524698-40-6 Usage
Description
(S)-2-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-3-(7-METHOXY-2-OXO-2H-CHROMEN-4-YL)-PROPIONIC ACID is a complex chemical compound that belongs to the class of propionic acids. It is characterized by the presence of a fluorene moiety, a chromen-4-yl group, and a methoxy carbonylamino group. (S)-2-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-3-(7-METHOXY-2-OXO-2H-CHROMEN-4-YL)-PROPIONIC ACID holds potential for biological activities and is of interest in the fields of pharmaceutical research and drug development. Further studies and experimentation are necessary to explore its specific properties and potential applications.
Uses
Used in Pharmaceutical Research:
(S)-2-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-3-(7-METHOXY-2-OXO-2H-CHROMEN-4-YL)-PROPIONIC ACID is used as a compound of interest for its potential biological activities in the field of pharmaceutical research. (S)-2-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-3-(7-METHOXY-2-OXO-2H-CHROMEN-4-YL)-PROPIONIC ACID's unique structure and properties make it a candidate for further investigation into its possible therapeutic uses.
Used in Drug Development:
In the industry of drug development, (S)-2-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-3-(7-METHOXY-2-OXO-2H-CHROMEN-4-YL)-PROPIONIC ACID is utilized as a starting material or a structural component in the design and synthesis of new drugs. Its potential role in creating novel therapeutic agents is being explored through ongoing research and development efforts.
Check Digit Verification of cas no
The CAS Registry Mumber 524698-40-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,2,4,6,9 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 524698-40:
(8*5)+(7*2)+(6*4)+(5*6)+(4*9)+(3*8)+(2*4)+(1*0)=176
176 % 10 = 6
So 524698-40-6 is a valid CAS Registry Number.
524698-40-6Relevant articles and documents
A facile transformation of amino acids to functionalized coumarins
Bandyopadhyay, Anupam,Gopi, Hosahudya N.
, p. 8089 - 8095 (2012/01/04)
The synthesis of novel chiral coumarins functionalized with proteinogenic amino acid side chains via N-protected γ-amino-β-keto esters and their incorporation into the cell permeable HIV-1 TAT peptide through the modified solid phase peptide synthesis are
A very short route to enantiomerically pure coumarin-bearing fluorescent amino acids
Brun, Marie-Priscille,Bischoff, Laurent,Garbay, Christiane
, p. 3432 - 3436 (2007/10/03)
No bulkier than a tryptophan or a tyrosine residue are the fluorescent coumaryl amino acids described. These building blocks can be synthesized rapidly with high enantiomeric purity and introduced readily into a peptidic sequence. Their fluorescence prope
