55076-19-2 Usage
Uses
Used in Medicinal Chemistry:
Phenyl(3-phenyl-1H-indazol-1-yl)methanone is used as a compound of interest in medicinal chemistry for its potential biological activities. The presence of the indazole ring, which is known to exhibit antimicrobial, antiviral, anticancer, and anti-inflammatory properties, makes it a candidate for further exploration in drug development.
Used in Antimicrobial Applications:
In the field of antimicrobial research, phenyl(3-phenyl-1H-indazol-1-yl)methanone is considered for its potential to combat various microorganisms due to the antimicrobial properties often associated with indazole compounds.
Used in Antiviral Applications:
Phenyl(3-phenyl-1H-indazol-1-yl)methanone may be utilized as an antiviral agent, leveraging the antiviral characteristics of indazoles to inhibit viral replication or infectivity.
Used in Anticancer Applications:
phenyl(3-phenyl-1H-indazol-1-yl)methanone is also eyed for its possible role in cancer treatment, as indazoles have shown anticancer properties. Phenyl(3-phenyl-1H-indazol-1-yl)methanone could be developed to target and inhibit the growth of cancer cells.
Used in Anti-inflammatory Applications:
Given the anti-inflammatory potential of indazoles, phenyl(3-phenyl-1H-indazol-1-yl)methanone might be employed in the development of anti-inflammatory drugs, which could help manage inflammation and related conditions.
While the specific applications and efficacy of phenyl(3-phenyl-1H-indazol-1-yl)methanone are yet to be fully investigated, its chemical structure and the known properties of related indazole compounds provide a foundation for its potential use across various therapeutic areas. Further research is necessary to determine its exact role and effectiveness in these applications.
Check Digit Verification of cas no
The CAS Registry Mumber 55076-19-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,0,7 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 55076-19:
(7*5)+(6*5)+(5*0)+(4*7)+(3*6)+(2*1)+(1*9)=122
122 % 10 = 2
So 55076-19-2 is a valid CAS Registry Number.
55076-19-2Relevant academic research and scientific papers
Unorthodox cascade reaction of arynes and: N -nitrosamides leading to indazole scaffolds
Baidya, Mahiuddin,Bhajammanavar, Vinod,Choutipalli, Venkata Surya Kumar,Subramanian, Venkatesan,Sureshbabu, Popuri
supporting information, p. 1187 - 1190 (2022/02/03)
An unusual cascade annulation of arynes with N-alkyl-N-nitrosamides is developed by leveraging aryne σ-insertion and C(sp3)-H bond functionalization strategies under transition-metal-free conditions at ambient temperature, offering functionalized indazoles in high yields and regioselectivity. The protocol is scalable and exhibits a broad substrate scope. The reaction mechanism is also studied with DFT calculations.
Synthesis of indazoles by the [3+2] cycloaddition of diazo compounds with arynes and subsequent acyl migration
Liu, Zhijian,Shi, Feng,Martinez, Pablo D. G.,Raminelli, Cristiano,Larock, Richard C.
, p. 219 - 226 (2008/09/17)
(Chemical Equation Presented) The [3+2] cycloaddition of a variety of diazo compounds with o-(trimethylsilyl)aryl triflates in the presence of CsF or TBAF at room temperature provides a very direct, efficient approach to a wide range of potentially biologically and pharmaceutically interesting substituted indazoles in good to excellent yields under mild reaction conditions. Simple diazomethane derivatives afford N-unsubstituted indazoles or 1-arylated indazoles, depending upon the stoichiometry of the reagents and the reaction conditions, while dicarbonyl-containing diazo compounds undergo carbonyl migration to afford 1-acyl or 1-alkoxycarbonyl indazoles selectively.
