(R)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(allyloxy)-5-oxopentanoic acid

97%

Reagent Code: #37652
fingerprint
CAS Number 204251-86-5

science Other reagents with same CAS 204251-86-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 409.43 g/mol
Formula C₂₃H₂₃NO₆
badge Registry Numbers
MDL Number MFCD01074691
thermostat Physical Properties
Boiling Point 652.3±55.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing complex peptides, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality during the synthesis process. The allyl ester moiety provides additional protection for the carboxyl group, allowing selective deprotection in multi-step reactions. Its application is crucial in solid-phase peptide synthesis (SPPS), enabling the production of peptides with high purity and specificity for use in pharmaceuticals, biochemical research, and drug development. The compound’s design ensures efficient and controlled assembly of peptide chains, making it valuable in the development of therapeutic peptides and protein-based drugs.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to off-white solid
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿5,780.00
inventory 1g
10-20 days ฿1,550.00
inventory 250mg
10-20 days ฿560.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(allyloxy)-5-oxopentanoic acid
No image available
This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing complex peptides, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality during the synthesis process. The allyl ester moiety provides additional protection for the carboxyl group, allowing selective deprotection in multi-step reactions. Its application is crucial in solid-phase peptide synthesis (SPPS), enabling the production of peptides with high purity and specificity for use in pharmaceuticals, biochemical research, and drug development. The compound’s design ensures efficient and controlled assembly of peptide chains, making it valuable in the development of therapeutic peptides and protein-based drugs.
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...