2-[Bis(3,5-dimethylphenyl)phosphino]benzaldehyde

98%

Reagent Code: #68772
fingerprint
CAS Number 669091-00-3

science Other reagents with same CAS 669091-00-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 346.4 g/mol
Formula C₂₃H₂₃OP
badge Registry Numbers
MDL Number MFCD15143662
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

description Product Description

This chemical is primarily utilized as a ligand in catalytic processes, particularly in transition metal-catalyzed reactions. Its structure, featuring a phosphine group and an aldehyde moiety, makes it effective in facilitating cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, which are crucial in organic synthesis for creating complex molecules. Additionally, it is employed in asymmetric catalysis, where it helps in producing chiral compounds with high enantioselectivity, important in pharmaceuticals and fine chemicals. Its stability and electronic properties also make it suitable for use in coordination chemistry and material science research.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to Yellow to Tan Solid or Powder
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,990.00
inventory 250mg
10-20 days ฿12,500.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-[Bis(3,5-dimethylphenyl)phosphino]benzaldehyde
No image available

This chemical is primarily utilized as a ligand in catalytic processes, particularly in transition metal-catalyzed reactions. Its structure, featuring a phosphine group and an aldehyde moiety, makes it effective in facilitating cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, which are crucial in organic synthesis for creating complex molecules. Additionally, it is employed in asymmetric catalysis, where it helps in producing chiral compounds with high enantioselectivity, important in

This chemical is primarily utilized as a ligand in catalytic processes, particularly in transition metal-catalyzed reactions. Its structure, featuring a phosphine group and an aldehyde moiety, makes it effective in facilitating cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, which are crucial in organic synthesis for creating complex molecules. Additionally, it is employed in asymmetric catalysis, where it helps in producing chiral compounds with high enantioselectivity, important in pharmaceuticals and fine chemicals. Its stability and electronic properties also make it suitable for use in coordination chemistry and material science research.

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...