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L-Serine, N-(2,4-dinitrophenyl)-, methyl ester is a chemical compound derived from L-serine, an amino acid that plays a crucial role in various biological processes. This specific compound is characterized by the presence of a 2,4-dinitrophenyl group attached to the nitrogen atom of the serine molecule, and a methyl ester group attached to the carboxylic acid group. The 2,4-dinitrophenyl group is known for its strong chromophore properties, making it useful in spectroscopic studies and as a reporter group in various biochemical assays. The methyl ester group, on the other hand, provides a protected form of the carboxylic acid, which can be hydrolyzed under specific conditions to regenerate the free acid. L-Serine, N-(2,4-dinitrophenyl)-, methyl ester is often used in research settings to study protein-ligand interactions and enzyme kinetics, as well as in the development of new drugs and diagnostic tools. Its unique structure allows for specific binding and recognition events, making it a valuable tool in the field of biochemistry and molecular biology.

5183-32-4

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5183-32-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5183-32-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,8 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5183-32:
(6*5)+(5*1)+(4*8)+(3*3)+(2*3)+(1*2)=84
84 % 10 = 4
So 5183-32-4 is a valid CAS Registry Number.

5183-32-4Downstream Products

5183-32-4Relevant academic research and scientific papers

Synthesis of o-Nitroarylamines via Ipso Nucleophilic Substitution of Sulfonic Acids

Manne, Srinivasa Rao,Chandra, Jyoti,Mandal, Bhubaneswar

supporting information, p. 636 - 639 (2019/01/21)

A mild, efficient, and eco-friendly method for the synthesis of o-nitroarylamine from o-nitroaryl sulfonic acid via ipso nucleophilic aryl substitution by amine is described. The products have been obtained with good yields at room temperature without the assistance of any metal, activating agent, or toxic oxidant. This method is useful for racemization-free synthesis of N-aryl amino acid esters.

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