(S,S)-DACH-phenyl trost ligand

95%

Reagent Code: #127080
label
Alias (1S,2S)-(-)-1,2-Cyclohexanediamine-N,N'-bis(2-diphenylphosphinobenzoyl); (S,S)-DACH-phenyl
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CAS Number 169689-05-8

science Other reagents with same CAS 169689-05-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 690.75 g/mol
Formula C₄₄H₄₀N₂O₂P₂
badge Registry Numbers
MDL Number MFCD01631274
thermostat Physical Properties
Melting Point 134-136°C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

The (S,S)-DACH-phenyl trost ligand is widely used in asymmetric catalysis, particularly in the synthesis of chiral compounds. It is highly effective in facilitating enantioselective reactions, such as allylic alkylations, which are crucial for producing pharmaceuticals and fine chemicals with high optical purity. This ligand is often employed in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its application extends to the production of agrochemicals and specialty chemicals, where precise control over molecular chirality is essential for efficacy and safety. Additionally, it is utilized in academic and industrial research to explore new catalytic processes and optimize synthetic routes for complex molecules.

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Test Parameter Specification
Appearance White to Tan Solid, Powder,Crystals and/or Chunks
Purity (%) 94.5-100
Specific Rotation ([A]20/D (C=1,MeOH))(deg) -141--127
Infrared spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,239.00
inventory 250mg
10-20 days ฿1,323.00
inventory 5g
10-20 days ฿17,928.00

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(S,S)-DACH-phenyl trost ligand
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The (S,S)-DACH-phenyl trost ligand is widely used in asymmetric catalysis, particularly in the synthesis of chiral compounds. It is highly effective in facilitating enantioselective reactions, such as allylic alkylations, which are crucial for producing pharmaceuticals and fine chemicals with high optical purity. This ligand is often employed in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its application extends to the pr

The (S,S)-DACH-phenyl trost ligand is widely used in asymmetric catalysis, particularly in the synthesis of chiral compounds. It is highly effective in facilitating enantioselective reactions, such as allylic alkylations, which are crucial for producing pharmaceuticals and fine chemicals with high optical purity. This ligand is often employed in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its application extends to the production of agrochemicals and specialty chemicals, where precise control over molecular chirality is essential for efficacy and safety. Additionally, it is utilized in academic and industrial research to explore new catalytic processes and optimize synthetic routes for complex molecules.

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