582299-76-1 Usage
Uses
Used in Organic Synthesis:
2,4-Cyclopentadien-1-one, 3,4-bis(4-aminophenyl)-2,5-diphenylis utilized as a key intermediate in organic synthesis for the creation of various complex organic molecules. Its versatile structure allows for multiple points of chemical modification, facilitating the synthesis of a wide range of compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2,4-Cyclopentadien-1-one, 3,4-bis(4-aminophenyl)-2,5-diphenylis employed as a starting material for the development of new drugs. Its unique molecular structure and potential pharmacological properties make it a promising candidate for the treatment of various diseases. Researchers are exploring its use in the design of novel therapeutic agents that can target specific biological pathways or receptors.
Used in Chemical Research:
2,4-Cyclopentadien-1-one, 3,4-bis(4-aminophenyl)-2,5-diphenylalso serves as a subject of interest in fundamental chemical research. Scientists are investigating its chemical properties, reactivity, and potential applications in various chemical processes. This research can lead to a better understanding of the compound's behavior and open up new avenues for its utilization in different fields.
Check Digit Verification of cas no
The CAS Registry Mumber 582299-76-1 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 582299-76:
(8*5)+(7*8)+(6*2)+(5*2)+(4*9)+(3*9)+(2*7)+(1*6)=201
201 % 10 = 1
So 582299-76-1 is a valid CAS Registry Number.
582299-76-1Relevant 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.
