2-(1-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)cyclopropyl)acetic acid

98%

Reagent Code: #198052
fingerprint
CAS Number 1219953-64-6

science Other reagents with same CAS 1219953-64-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 337.37 g/mol
Formula C₂₀H₁₉NO₄
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily in peptide synthesis as a protected amino acid building block, this compound enables the incorporation of constrained cyclopropane-containing amino acid derivatives into peptide chains. The Fmoc group provides orthogonal protection, allowing selective deprotection under mild basic conditions while maintaining stability during solid-phase synthesis. Its rigid cyclopropyl structure influences peptide conformation, making it valuable in the design of peptidomimetics and bioactive molecules with enhanced metabolic stability and receptor selectivity. Commonly applied in medicinal chemistry for developing enzyme inhibitors and receptor modulators.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿30,320.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-(1-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)cyclopropyl)acetic acid
No image available

Used primarily in peptide synthesis as a protected amino acid building block, this compound enables the incorporation of constrained cyclopropane-containing amino acid derivatives into peptide chains. The Fmoc group provides orthogonal protection, allowing selective deprotection under mild basic conditions while maintaining stability during solid-phase synthesis. Its rigid cyclopropyl structure influences peptide conformation, making it valuable in the design of peptidomimetics and bioactive molecules wi

Used primarily in peptide synthesis as a protected amino acid building block, this compound enables the incorporation of constrained cyclopropane-containing amino acid derivatives into peptide chains. The Fmoc group provides orthogonal protection, allowing selective deprotection under mild basic conditions while maintaining stability during solid-phase synthesis. Its rigid cyclopropyl structure influences peptide conformation, making it valuable in the design of peptidomimetics and bioactive molecules with enhanced metabolic stability and receptor selectivity. Commonly applied in medicinal chemistry for developing enzyme inhibitors and receptor modulators.

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...