5068-20-2

Basic information

• Product Name: (4-(hydroxyMethyl)phenyl)diphenylphosphine oxide
• Synonyms: (4-(hydroxyMethyl)phenyl)diphenylphosphine oxide
• CAS NO: 5068-20-2
• Molecular Weight: 308.317
• Mol File: 5068-20-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (4-(hydroxyMethyl)phenyl)diphenylphosphine oxide(CAS DataBase Reference)
• NIST Chemistry Reference: (4-(hydroxyMethyl)phenyl)diphenylphosphine oxide(5068-20-2)
• EPA Substance Registry System: (4-(hydroxyMethyl)phenyl)diphenylphosphine oxide(5068-20-2)

Safety Data

• Hazardous Substances Data: 5068-20-2(Hazardous Substances Data)

Usage

General Description

(4-(hydroxyMethyl)phenyl)diphenylphosphine oxide is a chemical compound with the molecular formula C19H17O2P. It is an organophosphorus compound that is commonly used as a photoinitiator in the production of polymers and plastics, as well as in UV-cured inks and coatings. Its role as a photoinitiator means that it can initiate or accelerate the polymerization process when exposed to ultraviolet light, making it an important component in the manufacturing of various plastic and polymer products. Additionally, it has also been studied for potential pharmaceutical applications and as a dye for bioimaging due to its fluorescence properties. However, it is important to handle and use this chemical with caution, as it is a known skin and eye irritant and may pose other health hazards if not properly managed.

Upstream product

• 2272-04-0 diphenyl[(4-carboxy)phenyl]phosphine oxide 
• 101630-35-7 (4-(ethoxycarbonyl)phenyl)diphenylphosphine oxide 
• 1031-93-2 diphenyl(p-tolyl)phosphine 
• 873-75-6 4-bromobenzenemethanol 
• 6840-28-4 diphenyl(p-tolyl)phosphine oxide 
• 59016-93-2 p-hydroxymethylphenylboronic acid 
• 4559-70-0 Diphenylphosphine oxide 

Relevant articles and documents

SYNTHESIS STRATEGY FOR GAP PROTECTING GROUP

The present invention relates to a novel synthesis method to form particular molecules. These molecules have multiple uses, most notably in the field of protecting groups used throughout organic and synthetic chemistry. The disclosed method is safer, more

SYSTEM AND METHOD FOR SOLUTION PHASE GAP PEPTIDE SYNTHESIS

Disclosed is a system and method for Fmoc/tBu solution-phase peptide synthesis including the development of a new benzyl-type GAP protecting group, and related uses thereto. This novel GAP protecting group is utilized in place of a polymer support, facilitating C to N Fmoc peptide synthesis without chromatography, recrystallization, or polymer supports. The GAP group can be added and removed in high yield.

Palladium-catalyzed air-based oxidative coupling of arylboronic acids with H-phosphine oxides leading to aryl phosphine oxides

We present a novel and highly efficient methodology that allows for the construction of C-P bonds via the palladium-catalyzed air-based oxidative coupling of various commercially available arylboronic acids with easily oxidized H-phosphine oxides leading to valuable aryl phosphine oxides, particularly triarylphosphine oxides, with the use of air as the green oxidant, broad substrate applicability and good to excellent yields. The described catalytic system should be an efficient complement to the Chan-Lam type reaction and be useful in synthetic programs. This journal is the Partner Organisations 2014.