Diphenyl-2-pyridylphosphine

97%

Reagent Code: #68924
label
Alias Diphenyl-2-pyridylphosphine ; 2-pyridyldiphenylphosphine
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CAS Number 37943-90-1

science Other reagents with same CAS 37943-90-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 263.27 g/mol
Formula C₁₇H₁₄NP
badge Registry Numbers
MDL Number MFCD00192108
thermostat Physical Properties
Melting Point 82-84 °C (dec.)(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used as a ligand in transition metal catalysis, particularly in cross-coupling reactions like Suzuki-Miyaura and Heck reactions, enhancing reaction efficiency and selectivity.

Applied in the synthesis of organic compounds, including pharmaceuticals and agrochemicals, due to its ability to stabilize metal complexes and facilitate complex transformations.

Employed in the development of advanced materials, such as polymers and coordination polymers, where its phosphine group acts as a key building block.

Also utilized in asymmetric synthesis, enabling the production of chiral molecules with high enantiomeric purity, which is crucial in drug development.

Its role in photochemical and electrochemical processes makes it valuable in research on energy storage and conversion technologies.

format_list_bulleted Product Specification

Test Parameter Specification
Elemental Analysis 74.85-80.27
Melting point 81-85
Purity 97-100
Appearance White crystalline powder
Infrared Spectrum Conforms to Structure
Solubility in Toluene almost transparent

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿500.00
inventory 100g
10-20 days ฿5,580.00
inventory 25g
10-20 days ฿1,590.00

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Diphenyl-2-pyridylphosphine
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Used as a ligand in transition metal catalysis, particularly in cross-coupling reactions like Suzuki-Miyaura and Heck reactions, enhancing reaction efficiency and selectivity.

Applied in the synthesis of organic compounds, including pharmaceuticals and agrochemicals, due to its ability to stabilize metal complexes and facilitate complex transformations.

Employed in the development of advanced materials, such as polymers and coordination polymers, where its phosphine group acts as a key buildi

Used as a ligand in transition metal catalysis, particularly in cross-coupling reactions like Suzuki-Miyaura and Heck reactions, enhancing reaction efficiency and selectivity.

Applied in the synthesis of organic compounds, including pharmaceuticals and agrochemicals, due to its ability to stabilize metal complexes and facilitate complex transformations.

Employed in the development of advanced materials, such as polymers and coordination polymers, where its phosphine group acts as a key building block.

Also utilized in asymmetric synthesis, enabling the production of chiral molecules with high enantiomeric purity, which is crucial in drug development.

Its role in photochemical and electrochemical processes makes it valuable in research on energy storage and conversion technologies.

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