(1R,2R)-2-N,2-N-dimethylcyclohexane-1,2-diamine

98%

Reagent Code: #229957
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CAS Number 67198-21-4

science Other reagents with same CAS 67198-21-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 142.24 g/mol
Formula C₈H₁₈N₂
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective hydrogenation and transfer hydrogenation reactions. Its rigid cyclohexane backbone and defined stereochemistry make it effective in inducing high enantioselectivity when complexed with transition metals like ruthenium or rhodium. Commonly applied in the synthesis of chiral amines and pharmaceutical intermediates where stereochemical purity is critical. Also employed in organocatalysis and as a building block for more complex chiral catalysts.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿320.00
5g
10-20 days ฿1,300.00
25g
10-20 days ฿6,060.00
100g
10-20 days ฿24,030.00
(1R,2R)-2-N,2-N-dimethylcyclohexane-1,2-diamine
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective hydrogenation and transfer hydrogenation reactions. Its rigid cyclohexane backbone and defined stereochemistry make it effective in inducing high enantioselectivity when complexed with transition metals like ruthenium or rhodium. Commonly applied in the synthesis of chiral amines and pharmaceutical intermediates where stereochemical purity is critical. Also employed in organocatalysis and as a building block for more comple

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective hydrogenation and transfer hydrogenation reactions. Its rigid cyclohexane backbone and defined stereochemistry make it effective in inducing high enantioselectivity when complexed with transition metals like ruthenium or rhodium. Commonly applied in the synthesis of chiral amines and pharmaceutical intermediates where stereochemical purity is critical. Also employed in organocatalysis and as a building block for more complex chiral catalysts.

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