884-74-2 Usage
Description
(DIPHENYLPHOSPHORYL)METHANOL, also known as DPPM, is a chemical compound with the formula (C6H5)2P(O)CH2OH. It is an organophosphorus compound that is widely used as a ligand in coordination chemistry and as a precursor in organic synthesis. DPPM is a white crystalline solid that is soluble in organic solvents and has a melting point of 112-114°C. It is commonly utilized as a catalyst in various chemical reactions such as hydroformylation, hydrogenation, and metal complexation. DPPM is also known for its potential applications in pharmaceuticals, agrochemicals, and materials science, making it a valuable and versatile compound in the field of chemistry.
Uses
Used in Coordination Chemistry:
(DIPHENYLPHOSPHORYL)METHANOL is used as a ligand for [forming metal complexes] for [enhancing the stability and reactivity of metal centers in various chemical reactions].
Used in Organic Synthesis:
(DIPHENYLPHOSPHORYL)METHANOL is used as a precursor for [synthesis of various organic compounds] for [creating a wide range of molecules with diverse applications].
Used in Pharmaceutical Industry:
(DIPHENYLPHOSPHORYL)METHANOL is used as a catalyst for [facilitating specific pharmaceutical reactions] for [improving the efficiency and selectivity of drug synthesis].
Used in Agrochemical Industry:
(DIPHENYLPHOSPHORYL)METHANOL is used as a catalyst for [optimizing agrochemical production processes] for [enhancing the yield and quality of agrochemical products].
Used in Materials Science:
(DIPHENYLPHOSPHORYL)METHANOL is used as a component for [developing new materials with specific properties] for [advancing the field of materials science and technology].
Check Digit Verification of cas no
The CAS Registry Mumber 884-74-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,8 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 884-74:
(5*8)+(4*8)+(3*4)+(2*7)+(1*4)=102
102 % 10 = 2
So 884-74-2 is a valid CAS Registry Number.
884-74-2Relevant articles and documents
Cyclooctene epoxidation with H2O2 and single crystal X-ray determined crystal structures of new molybdenum and tungsten catalysts bearing the hydrophilic ligand hydroxymethyldiphenylphosphine oxide
Feng, Linsheng,Urnezius, Eugenijus,Luck, Rudy L.
, p. 1564 - 1571 (2008)
The dioxo molybdenum and tungsten complexes MoO2Cl2(OPPh2CH2OH)2 and WO2Cl2(OPPh2CH2OH)2 have been synthesized and characterized by FT-IR, 1
C-Alkyl-bis-phosphoryl chelating systems for the potential recovery of strategic metals
Babouri, Rachida,Halidou Dougourikoye, Abdoul Razak,Ilagouma, Amadou TidJani,Pirat, Jean-Luc,Virieux, David,Volle, Jean-No?l
, (2020/09/07)
Methylene-bis-phosphonic acid and derivatives are used as complexing agents, diagnostics, therapeutics and show interesting virustatic properties. We describe the syntheses of mono- and di-substituted bisphosphonates and mono- and disubstituted diethyl ((diphenylphosphoryl)methyl)phosphonate as possible chelating systems for the recovery of strategic metals.
Reduction of Tertiary Phosphine Oxides by BH 3 Assisted by Neighboring Activating Groups
Sowa, Sylwia,Stankevi?, Marek,Flis, Anna,Pietrusiewicz, K. Micha?
, p. 2106 - 2118 (2018/02/28)
Tertiary sulfanylphosphine and aminoalkylphosphine oxides can be easily converted into the corresponding tertiary sulfanylphosphine- and aminoalkylphosphine-boranes, respectively, through the facile P=O bond reduction by borane complexes. The easy reduction of the strong P=O bond by BH 3, a mild reducing agent, has been achieved through an intramolecular P=O - B complexation directed by proximal SH or NH activating groups located at the α- or β-position to the P=O bond. A generalized reduction mechanism has been proposed.
