95322-86-4 Usage
Uses
Used in Pharmaceutical Industry:
(2-methoxyphenyl)phenylphosphinic acid is used as a building block in the synthesis of various organic compounds, such as phosphonate esters and metal complexes. It has potential applications in the development of new pharmaceuticals due to its unique chemical properties.
Used in Agrochemical Industry:
MPPA is also used in the agrochemical industry as a building block for the synthesis of various organic compounds that can be used in the development of new agrochemicals.
Used in Antioxidant Applications:
(2-methoxyphenyl)phenylphosphinic acid has been investigated for its potential as an antioxidant, which can help protect against oxidative stress and damage in various applications.
Used in Catalytic Reactions:
MPPA has also been studied for its potential as a ligand in catalytic reactions, which can improve the efficiency and selectivity of various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 95322-86-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,3,2 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 95322-86:
(7*9)+(6*5)+(5*3)+(4*2)+(3*2)+(2*8)+(1*6)=144
144 % 10 = 4
So 95322-86-4 is a valid CAS Registry Number.
95322-86-4Relevant academic research and scientific papers
Practical synthesis of chiral vinylphosphine oxides by direct nucleophilic substitution. Stereodivergent synthesis of aminophosphine ligands
Oliana, Marco,King, Frank,Horton, Peter N.,Hursthouse,Hii, King Kuok
, p. 2472 - 2479 (2007/10/03)
A practical synthesis of optically pure alkylphenylvinylphosphine oxides is described, utilizing a nucleophilic displacement at phosphorus to install the vinyl moiety. The products were used to prepare classes of P-stereogenic aminophosphine (PN) and aminohydroxyphosphine (PNO) ligands. Stereocontrol can be exerted at various stages of the synthesis, to provide specific combinations of chirality in the final product. The effect of the stereogenic phosphorus and match-mismatch of chiralities of PNO ligands were examined in the asymmetric ruthenium-catalyzed hydrogen transfer reduction of three aryl ketones.
