Rel-(2R,3S)-2,3-Bis(4-Chlorophenyl)-2,3-Butanediamine

98%

Reagent Code: #231525
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CAS Number 939983-16-1

science Other reagents with same CAS 939983-16-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 309.23 g/mol
Formula C₁₆H₁₈Cl₂N₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral ligand in asymmetric synthesis, particularly in catalytic hydrogenation reactions. Its stereochemistry enables high enantioselectivity, making it valuable in the pharmaceutical industry for producing single-enantiomer drugs. Commonly employed in transition metal complexes with ruthenium or rhodium to enhance catalytic efficiency. Also applied in the development of chiral catalysts for carbon-carbon bond-forming reactions, supporting the synthesis of complex organic molecules with precise stereocontrol.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿11,140.00
250mg
10-20 days ฿18,560.00
1g
10-20 days ฿36,040.00
Rel-(2R,3S)-2,3-Bis(4-Chlorophenyl)-2,3-Butanediamine
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Used as a chiral ligand in asymmetric synthesis, particularly in catalytic hydrogenation reactions. Its stereochemistry enables high enantioselectivity, making it valuable in the pharmaceutical industry for producing single-enantiomer drugs. Commonly employed in transition metal complexes with ruthenium or rhodium to enhance catalytic efficiency. Also applied in the development of chiral catalysts for carbon-carbon bond-forming reactions, supporting the synthesis of complex organic molecules with precise

Used as a chiral ligand in asymmetric synthesis, particularly in catalytic hydrogenation reactions. Its stereochemistry enables high enantioselectivity, making it valuable in the pharmaceutical industry for producing single-enantiomer drugs. Commonly employed in transition metal complexes with ruthenium or rhodium to enhance catalytic efficiency. Also applied in the development of chiral catalysts for carbon-carbon bond-forming reactions, supporting the synthesis of complex organic molecules with precise stereocontrol.

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