Bis(3,5-di-tert-butyl-4-methoxyphenyl)chlorophosphine

90%

Reagent Code: #141166
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CAS Number 212713-08-1

science Other reagents with same CAS 212713-08-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 505.13 g/mol
Formula C₃₀H₄₆ClO₂P
badge Registry Numbers
MDL Number MFCD08458881
thermostat Physical Properties
Melting Point 116-120°C
Boiling Point 552.5°C
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas storage

description Product Description

Used as a ligand precursor in transition metal catalysis, particularly in palladium-catalyzed cross-coupling reactions. Its bulky, electron-rich structure enhances catalyst stability and reactivity, improving yields in C–C and C–heteroatom bond formations. Commonly applied in pharmaceutical synthesis and fine chemical manufacturing where high selectivity and efficiency are required. Also employed in the development of specialized organophosphorus compounds for materials science and ligand design.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance WHITE TO OFF WHITE SOLID
Purity (%) 89.5-100
MELTING POINT (C) 115-120

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿14,500.00
1g
10-20 days ฿49,500.00
Bis(3,5-di-tert-butyl-4-methoxyphenyl)chlorophosphine
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Used as a ligand precursor in transition metal catalysis, particularly in palladium-catalyzed cross-coupling reactions. Its bulky, electron-rich structure enhances catalyst stability and reactivity, improving yields in C–C and C–heteroatom bond formations. Commonly applied in pharmaceutical synthesis and fine chemical manufacturing where high selectivity and efficiency are required. Also employed in the development of specialized organophosphorus compounds for materials science and ligand design.

Used as a ligand precursor in transition metal catalysis, particularly in palladium-catalyzed cross-coupling reactions. Its bulky, electron-rich structure enhances catalyst stability and reactivity, improving yields in C–C and C–heteroatom bond formations. Commonly applied in pharmaceutical synthesis and fine chemical manufacturing where high selectivity and efficiency are required. Also employed in the development of specialized organophosphorus compounds for materials science and ligand design.

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