2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(5-methoxy-1H-indol-3-yl)propanoic acid

97%

Reagent Code: #41093
fingerprint
CAS Number 138775-54-9

science Other reagents with same CAS 138775-54-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 456.49 g/mol
Formula C₂₇H₂₄N₂O₅
badge Registry Numbers
MDL Number MFCD02682367
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily used in peptide synthesis, particularly solid-phase peptide synthesis (SPPS), as a protected amino acid derivative. It serves as a building block for constructing peptide chains, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amino functionality. The indole moiety in its structure makes it particularly useful for incorporating tryptophan analogs into peptides, which are essential for studying protein interactions and designing bioactive molecules. Its application is significant in pharmaceutical research, especially in the development of peptide-based drugs and biochemical studies involving tryptophan-rich proteins.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿20,007.00
inventory 100mg
10-20 days ฿9,999.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(5-methoxy-1H-indol-3-yl)propanoic acid
No image available

This compound is primarily used in peptide synthesis, particularly solid-phase peptide synthesis (SPPS), as a protected amino acid derivative. It serves as a building block for constructing peptide chains, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amino functionality. The indole moiety in its structure makes it particularly useful for incorporating tryptophan analogs into peptides, which are essential for studying protein interactions and designing bioactive molec

This compound is primarily used in peptide synthesis, particularly solid-phase peptide synthesis (SPPS), as a protected amino acid derivative. It serves as a building block for constructing peptide chains, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amino functionality. The indole moiety in its structure makes it particularly useful for incorporating tryptophan analogs into peptides, which are essential for studying protein interactions and designing bioactive molecules. Its application is significant in pharmaceutical research, especially in the development of peptide-based drugs and biochemical studies involving tryptophan-rich proteins.

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...