Allyl 2-((2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)ethyl)amino)acetate hydrochloride

97%

Reagent Code: #137051
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CAS Number 861114-47-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 416.90 g/mol
Formula C₂₂H₂₅ClN₂O₄
badge Registry Numbers
MDL Number MFCD28404628
inventory_2 Storage & Handling
Storage Store in inert gas at room temperature

description Product Description

Widely used in peptide synthesis, this compound serves as a protected amino acid building block, enabling stepwise assembly of peptides with high precision. The Fmoc group allows for mild base-induced deprotection, while the allyl ester offers orthogonal protection for the carboxylic acid, which can be selectively removed under neutral conditions using palladium catalysts. This makes it valuable in solid-phase peptide synthesis, especially when synthesizing complex peptides requiring selective side-chain deprotection. Its hydrochloride salt form enhances stability and solubility in common polar solvents, facilitating handling and coupling efficiency.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,000.00
inventory 1g
10-20 days ฿3,010.00
inventory 5g
10-20 days ฿12,110.00
Allyl 2-((2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)ethyl)amino)acetate hydrochloride
Widely used in peptide synthesis, this compound serves as a protected amino acid building block, enabling stepwise assembly of peptides with high precision. The Fmoc group allows for mild base-induced deprotection, while the allyl ester offers orthogonal protection for the carboxylic acid, which can be selectively removed under neutral conditions using palladium catalysts. This makes it valuable in solid-phase peptide synthesis, especially when synthesizing complex peptides requiring selective side-chain deprotection. Its hydrochloride salt form enhances stability and solubility in common polar solvents, facilitating handling and coupling efficiency.
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