5435-78-9 Usage
Uses
Used in Pharmaceutical Industry:
(4-nitrophenyl)phenylphosphinic acid is used as a reagent for the production of pharmaceuticals, as it aids in the synthesis of various compounds.
Used in Agrochemical Industry:
(4-nitrophenyl)phenylphosphinic acid is used as a reagent for the production of agrochemicals, contributing to the synthesis of different compounds.
Used as a Corrosion Inhibitor:
(4-nitrophenyl)phenylphosphinic acid is used as a corrosion inhibitor, helping to prevent the degradation of materials in various applications.
Used as a Stabilizer in Polymers:
(4-nitrophenyl)phenylphosphinic acid is used as a stabilizer in polymers, enhancing their durability and performance.
Used as a Precursor in the Synthesis of Phosphorus-containing Compounds:
(4-nitrophenyl)phenylphosphinic acid is used as a precursor in the synthesis of phosphorus-containing compounds, enabling the creation of a variety of molecules.
Used in Catalysis:
(4-nitrophenyl)phenylphosphinic acid is used in catalysis, playing a role in facilitating chemical reactions.
Used as a Building Block in the Preparation of Various Organic Molecules:
(4-nitrophenyl)phenylphosphinic acid is used as a building block in the preparation of various organic molecules, contributing to the development of a range of chemical compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 5435-78-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5435-78:
(6*5)+(5*4)+(4*3)+(3*5)+(2*7)+(1*8)=99
99 % 10 = 9
So 5435-78-9 is a valid CAS Registry Number.
5435-78-9Relevant academic research and scientific papers
N-hydroxylamines: Influence of Substituents on the Competitive Migration of Aryl and Phenyl Groups in the Lossen-like Rearrangement of their O-Methanesulphonyl Derivatives
Harger, Martin J. P.,Smith, Adrian
, p. 1787 - 1792 (2007/10/02)
The N-hydroxylamines ArPhP(O)NHOH (4) (Ar=p-XC6H4; X=MeO, Me, Cl, NO2) have been prepared from the corresponding phosphinic chlorides (3) using O-(trimethylsilyl)hydroxylamine and converted into the O-methanesulphonyl derivatives
