(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3,3-dimethylpentanoicacid

97%

Reagent Code: #237752
fingerprint
CAS Number 1227750-73-3

science Other reagents with same CAS 1227750-73-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 367.44 g/mol
Formula C₂₂H₂₅NO₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in peptide synthesis as a protected amino acid derivative, this compound enables the controlled assembly of complex peptides by preventing unwanted side reactions. The Fmoc group allows for mild base-induced deprotection, making it compatible with solid-phase synthesis strategies. Its steric bulk helps improve selectivity and reduce racemization during coupling steps. Commonly employed in the production of pharmaceutical peptides, research reagents, and biochemical probes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,620.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3,3-dimethylpentanoicacid
No image available

Used primarily in peptide synthesis as a protected amino acid derivative, this compound enables the controlled assembly of complex peptides by preventing unwanted side reactions. The Fmoc group allows for mild base-induced deprotection, making it compatible with solid-phase synthesis strategies. Its steric bulk helps improve selectivity and reduce racemization during coupling steps. Commonly employed in the production of pharmaceutical peptides, research reagents, and biochemical probes.

Used primarily in peptide synthesis as a protected amino acid derivative, this compound enables the controlled assembly of complex peptides by preventing unwanted side reactions. The Fmoc group allows for mild base-induced deprotection, making it compatible with solid-phase synthesis strategies. Its steric bulk helps improve selectivity and reduce racemization during coupling steps. Commonly employed in the production of pharmaceutical peptides, research reagents, and biochemical probes.

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...