582299-75-0 Usage
Uses
Used in Organic Synthesis:
2,4-Cyclopentadien-1-one, 3-(4-aminophenyl)-2,4,5-triphenylis used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure allows for versatile chemical reactions, making it a valuable building block in the synthesis of complex molecules.
Used in Pharmaceutical Industry:
2,4-Cyclopentadien-1-one, 3-(4-aminophenyl)-2,4,5-triphenylis used as a key component in the development of pharmaceuticals. Its presence of an amino group and phenyl rings can be exploited to create new drug candidates with potential therapeutic properties. 2,4-Cyclopentadien-1-one, 3-(4-aminophenyl)-2,4,5-triphenylcan be further modified or used as a precursor to synthesize bioactive molecules for treating various diseases.
Used in Material Science:
2,4-Cyclopentadien-1-one, 3-(4-aminophenyl)-2,4,5-triphenylis used as a functional material in material science. Its unique structure and properties can be utilized to develop new materials with specific characteristics, such as conductivity, stability, or optical properties. 2,4-Cyclopentadien-1-one, 3-(4-aminophenyl)-2,4,5-triphenylcan be incorporated into polymers, coatings, or other materials to enhance their performance or introduce new functionalities.
Check Digit Verification of cas no
The CAS Registry Mumber 582299-75-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,2,2,9 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 582299-75:
(8*5)+(7*8)+(6*2)+(5*2)+(4*9)+(3*9)+(2*7)+(1*5)=200
200 % 10 = 0
So 582299-75-0 is a valid CAS Registry Number.
582299-75-0Relevant academic research and scientific papers
Peptide-functionalized polyphenylene dendrimers
Herrmann, Andreas,Mihov, Gueorgui,Vandermeulen, Guido W. M.,Klok, Harm-Anton,Müllen, Klaus
, p. 3925 - 3935 (2007/10/03)
This contribution describes the synthesis of polyphenylene dendrimers that are functionalized with up to 16 lysine residues or substituted with short peptide sequences composed of 5 lysine or glutamic acid repeats and a C- or N-terminal cysteine residue. Polyphenylene dendrimers were prepared via a sequence of Diels-Alder cycloaddition and deprotection reactions from cyclopentadienone building blocks. Single amino acids could be introduced on the periphery of the dendrimers by using amino acid substituted cyclopentadienones in the last Diels-Alder addition reaction. Alternatively, peptide sequences were attached via a chemoselective reaction, which involved the addition of the sulfhydryl group of a cysteine residue of an oligopeptide to a maleimide moiety present on the surface of the dendrimer. These amino acid and peptide functionalized dendrimers may be of interest as model compounds to study DNA complexation and condensation or as building blocks for the preparation of novel supramolecular architectures via layer-by-layer self-assembly.
