(2S,4R)-Fmoc-4-(4-fluorobenzyl)pyrrolidine-2-carboxylic acid

97%

Reagent Code: #36546
fingerprint
CAS Number 959576-18-2

science Other reagents with same CAS 959576-18-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 445.4800 g/mol
Formula C₂₇H₂₄NO₄F
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amine functionality during the synthesis process. The 4-(4-fluorobenzyl) substitution on the pyrrolidine ring can influence the peptide's conformational properties, potentially enhancing its biological activity or stability. This chemical is especially valuable in the development of peptide-based pharmaceuticals, where precise control over amino acid incorporation is crucial. Its application is also relevant in research focused on designing peptides with specific structural or functional properties, such as enzyme inhibitors or receptor ligands.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,273.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(2S,4R)-Fmoc-4-(4-fluorobenzyl)pyrrolidine-2-carboxylic acid
No image available

This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amine functionality during the synthesis process. The 4-(4-fluorobenzyl) substitution on the pyrrolidine ring can influence the peptide's conformational properties, potentially enhancing its biological activity or stability. This chemical is especial

This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amine functionality during the synthesis process. The 4-(4-fluorobenzyl) substitution on the pyrrolidine ring can influence the peptide's conformational properties, potentially enhancing its biological activity or stability. This chemical is especially valuable in the development of peptide-based pharmaceuticals, where precise control over amino acid incorporation is crucial. Its application is also relevant in research focused on designing peptides with specific structural or functional properties, such as enzyme inhibitors or receptor ligands.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...