138774-86-4

Usage

Molecular Structure

A complex organic molecule consisting of a 9H-fluorenylmethyl ester group, a 2-(chlorocarbonyl) group, and a 1-piperidinecarboxylic acid group.

Functional Groups

Key functional groups present in the molecule include an ester group (-COO-), an amide group (-CONH-), and a piperidine ring.

Chirality

The compound is chiral, with the (S)-configuration indicating the specific spatial arrangement of the molecule.

Use in Synthesis

Fmoc-S-Pip-OH is commonly used as a building block in the synthesis of peptides and small molecule drugs, particularly in solid-phase peptide synthesis.

Protecting Group

It serves as a protecting group for the N-terminal of amino acids during peptide synthesis, which allows for the stepwise assembly of peptides.

Unique Structure and Reactivity

The compound's structure and reactivity make it a valuable tool in the development of new pharmaceuticals and biologically active molecules.

Applications

Fmoc-S-Pip-OH is used in the fields of organic chemistry, peptide synthesis, and drug development.

Downstream Products

• 138775-33-4 Fmoc-D-Phe-L-Ile-D-Pip-L-Pip-D-(N-allyl)Phe-L-Pro-OCH₂Ph 
• 144073-44-9 Cbz-D-Phe-L-Ile-D-(N^δ-Cbz)Piz-L-Pip-D-(N-Me)Phe-L-Pro-OCH2Ph 
• 138774-78-4 Fmoc-D-Phe-L-Ile-D-Pro-L-Pip-D-(N-Me)Phe-L-Pro-OCH₂Ph 
• 144073-43-8 Fmoc-L-Ile-D-(N^δ-Cbz)Piz-L-Pip-D-(N-Me)Phe-L-Pro-OCH2Ph 
• 144073-32-5 Cbz-D-Phe-L-Ile-D-Pip-L-Pip-D-Phe-L-Pro-OCH₂Ph 
• 144073-33-6 Fmoc-L-Ile-D-Pip-L-Pip-D-(N-allyl)Phe-L-Pro-OCH₂Ph 
• 144073-31-4 Fmoc-L-Ile-D-Pip-L-Pip-D-Phe-L-Pro-OCH₂Ph 
• 138774-81-9 H-D-Phe-L-Ile-D-Pro-L-Pip-D-(N-Me)Phe-L-Pro-OCH₂Ph 
• 144073-24-5 Fmoc-D-Pro-L-Pip-D-(N-Me)Phe-L-Pro-OCH₂Ph