795-44-8

Basic information

• Product Name: 4-Methoxyphenyldiphenylphosphine oxide
• Synonyms: (4-Methoxyphenyl)diphenylphosphine oxide;(p-Anisyl)diphenylphosphine oxide;1-(Diphenylphosphinyl)-4-methoxybenzene;4-Methoxyphenyldiphenylphosphine oxide
• CAS NO: 795-44-8
• Molecular Formula: C₁₉H₁₇O₂P
• Molecular Weight: 308.310841
• Mol File: 795-44-8.mol
• Article Data: 46

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-Methoxyphenyldiphenylphosphine oxide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Methoxyphenyldiphenylphosphine oxide(795-44-8)
• EPA Substance Registry System: 4-Methoxyphenyldiphenylphosphine oxide(795-44-8)

Safety Data

• Hazardous Substances Data: 795-44-8(Hazardous Substances Data)

Usage

Description

4-Methoxyphenyldiphenylphosphine oxide is a chemical compound with the molecular formula C19H17O2P. It is a versatile photoinitiator used in the production of polymers, plastics, UV-curable coatings, and inks.

Uses

Used in Adhesives Industry:
4-Methoxyphenyldiphenylphosphine oxide is used as a photoinitiator for [application reason] in the adhesives industry. It helps in the rapid curing of adhesives under UV light, improving their adhesion and mechanical properties.
Used in Electronics Industry:
4-Methoxyphenyldiphenylphosphine oxide is used as a photoinitiator for [application reason] in the electronics industry. It enables the fast curing of polymers and plastics used in electronic components, enhancing their performance and durability.
Used in Medical Devices Industry:
4-Methoxyphenyldiphenylphosphine oxide is used as a photoinitiator for [application reason] in the medical devices industry. It aids in the production of high-performance polymers and plastics used in medical devices, ensuring their safety and reliability.
Used in Coatings and Inks Industry:
4-Methoxyphenyldiphenylphosphine oxide is used as a photoinitiator for [application reason] in the coatings and inks industry. It facilitates the quick curing of UV-curable coatings and inks, resulting in improved adhesion, durability, and performance.

Upstream product

• 104-92-7 1-bromo-4-methoxy-benzene 
• 2959-74-2 benzyldiphenylphosphine oxide 
• 696-62-8 para-iodoanisole 
• 34676-89-6 diphenylphosphide ion 
• 55743-31-2 (1-chlorovinyl)diphenylphosphine oxide 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 3878-45-3 triphenylphosphine sulfide 
• 791-28-6 Triphenylphosphine oxide 
• 66107-29-7 4-methoxyphenyl triflate 
• 829-85-6 diphenylphosphane 
• 4455-77-0 (methoxymethyl)diphenylphosphine oxide 
• 1079-66-9 chloro-diphenylphosphine 
• 459-64-3 4-methoxybenzenediazonium tetrafluoroborate 
• 4559-70-0 Diphenylphosphine oxide 

Downstream Products

• 793-43-1 (4-Hydroxyphenyl)diphenylphosphine oxide 
• 896-89-9 (4-methoxyphenyl)diphenylphosphane 
• 14180-49-5 (4-methoxyphenyl)diphenylphosphine sulfide 
• 20650-56-0 p-hydroxyphenyl(diphenyl)phosphine sulfide 
• 394657-29-5 p-hydroxyphenyl(diphenyl)phosphine selenide 
• 528609-62-3 (4-hydroxyphenyl)diphenylphosphine borane 
• 5068-21-3 4-(diphenylphosphanyl)phenol 

Relevant articles and documents

Palladium anchored on a covalent organic framework as a heterogeneous catalyst for phosphorylation of aryl bromides

A simple azine-linked covalent organic framework (COF) with high thermal and chemical stabilities has been prepared by using deep eutectic solvent (DES) as green media. The as-synthesized COF was employed as heterogeneous ligand for immobilization of PdII. The obtained Pd-supported COF nanoparticles catalyst (defined as Pd/TFPT-Azine-COF) was found to be an efficient heterogeneous catalyst for the Hirao reaction of aryl halides and dialkyl phosphites or diphenylphosphine oxide with excellent recyclability, reusability, and retention of crystallinity.

Visible-Light-Induced Nickel-Catalyzed P(O)-C(sp2) Coupling Using Thioxanthen-9-one as a Photoredox Catalysis

An efficient method has been developed for photocatalytic P(O)-C(sp2) coupling of (hetero)aryl halides with H-phosphine oxides or H-phosphites under the irradiation of visible light or sunlight. The thioxanthen-9-one/nickel dual catalysis mediates this ph

NiCl 2as a Cheap and Efficient Precatalyst for the Coupling of Aryl Fluorosulfonate and Phosphite/Phosphine Oxide

Herein, NiCl 2is employed as a cheap precatalyst in the formation of C(sp 2)-P bond via cross-coupling reaction of phenol derivatives and phosphine oxides/phosphites. This catalytic system allows a variety of phenols with diverse functional groups to transform into phosphates with good yields. No additional additive is used in this reaction.