10055-40-0 Usage
Description
(4-Aminophenyl)(4-fluorophenyl)methanone, with the molecular formula C13H10FNO, is a ketone derivative featuring a phenyl group substituted with both an amino group and a fluorine atom. (4-Aminophenyl)(4-fluorophenyl)methanone is of significant interest to researchers due to its potential applications in various fields, including organic synthesis, medicinal chemistry, and pharmaceutical drug development. Although its precise uses and properties are not yet fully understood, it is anticipated to serve as a valuable building block in the synthesis of a range of organic compounds and as a promising candidate in the development of new pharmaceuticals. Further research is essential to explore and confirm the compound's potential applications and properties.
Uses
Used in Organic Synthesis:
(4-Aminophenyl)(4-fluorophenyl)methanone is used as a building block in organic synthesis for its ability to contribute to the formation of various complex organic compounds. Its unique structure, featuring both an amino and a fluorine substituent, allows for versatile chemical reactions and the creation of a wide array of molecules with different properties and functions.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (4-Aminophenyl)(4-fluorophenyl)methanone is used as a potential drug candidate due to its structural features that may offer specific biological activities. The presence of the amino group can facilitate interactions with biological targets, while the fluorine atom can modulate the compound's lipophilicity and metabolic stability, making it a promising starting point for the design of new therapeutic agents.
Used in Pharmaceutical Drug Development:
(4-Aminophenyl)(4-fluorophenyl)methanone is utilized in pharmaceutical drug development as a precursor or intermediate in the synthesis of novel drugs. Its unique structural elements may confer advantageous pharmacological properties, such as improved binding affinity to target proteins, enhanced selectivity, or reduced side effects. Further research is necessary to fully explore its potential in this application area and to optimize its use in drug discovery processes.
While the specific applications and properties of (4-Aminophenyl)(4-fluorophenyl)methanone are still under investigation, its presence in the scientific community as a compound of interest highlights the potential for future advancements in organic synthesis, medicinal chemistry, and pharmaceutical development. As research progresses, it is expected that the compound will find its niche in these fields, contributing to the creation of innovative and effective products.
Check Digit Verification of cas no
The CAS Registry Mumber 10055-40-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,5 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10055-40:
(7*1)+(6*0)+(5*0)+(4*5)+(3*5)+(2*4)+(1*0)=50
50 % 10 = 0
So 10055-40-0 is a valid CAS Registry Number.
10055-40-0Relevant articles and documents
Coumarin-surfactant modified polyoxometalate catalyzed cross dehydrogenative coupling of benzyl alcohol with the: Para -C-H of unprotected aniline
Xu, Qian,Yu, Gang,Liu, Min,Peng, Chang,Banks, M. Katherine,Xu, Weijian,Wu, Ruoxi,Lu, Yanbing
, p. 5133 - 5136 (2018/10/24)
This paper presents a novel method for synthesizing para-aminobenzophenone and its derivatives (p-ABPs) using a coumarin-surfactant modified polyoxometalate as the catalyst. Preliminary mechanistic studies indicate that the reaction has undergone an oxidative cross dehydrogenative coupling process. This method has the advantages of an easy process, a convenient raw material source, safe and green oxidants, and tolerances of several functional groups.
Efficient Friedel–Crafts benzoylation of aniline derivatives with 4-fluorobenzoyl chloride using copper triflate in the synthesis of aminobenzophenones
Tran, Phuong Hoang,Phung, Huy Quang,Hansen, Poul Erik,Tran, Hai Ngoc,Le, Thach Ngoc
, p. 893 - 901 (2016/07/06)
ABSTRACT: An efficient pathway for the synthesis of the aminobenzophenone derivatives via Friedel–Crafts benzoylation using copper triflate as catalyst is proposed. New derivatives are synthesized. The copper triflate could be easily recovered and reused without loss of catalytic activity. Both the use of ionic liquids and microwave heating turned out to be fruitful.
Synthesis of 4β-N-polyaromatic substituted podophyllotoxins: DNA topoisomerase inhibition, anticancer and apoptosis-inducing activities
Kamal, Ahmed,Kumar, B. Ashwini,Suresh, Paidakula,Agrawal, Satyam Kumar,Chashoo, Gousia,Singh, Shashank K.,Saxena
experimental part, p. 8493 - 8500 (2011/02/24)
A new class of 4β-N-polyaromatic substituted podophyllotoxin congeners have been synthesized and evaluated for their DNA topoisomerase-II (topo-II) inhibition as well as anticancer potential in some human cancer cell lines. The ease of synthesis and inter
