(S)-(-)-2,2'-Bis(di-p-tolylphosphino)-1,1'-binaphthyl

98%

Reagent Code: #68690
label
Alias (S)-(-)-2,2-Bis(xylylphosphine)-1,1-binaphthalene
fingerprint
CAS Number 100165-88-6

science Other reagents with same CAS 100165-88-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 678.78 g/mol
Formula C₄₈H₄₀P₂
badge Registry Numbers
MDL Number MFCD01311709
thermostat Physical Properties
Melting Point 252-256 °C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective hydrogenation, carbon-carbon bond formation, and other transformations where high stereochemical control is required. Its application is prominent in the pharmaceutical industry for the synthesis of chiral drugs and intermediates, ensuring the production of single enantiomers with high purity. Additionally, it is utilized in academic research to develop new catalytic methodologies and explore novel asymmetric reactions. Its robust structure and high selectivity make it a valuable tool in organic synthesis.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White powder
Melting Point 252-259
Purity 98
A20 Dc 1.052 benzene -167 to -157

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿640.00
inventory 1g
10-20 days ฿1,860.00
inventory 5g
10-20 days ฿7,960.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-(-)-2,2'-Bis(di-p-tolylphosphino)-1,1'-binaphthyl
No image available
This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective hydrogenation, carbon-carbon bond formation, and other transformations where high stereochemical control is required. Its application is prominent in the pharmaceutical industry for the synthesis of chiral drugs and intermediates, ensuring the production of single enantiomers with high purity. Additionally, it is utilized in academic research to develop new catalytic methodologies and explore novel asymmetric reactions. Its robust structure and high selectivity make it a valuable tool in organic synthesis.
Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...