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(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.

524698-40-6

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524698-40-6 Usage

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 academic research and scientific papers

A facile transformation of amino acids to functionalized coumarins

Bandyopadhyay, Anupam,Gopi, Hosahudya N.

supporting information; experimental part, 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 method for manufacturing optically active coumaryl amino acid salts and the coumaryl aminoacid salts thus obtained

-

Page/Page column 19, (2010/02/13)

The present invention relates to the field of the synthesis of optically active amino acids, mainly for the purpose of manufacturing optically active polypeptides that are useful as labelled detection tools. The manufacturing method involves the preparati

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

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