100065-14-3

Basic information

• Product Name: (2-hydroxy-2-phenylethyl)diphenylphosphine oxide
• Synonyms: (2-hydroxy-2-phenylethyl)diphenylphosphine oxide
• CAS NO: 100065-14-3
• Molecular Weight: 322.343
• Mol File: 100065-14-3.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: (2-hydroxy-2-phenylethyl)diphenylphosphine oxide(CAS DataBase Reference)
• NIST Chemistry Reference: (2-hydroxy-2-phenylethyl)diphenylphosphine oxide(100065-14-3)
• EPA Substance Registry System: (2-hydroxy-2-phenylethyl)diphenylphosphine oxide(100065-14-3)

Safety Data

• Hazardous Substances Data: 100065-14-3(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 101315-74-6 C₂₂H₃₃O₄PTi 
• 101315-76-8 C₂₆H₂₄ClCrO₂P₂ 
• 101248-14-0 C₂₅H₄₀O₅PTi^(1-)*Li⁽¹⁺⁾ 
• 119554-76-6 C₂₆H₂₄NOP 
• 57901-20-9 N-phenyl methyldiphenyl-λ⁵-phosphazene 
• 96-09-3 styrene oxide 
• 829-85-6 diphenylphosphane 
• 100-42-5 styrene 
• 4559-70-0 Diphenylphosphine oxide 
• 133589-20-5 trans-1-phenyl-2-(tributylstannyl)epoxyethane 
• 65567-06-8 lithium diphenylphosphide 
• 2129-89-7 diphenyl(methyl)phosphine oxide 

Downstream Products

• 78045-10-0 (Z)-(2-phenylethenyl)diphenylphosphine oxide 
• 203574-98-5 (1'R)-N-Benzyl-N-(1'-phenylethyl)-2-diphenylphosphinoyl-1-phenylethylamine 
• 372166-93-3 (E)-2-diphenylphosphinyl-2-trimethylsilylstyrene 
• 795-47-1 (E)-diphenyl(styryl)phosphine oxide 
• 117924-18-2 [2-(Diphenyl-phosphinoyl)-1-phenyl-ethoxy]-trimethyl-silane 

Relevant articles and documents

Conformational Analysis of 2-Substituted Alkylphosphoryl Compounds. 4. Substituent Effect on the Nature of the Hydrogen Bonding in (2-Hydroxyalkyl)phosphoryl Systems

The extent to which solid state conformational and hydrogen bonding preferences of five (2-hydroxyalkyl)phosphoryl compounds 2a-e [R12P(O)CH2CH(OH)R2; 2a, R1 = MeO, R2 = Ph; 2b, R1/su

Copper-catalyzed direct hydroxyphosphorylation of electron-deficient alkenes with H-phosphine oxides and dioxygen

A copper-catalyzed direct hydroxyphosphorylation of electron-deficient alkenes with H-phosphine oxides and dioxygen is reported. The present reaction, proceeds under mild reaction conditions with good functional group tolerance, affording the facile and efficient synthesis of various β-hydroxyphosphine oxides in a scaled-up manner with moderate to good yields.

Cobalt(II)-Catalyzed Bisfunctionalization of Alkenes with Diarylphosphine Oxide and Peroxide

The low-cost cobalt(II) catalyst has been used for the first time to achieve P(O)-radical-mediated bisfunctionalization of alkenes with diarylphosphine oxide and peroxides. This simple process is performed under mild conditions to afford a wide variety of phosphonation-peroxidation products in a one-pot manner. Computational studies are carried out to provide a theoretical support for the P(O)-radical-involved bisfunctionalization of alkenes. (Figure presented.).