3274-59-7 Usage
Uses
Used in Organic Synthesis:
2,3,4-triphenyl-1H-pyrrole is used as a building block in organic synthesis for the creation of complex organic molecules. Its unique structure and properties allow for the formation of various derivatives, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Research:
2,3,4-triphenyl-1H-pyrrole is used as a potential drug candidate in pharmaceutical research for the treatment of various diseases. Its unique chemical properties and interactions with biological targets make it a promising molecule for the development of new therapeutic agents.
Used in Drug Discovery:
2,3,4-triphenyl-1H-pyrrole is used as a starting point in drug discovery for the identification and optimization of new drug candidates. Its diverse chemical reactivity and potential for modification make it an attractive scaffold for the development of novel therapeutic agents with improved efficacy and selectivity.
Used in Chemical Research:
2,3,4-triphenyl-1H-pyrrole is used as a model compound in chemical research to study the properties and reactivity of phenylpyrroles. This helps in understanding the fundamental aspects of these compounds and their potential applications in various fields, including materials science, catalysis, and supramolecular chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 3274-59-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,7 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3274-59:
(6*3)+(5*2)+(4*7)+(3*4)+(2*5)+(1*9)=87
87 % 10 = 7
So 3274-59-7 is a valid CAS Registry Number.
3274-59-7Relevant academic research and scientific papers
Red-emissive polyphenylated BODIPY derivatives: Effect of peripheral phenyl groups on the photophysical and electrochemical properties
Wakamiya, Atsushi,Sugita, Naoya,Yamaguchi, Shigehiro
supporting information; experimental part, p. 1094 - 1095 (2009/12/03)
A series of red-emissive BODIPY derivatives 2-4 having five to seven phenyl groups on their periphery were synthesized, and their photophysical and electrochemical properties were investigated. While the 8-phenyl-substituted derivatives only have moderate fluorescence quantum yields in solution, they can show intense red fluorescence in the PMMA films. The peripheral phenyl groups also affect the redox reversibility in cyclic voltammetry. Copyright
Samarium(II) iodide-promoted intermolecular and intramolecular ketone- nitrile reductive coupling reactions
Zhou, Longhu,Zhang, Yongmin,Shi, Daqing
, p. 91 - 98 (2007/10/03)
Samarium (II) iodide, a strong one-electron transfer reducing reagent, has been successfully utilized for the intermolecular and intramolecular reductive coupling reactions of ketones with nitriles, α-Hydroxy ketones, monocyclic, fused bicyclic α-hydroxy ketones and monocyclic α-amino alcohols composed of a number of substitution patterns have been prepared in good yields at room temperature or reflux under neutral conditions. The procedure can avoid overreduction of the resulting of α-hydroxy ketones or α-amino alcohols. The crystal structures of monocyclic α-amino alcohols are reported.
