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Bis[4-(3-aminophenoxy)phenyl] phenylphosphine oxide, commonly known as BAPO-phenyl, is an organic compound with a complex structure that features phenyl, phosphine oxide, and aminophenoxy functional groups. These groups enable a range of chemical reactions and interactions, making it a versatile compound with potential applications in various fields.

132817-72-2

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132817-72-2 Usage

Uses

Used in Advanced Material Science:
Bis[4-(3-aminophenoxy)phenyl] phenylphosphine oxide is used as a reactant or intermediate for the synthesis of other compounds, contributing to the development of advanced materials with unique properties.
Used in Pharmaceutical Industry:
Bis[4-(3-aminophenoxy)phenyl] phenylphosphine oxide is used as a reactant or intermediate in the synthesis of pharmaceutical compounds, potentially leading to the creation of new drugs with improved efficacy and safety profiles.
Due to the complex structure and composition of Bis[4-(3-aminophenoxy)phenyl] phenylphosphine oxide, its detailed applications and properties require rigorous research and testing to fully understand its potential in these industries.

Check Digit Verification of cas no

The CAS Registry Mumber 132817-72-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,8,1 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 132817-72:
(8*1)+(7*3)+(6*2)+(5*8)+(4*1)+(3*7)+(2*7)+(1*2)=122
122 % 10 = 2
So 132817-72-2 is a valid CAS Registry Number.

132817-72-2Downstream Products

132817-72-2Relevant academic research and scientific papers

Structural effects of the monomer type on the properties of copolyimides and copolyimide-silica hybrid materials

Kizilkaya, Canan,Bicen, Merve,Karatas, Sevim,Gungor, Atilla

, p. 1061 - 1071 (2015/11/27)

In this work, the effects of two different diamine monomers containing phosphine oxide on the thermal, mechanical and morphological properties of copolyimides and their hybrid materials were investigated. The gas separation properties of the synthesized copolyimides were also analyzed. The two different diamine monomers containing phosphine oxide were bis(3-aminophenyl]phenylphosphine oxide (BAPPO) and bis[4-(3-aminophenoxy)phenyl)phenylphosphine oxide (m-BAPPO). In the synthesis of the copolyimides, 3,3'-diaminodiphenyl sulfone (3,3'-DDS) was also used as the diamine, as well as 2,2-bis(3,4-dicarboxyphenyl)hexafluoropropane dianhydride (6FDA). Copolyimide films were prepared by thermal imidization. Furthermore, hybrid materials containing 5 % SiO2 were synthesized by the sol-gel technique. Fourier-transform infrared spectroscopy (FTIR) and nuclear magnetic resonance spectroscopy (NMR) confirmed the expected structures. Dynamic mechanical analysis (DMA) demonstrated that the m-BAPPO-based copolyimides had lower glass transition temperatures (Tg) than the BAPPO-based ones. The thermal decomposition temperature of the m-BAPPO-containing copolyimide without silica was shifted to a higher value. The moduli and strength values of the BAPPO diamine-containing copolyimide and its hybrid were higher than those of the m-BAPPO-containing materials. Contact angle measurements showed their hydrophobicity. Scanning electron microscope (SEM) analysis showed the dispersion of the silica particles in the copolyimides. These copolyimides may be used in the coating industry. The CO2 permeability and the permselectivity were the highest, among the other values found in this study, when the m-BAPPO-containing copolyimide in the absence of silica was used. The gas permeabilities obtained from this work were in the decreasing order: PCO2 > > PO2 > PN2.

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