(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-phenylpropanoic acid

95%

Reagent Code: #38364
fingerprint
CAS Number 1217663-60-9

science Other reagents with same CAS 1217663-60-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 387.4279 g/mol
Formula C₂₄H₂₁NO₄
badge Registry Numbers
MDL Number MFCD12198213
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This is the Fmoc-protected form of L-phenylalanine (Fmoc-Phe-OH), a key building block in peptide synthesis. The fluorenylmethoxycarbonyl (Fmoc) group protects the N-terminal amino group, enabling its use in solid-phase peptide synthesis (SPPS). During SPPS, the carboxylic acid couples to the growing peptide chain, and the Fmoc group is selectively removed under mild basic conditions (e.g., with piperidine) to allow the next amino acid to be added, facilitating stepwise assembly without side reactions. This compound is crucial for producing custom peptides in pharmaceutical research, drug development, and biochemical applications. Its orthogonal protection strategy and stability make it ideal for synthesizing complex biomolecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,362.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-phenylpropanoic acid
No image available
This is the Fmoc-protected form of L-phenylalanine (Fmoc-Phe-OH), a key building block in peptide synthesis. The fluorenylmethoxycarbonyl (Fmoc) group protects the N-terminal amino group, enabling its use in solid-phase peptide synthesis (SPPS). During SPPS, the carboxylic acid couples to the growing peptide chain, and the Fmoc group is selectively removed under mild basic conditions (e.g., with piperidine) to allow the next amino acid to be added, facilitating stepwise assembly without side reactions. This
This is the Fmoc-protected form of L-phenylalanine (Fmoc-Phe-OH), a key building block in peptide synthesis. The fluorenylmethoxycarbonyl (Fmoc) group protects the N-terminal amino group, enabling its use in solid-phase peptide synthesis (SPPS). During SPPS, the carboxylic acid couples to the growing peptide chain, and the Fmoc group is selectively removed under mild basic conditions (e.g., with piperidine) to allow the next amino acid to be added, facilitating stepwise assembly without side reactions. This compound is crucial for producing custom peptides in pharmaceutical research, drug development, and biochemical applications. Its orthogonal protection strategy and stability make it ideal for synthesizing complex biomolecules.
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...