CAS:129223-22-9 | Fmoc-Pro-Pro-OH

Introduction and application of CAS 129223-22-9 | Fmoc-Pro-Pro-OH

Fmoc-Pro-Pro-OH is a peptide that is synthesized by the solid phase and liquid phase methods. The synthesis process of this peptide can be divided into three steps: (i) Acidification, (ii) Nucleophilic substitution, and (iii) Deprotection. The first step involves the conversion of N-(tertbutyldimethylsilyloxy)-L-(2-(mercaptomethyl)-1,3-dioxolan-4-yl)alanine to its corresponding carboxylic acid in methanol with tetrahydrofuran as a co solvent. The second step includes the nucleophilic substitution of the carboxylic acid with 2-(chloromethyl

Synonyms:

(2S)-1-[(2S)-1-(9H-fluoren-9-ylmethoxycarbonyl)pyrrolidine-2-carbonyl]pyrrolidine-2-carboxylic acid;

N-Fmoc-L-prolyl-L-proline;

Specification of CAS 129223-22-9 | Fmoc-Pro-Pro-OH

Package and transportation of Introduction and application of CAS 129223-22-9 | Fmoc-Pro-Pro-OH

Package:0.1g,1g,5g,25g,100g,500g,1kg

Transportation: by courier/ by air/ by sea

Related Articles of CAS 129223-22-9 | Fmoc-Pro-Pro-OH

On the role of basic residues of head-to-tail cyclic bradykinin analogues on rat duodenum relaxation

M Gobbo, L Biondi, F Filira, R Rocchi, T Piek - Letters in Peptide Science, 2000 - Springer

… consequent peptide chain loss in the form of diketopiperazine [10], was prevented either by

growing the peptide on the TCP resin or by using the dipeptide Fmoc-Pro-Pro-OH in the first …

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