7784-82-9 Usage
Uses
Used in Peptide Synthesis:
Z-PRO-LEU-GLY-OET is used as a building block in peptide synthesis for the creation of larger peptide chains. The protective "Z" group ensures that the amino group of proline is shielded from unwanted side reactions during the synthesis process.
Used in Drug Development:
Z-PRO-LEU-GLY-OET is utilized in drug development as a potential therapeutic agent or as a component of a larger drug molecule. Its specific sequence and protective groups may contribute to the compound's stability, solubility, or biological activity.
Used in Biochemical Research:
Z-PRO-LEU-GLY-OET is employed in biochemical research to study the interactions of amino acids and their derivatives, as well as to investigate the effects of protective groups on the reactivity and properties of peptide compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 7784-82-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,8 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7784-82:
(6*7)+(5*7)+(4*8)+(3*4)+(2*8)+(1*2)=139
139 % 10 = 9
So 7784-82-9 is a valid CAS Registry Number.
InChI:InChI=1/C23H33N3O6/c1-4-31-20(27)14-24-21(28)18(13-16(2)3)25-22(29)19-11-8-12-26(19)23(30)32-15-17-9-6-5-7-10-17/h5-7,9-10,16,18-19H,4,8,11-15H2,1-3H3,(H,24,28)(H,25,29)
7784-82-9Relevant academic research and scientific papers
PROCESS FOR LARGE SCALE LIQUID PHASE SYNTHESIS OF CARBETOCIN AND ITS NOVEL INTERMEDIATES
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, (2017/11/06)
A process for large scale liquid phase synthesis of Carbetocin is disclosed. Novel intermediates of formula (A), formula (B), and processes for their preparation are also disclosed.
PEPTIDE SYNTHESIS BY USING N-ACYLPHOSPHORAMIDITES
Kawanobe, Wataru,Yamaguchi, Kazuo,Nakahama, Seiichi,Yamazaki, Noboru
, p. 825 - 828 (2007/10/02)
New trivalent phosphorus compounds, N-acetyl-N-methylphosphoramidites were prepared readily in good yield by the reaction of phosphorous chlorides and N-methylacetamide.By using the phosphoramidites as condensing agents, Young's peptide and prolyl-leucyl-
Sulfonic acid esters
-
, (2008/06/13)
A novel process for the amidation or esterification which comprises reacting a compound having a carboxy group with a compound having an amino or imino group which can be acylated or with a compound having a hydroxy group in the presence of a sulfonic acid ester of the formula: wherein R1 is an organic group and R2 O-- is a residue of a strongly acidic N-hydroxy compound as a condensation agent, and a novel sulfonic acid ester useful as such a condensation agent and a process for the preparation thereof.
