Allyl 2-((2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)ethyl)amino)acetate hydrochloride
97%
Reagent
Code: #137051
CAS Number
861114-47-8
blur_circular Chemical Specifications
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Molecular Information
Weight
416.90 g/mol
Formula
C₂₂H₂₅ClN₂O₄
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Registry Numbers
MDL Number
MFCD28404628
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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.
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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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