767288-75-5 Usage
Uses
Used in Organic Synthesis:
(2-bromo-4-nitrophenyl)(phenyl)methanone is used as a building block in organic synthesis for the creation of a wide range of chemical compounds. Its unique structure allows for further functionalization and modification, facilitating the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In pharmaceutical research, (2-bromo-4-nitrophenyl)(phenyl)methanone is utilized as a starting material for the development of new drugs. Its chemical properties make it a promising candidate for the synthesis of biologically active compounds with potential therapeutic applications.
Used as a Photoinitiator in Polymer Production:
(2-bromo-4-nitrophenyl)(phenyl)methanone has been studied for its potential application as a photoinitiator in the production of polymer materials. Its ability to initiate polymerization reactions upon exposure to light makes it a valuable component in the manufacturing of various polymer-based products.
Used in the Synthesis of Biologically Active Compounds:
(2-bromo-4-nitrophenyl)(phenyl)methanone is also used as a precursor in the synthesis of various biologically active compounds. Its presence in the molecular structure can contribute to the biological activity of the final product, making it an important component in the development of pharmaceuticals and other bioactive substances.
Check Digit Verification of cas no
The CAS Registry Mumber 767288-75-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,7,2,8 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 767288-75:
(8*7)+(7*6)+(6*7)+(5*2)+(4*8)+(3*8)+(2*7)+(1*5)=225
225 % 10 = 5
So 767288-75-5 is a valid CAS Registry Number.
767288-75-5Relevant academic research and scientific papers
Aerobic oxidative acylation of nitroarenes with arylacetic esters under mild conditions: Facile access to diarylketones
Li, Jiang-Sheng,Yang, Qian,Yang, Fan,Chen, Guo-Qin,Li, Zhi-Wei,Kuang, Yin-Jie,Zhang, Wei-Jing,Huang, Peng-Mian
, p. 140 - 145 (2017/12/27)
A facile and regioselective base-mediated aerobic oxidative acylation of nitroarenes to access diarylketones under mild conditions has been developed. It features the use of bench-stable and readily available arylacetates as acyl surrogates, and the absence of transition-metals and synthetic oxidants. This protocol involves a cascade CDC/oxidative decarboxylation process.
Synthesis of 3-substituted indazoles and benzoisoxazoles via Pd-catalyzed cyclization reactions: application to the synthesis of nigellicine
Inamoto, Kiyofumi,Katsuno, Mika,Yoshino, Takashi,Arai, Yukari,Hiroya, Kou,Sakamoto, Takao
, p. 2695 - 2711 (2007/10/03)
Syntheses of 3-substituted indazoles and benzoisoxazoles were efficiently accomplished with the aid of Pd-catalyzed intramolecular carbon-nitrogen and carbon-oxygen bond formations. The catalyst system described herein allows the cyclization to proceed under very mild conditions and thus could be applied to a wide range of substrates with acid- or base-sensitive functional groups. A total synthesis for the indazole ring-containing natural product nigellicine is also described.
