Bis(3,5-dimethylphenyl)phosphine

98%

Reagent Code: #68937
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CAS Number 71360-06-0

science Other reagents with same CAS 71360-06-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.3 g/mol
Formula C₁₆H₁₉P
badge Registry Numbers
MDL Number MFCD01074629
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Bis(3,5-dimethylphenyl)phosphine is widely used as a ligand in coordination chemistry and catalysis. It plays a crucial role in the development of transition metal complexes, particularly in palladium-catalyzed cross-coupling reactions such as Suzuki, Heck, and Sonogashira reactions. These reactions are essential in the synthesis of pharmaceuticals, agrochemicals, and organic materials. The steric and electronic properties of this ligand enhance the stability and reactivity of the metal centers, improving catalytic efficiency. Additionally, it is employed in the preparation of organometallic compounds for use in material science and polymer chemistry. Its applications also extend to research in asymmetric synthesis, where it aids in creating chiral environments for enantioselective transformations.

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Test Parameter Specification
Appearance Colorless to Tan Liquid
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 10g
10-20 days ฿81,000.00

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Bis(3,5-dimethylphenyl)phosphine
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Bis(3,5-dimethylphenyl)phosphine is widely used as a ligand in coordination chemistry and catalysis. It plays a crucial role in the development of transition metal complexes, particularly in palladium-catalyzed cross-coupling reactions such as Suzuki, Heck, and Sonogashira reactions. These reactions are essential in the synthesis of pharmaceuticals, agrochemicals, and organic materials. The steric and electronic properties of this ligand enhance the stability and reactivity of the metal centers, improvin

Bis(3,5-dimethylphenyl)phosphine is widely used as a ligand in coordination chemistry and catalysis. It plays a crucial role in the development of transition metal complexes, particularly in palladium-catalyzed cross-coupling reactions such as Suzuki, Heck, and Sonogashira reactions. These reactions are essential in the synthesis of pharmaceuticals, agrochemicals, and organic materials. The steric and electronic properties of this ligand enhance the stability and reactivity of the metal centers, improving catalytic efficiency. Additionally, it is employed in the preparation of organometallic compounds for use in material science and polymer chemistry. Its applications also extend to research in asymmetric synthesis, where it aids in creating chiral environments for enantioselective transformations.

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