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L-Valine, N-[N-[(phenylmethoxy)carbonyl]-L-isoleucyl]-, methyl ester is a complex organic compound with the chemical formula C19H25NO4. It is a derivative of the amino acid L-valine, featuring an N-[N-[(phenylmethoxy)carbonyl]-L-isoleucyl] group attached to the L-valine molecule. The methyl ester functional group is present, indicating that the compound has a methyl group attached to the carboxylic acid group, making it an ester. L-Valine, N-[N-[(phenylmethoxy)carbonyl]-L-isoleucyl]-, methyl ester is of interest in the field of peptide chemistry and may have potential applications in pharmaceuticals or as a building block for more complex molecules. Its structure and properties make it a valuable component in the synthesis of certain drugs and bioactive compounds, particularly those involving peptide bonds.

4818-02-4

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4818-02-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4818-02-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,1 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4818-02:
(6*4)+(5*8)+(4*1)+(3*8)+(2*0)+(1*2)=94
94 % 10 = 4
So 4818-02-4 is a valid CAS Registry Number.

4818-02-4Relevant academic research and scientific papers

Tandem deprotection/coupling for peptide synthesis in water at room temperature

Cortes-Clerget, Margery,Berthon, Jean-Yves,Krolikiewicz-Renimel, Isabelle,Chaisemartin, Laurent,Lipshutz, Bruce H.

supporting information, p. 4263 - 4267 (2017/09/28)

A tandem deprotection/coupling sequence is reported for solution-phase peptide synthesis in water under micellar catalysis conditions using the designer surfactant TPGS-750-M. Cbz deprotection followed by peptide coupling in the presence of COMU and 2,6-lutidine afforded polypeptides containing up to 10 amino acid residues. A broad scope characterizes this new technology. No epimerization has been detected. The associated E Factors, as a measure of "greenness" and known to be extremely high for peptide couplings, have been reduced to less than 10 due to the step-economy and minimal amounts of organic solvent needed for product extraction.

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