(S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-bromo-5-fluorophenyl)propanoic acid

95%

Reagent Code: #38014
fingerprint
CAS Number 2278366-87-1

science Other reagents with same CAS 2278366-87-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 484.31 g/mol
Formula C₂₄H₁₉BrFNO₄
inventory_2 Storage & Handling
Density 1.495±0.06 g/cm3(Predicted)
Storage RT

description Product Description

This compound is primarily used in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protective group for the amine functionality, allowing selective deprotection during solid-phase peptide synthesis. The bromo and fluoro substituents on the phenyl ring make it a valuable building block for introducing specific structural motifs into peptides, particularly in the development of bioactive molecules or pharmaceuticals. Its application is significant in medicinal chemistry for designing peptide-based drugs, where precise control over amino acid incorporation is essential. Additionally, the bromine atom can be utilized in further functionalization reactions, such as cross-coupling, to create more complex structures.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿62,100.00
inventory 250mg
10-20 days ฿31,050.00
inventory 100mg
10-20 days ฿18,900.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-bromo-5-fluorophenyl)propanoic acid
No image available
This compound is primarily used in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protective group for the amine functionality, allowing selective deprotection during solid-phase peptide synthesis. The bromo and fluoro substituents on the phenyl ring make it a valuable building block for introducing specific structural motifs into peptides, particularly in the development of bioactive molecules or pharmaceuticals. Its application is significant in medicinal chemistry for designing peptide-based drugs, where precise control over amino acid incorporation is essential. Additionally, the bromine atom can be utilized in further functionalization reactions, such as cross-coupling, to create more complex structures.
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...