54300-32-2 Usage
Description
BIS(4-FLUOROPHENYL)PHENYLPHOSPHINE OXIDE is an organic compound that serves as a versatile catalyst and additive in various chemical processes and materials. It is known for its ability to enhance the efficiency and performance of different applications.
Uses
Used in Chemical Industry:
BIS(4-FLUOROPHENYL)PHENYLPHOSPHINE OXIDE is used as a catalyst for hydroformylation reactions, which are essential in the production of aldehydes and alcohols, key components in the synthesis of various chemicals and pharmaceuticals.
Used in Desalination Industry:
BIS(4-FLUOROPHENYL)PHENYLPHOSPHINE OXIDE is used for the preparation of chlorine-tolerant polymers, which are crucial in the development of desalination technologies. These polymers help in the removal of salt and other impurities from water, making it suitable for various applications, including drinking and irrigation.
Used in Fuel Cell Industry:
BIS(4-FLUOROPHENYL)PHENYLPHOSPHINE OXIDE is used as a crosslinking agent in the preparation of polymer electrolyte membranes for fuel cell applications. These membranes play a vital role in the efficient functioning of fuel cells, which are widely used in electric vehicles and energy storage systems.
Check Digit Verification of cas no
The CAS Registry Mumber 54300-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,3,0 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54300-32:
(7*5)+(6*4)+(5*3)+(4*0)+(3*0)+(2*3)+(1*2)=82
82 % 10 = 2
So 54300-32-2 is a valid CAS Registry Number.
InChI:InChI=1/C18H13F2OP/c19-14-6-10-17(11-7-14)22(21,16-4-2-1-3-5-16)18-12-8-15(20)9-13-18/h1-13H
54300-32-2Relevant articles and documents
Visible-Light Driven C-P Bond Formation with Recyclable Carbon Nitride Photocatalyst
Guo, Wusheng,Liu, Yang
, (2022/05/12)
The development of metal-free chemical process with recyclable heterogeneous catalyst under ambient conditions is highly desired in industrial production, especially for pharmaceutical purpose. We herein reported the efficient synthesis of pharmaceuticall
Aryltrimethylammonium Tetrafluoroborates in Nickel-Catalyzed C–P Bond-Forming Reactions
Li, Chun Jing
, p. 954 - 960 (2021/07/22)
Abstract: The first nickel-catalyzed phosphorylation of aryltrimethylammonium tetrafluoroborates with the formation of C–P bond instead of C–N has been developed. Starting from easily available and inexpensive aromatic amines, a variety of important arylphosphonates have been synthesized in moderate to excellent yields.
Photoinduced Transition-Metal-Free Cross-Coupling of Aryl Halides with H-Phosphonates
Zeng, Huiying,Dou, Qian,Li, Chao-Jun
supporting information, p. 1301 - 1305 (2019/02/19)
Photoinduced transition-metal- and photosensitizer-free cross-coupling of aryl halides (including Ar-Cl, Ar-Br, and Ar-I) with H-phosphonates (including dialkyl phosphonates and diarylphosphine oxides) is reported. Various functional groups were tolerated, including ester, methoxy, dimethoxy, alkyl, phenyl, trifluoromethyl, and heterocyclic compounds. This simple and green strategy provides a practical pathway to synthesize arylphosphine oxides.
