to form hydrogen bonds and engage in dipole-dipole interactions, which influence reaction pathways. Its unique stereochemistry promotes enantioselectivity by preferentially stabilizing specific transition states. The compound's moderate polarity enhances solubility in various solvents, facilitating efficient reaction kinetics and improving the selectivity of asymmetric transformations in synthetic applications. | ||||||
(−)-Dihydrocarveol | 20549-47-7 | sc-227865 | 1 ml | $50.00 | ||
(-)-Dihydrocarveol is a chiral reagent notable for its unique steric configuration, which allows it to selectively interact with substrates through non-covalent interactions such as van der Waals forces and hydrophobic effects. This compound's distinct spatial arrangement can influence the orientation of reactants, leading to enhanced enantioselectivity in asymmetric synthesis. Its moderate polarity and ability to form stable complexes contribute to favorable reaction kinetics, optimizing yields in chiral transformations. | ||||||
α-Solanine | 20562-02-1 | sc-252340 sc-252340A sc-252340B | 5 mg 10 mg 50 mg | $162.00 $237.00 $779.00 | 2 | |
α-Solanine serves as a chiral reagent characterized by its intricate stereochemistry, which facilitates specific interactions with chiral centers in substrates. Its unique molecular framework promotes selective binding through hydrogen bonding and dipole-dipole interactions, enhancing enantioselectivity in various reactions. The compound's ability to stabilize transition states can significantly influence reaction pathways, leading to improved efficiency and selectivity in asymmetric synthesis processes. | ||||||
(+)-cis,trans-Abscisic acid | 21293-29-8 | sc-202103 sc-202103A | 500 µg 1 mg | $107.00 $192.00 | ||
(+)-cis,trans-Abscisic acid is a chiral reagent notable for its ability to modulate molecular interactions through its unique stereochemical configuration. This compound exhibits strong hydrogen bonding capabilities, which can influence the orientation of substrates during reactions. Its distinct conformational flexibility allows for the stabilization of specific transition states, thereby enhancing reaction kinetics and promoting enantioselective outcomes in asymmetric synthesis. | ||||||
Ostreogrycin A | 21411-53-0 | sc-202269 | 5 mg | $422.00 | ||
Ostreogrycin A is a chiral reagent notable for its intricate molecular structure, which enables specific non-covalent interactions with various substrates. Its unique stereochemical configuration allows for selective binding to chiral catalysts, enhancing reaction pathways that favor enantioselective outcomes. The compound exhibits distinct kinetic profiles, with its reactivity modulated by solvent effects and temperature, making it a versatile tool in asymmetric synthesis. | ||||||
(S)-(−)-α-Methylbenzyl isocyanide | 21872-32-2 | sc-229198 | 1 g | $151.00 | ||
(S)-(-)-α-Methylbenzyl isocyanide serves as a chiral reagent characterized by its ability to form strong dipole-dipole interactions due to the isocyanide functional group. This compound's unique steric and electronic properties facilitate selective coordination with metal catalysts, promoting enantioselective transformations. Its reactivity is influenced by steric hindrance and solvent polarity, allowing for tailored reaction conditions in asymmetric synthesis. | ||||||
(S)-Ketoprofen | 22161-81-5 | sc-200624 | 1 g | $118.00 | ||
(S)-Ketoprofen is a chiral reagent notable for its ability to engage in specific hydrogen bonding interactions, enhancing selectivity in asymmetric reactions. Its unique spatial arrangement allows for effective coordination with various catalysts, influencing reaction pathways and kinetics. The compound's distinct conformational flexibility can lead to varied reactivity profiles, making it a versatile tool in chiral synthesis. Additionally, its solubility characteristics can be manipulated to optimize reaction conditions. | ||||||
(+)-Dihydrocarveol | 22567-21-1 | sc-227864 | 5 ml | $164.00 | ||
(+)-Dihydrocarveol serves as a chiral reagent distinguished by its unique stereochemistry, which facilitates selective interactions in catalytic processes. Its ability to form stable complexes with metal catalysts enhances enantioselectivity in various reactions. The compound's hydrophobic regions promote specific molecular interactions, influencing reaction dynamics and rates. Furthermore, its conformational diversity allows for tailored reactivity, making it a valuable asset in asymmetric synthesis. | ||||||
(S,S)-(−)-2-Amino-1,2-diphenylethanol | 23190-17-2 | sc-255529 | 500 mg | $213.00 | ||
(S,S)-(-)-2-Amino-1,2-diphenylethanol is a chiral reagent characterized by its dual aromatic rings, which provide a rigid framework for stereochemical control in asymmetric reactions. Its amino group can engage in hydrogen bonding, enhancing selectivity and influencing reaction pathways. The compound's ability to stabilize transition states through specific interactions leads to improved enantioselectivity, making it a crucial component in the design of chiral catalysts and reagents. | ||||||