N,N'-((1R,2R)-cyclohexane-1,2-diyl)dimethanesulfonamide

95%

Reagent Code: #217355
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CAS Number 122833-58-3

science Other reagents with same CAS 122833-58-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 270.37 g/mol
Formula C₈H₁₈N₂O₄S₂
thermostat Physical Properties
Melting Point 156-157°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a chiral derivatizing agent in asymmetric synthesis, particularly in the resolution of racemic mixtures. Its rigid cyclohexane backbone with defined stereochemistry allows it to act as a chiral auxiliary or selector in enantioselective reactions. Commonly employed in pharmaceutical intermediates synthesis where stereochemical control is critical. Also utilized in coordination chemistry as a ligand for chiral metal complexes, facilitating catalytic asymmetric transformations such as alkylations and epoxidations. Shows utility in analytical chemistry for chiral HPLC stationary phases due to its ability to differentiate enantiomers.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿900.00
inventory 100mg
10-20 days ฿2,330.00
inventory 250mg
10-20 days ฿2,830.00
inventory 1g
10-20 days ฿10,820.00
inventory 5g
10-20 days ฿44,580.00
inventory 25g
10-20 days ฿174,420.00

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N,N'-((1R,2R)-cyclohexane-1,2-diyl)dimethanesulfonamide
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Used as a chiral derivatizing agent in asymmetric synthesis, particularly in the resolution of racemic mixtures. Its rigid cyclohexane backbone with defined stereochemistry allows it to act as a chiral auxiliary or selector in enantioselective reactions. Commonly employed in pharmaceutical intermediates synthesis where stereochemical control is critical. Also utilized in coordination chemistry as a ligand for chiral metal complexes, facilitating catalytic asymmetric transformations such as alkylations an

Used as a chiral derivatizing agent in asymmetric synthesis, particularly in the resolution of racemic mixtures. Its rigid cyclohexane backbone with defined stereochemistry allows it to act as a chiral auxiliary or selector in enantioselective reactions. Commonly employed in pharmaceutical intermediates synthesis where stereochemical control is critical. Also utilized in coordination chemistry as a ligand for chiral metal complexes, facilitating catalytic asymmetric transformations such as alkylations and epoxidations. Shows utility in analytical chemistry for chiral HPLC stationary phases due to its ability to differentiate enantiomers.

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