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3-[(2,4-dinitrophenyl)disulfanyl]propanoic acid is a complex organic compound characterized by its unique chemical structure. It features a propane carboxylic acid backbone, with a disulfide bridge connecting a 2,4-dinitrophenyl group. The 2,4-dinitrophenyl moiety is known for its strong electron-withdrawing properties, which can significantly influence the reactivity and stability of the compound. This molecule is of interest in various fields, including chemistry and materials science, due to its potential applications in the synthesis of dyes, pharmaceuticals, and other specialty chemicals. Its specific properties, such as solubility and reactivity, can be tailored for specific uses, making it a versatile building block in organic synthesis.

3513-48-2

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3513-48-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3513-48-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,1 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3513-48:
(6*3)+(5*5)+(4*1)+(3*3)+(2*4)+(1*8)=72
72 % 10 = 2
So 3513-48-2 is a valid CAS Registry Number.

3513-48-2Relevant academic research and scientific papers

Peptide-bond Formation, Chemoselective Acylation of Amino Acids, and Crosslinking Reaction between Amino Acids Utilizing a Functional Five-membered Heterocycle, 1,3-Thiazolidine-2-thione

Nagao, Yoshimitsu,Miyasaka, Tadayo,Seno, Kaoru,Fujita, Eiichi,Shibata, Daisuke,Doi, Etsushiro

, p. 2439 - 2446 (2007/10/02)

The monitored aminolysis of 3-acyl-1,3-thiazolidine-2-thiones has been extended to the peptide-bond formation, the chemoselective acylation of amino acids having multifunctional groups, and the crosslinking reaction between amino acids.

MONITORED AMINOLYSIS OF 3-ACYL-1,3-THIAZOLIDINE-2-THIONE WITH AMINO ACID AND ITS DERIVATIVE: PEPTIDE BOND FORMATION, CHEMOSELECTIVE ACYLATION, AND BRIDGING REACTION

Nagao, Yoshimitsu,Miyasaka, Tadayo,Seno, Kaoru,Yagi, Masahiro,Fujita, Eiichi

, p. 463 - 466 (2007/10/02)

As a new extention of the monitored aminolysis of 3-acyl-1,3-thiazolidine-2-thione, its applications to peptide bond formation, chemoselective acylation of amino acid, and bridging reaction on the enzyme model are reported.

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