Boc-Ser(Ala-Fmoc)-OH

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Reagent Code: #64975
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CAS Number 944283-07-2

science Other reagents with same CAS 944283-07-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 498.53 g/mol
Formula C₂₆H₃₀N₂O₈
badge Registry Numbers
MDL Number MFCD10001363
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This chemical is a specialized building block in peptide synthesis, specifically N-Boc-O-(N-Fmoc-L-alanyl)-L-serine. The Boc (tert-butyloxycarbonyl) group protects the α-amine of serine, while the side chain hydroxyl of serine is protected via an ester linkage to N-Fmoc-alanine. This dual protection strategy, incorporating an Fmoc-protected alanine residue on the serine side chain, enables selective deprotection and orthogonal protection schemes during stepwise peptide assembly. It is essential in solid-phase peptide synthesis (SPPS) for constructing complex peptides with precise sequence control and high purity. Applications include pharmaceutical research, biotechnology, and the development of therapeutic peptides and peptidomimetics.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,221.00

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Boc-Ser(Ala-Fmoc)-OH
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This chemical is a specialized building block in peptide synthesis, specifically N-Boc-O-(N-Fmoc-L-alanyl)-L-serine. The Boc (tert-butyloxycarbonyl) group protects the α-amine of serine, while the side chain hydroxyl of serine is protected via an ester linkage to N-Fmoc-alanine. This dual protection strategy, incorporating an Fmoc-protected alanine residue on the serine side chain, enables selective deprotection and orthogonal protection schemes during stepwise peptide assembly. It is essential in solid-

This chemical is a specialized building block in peptide synthesis, specifically N-Boc-O-(N-Fmoc-L-alanyl)-L-serine. The Boc (tert-butyloxycarbonyl) group protects the α-amine of serine, while the side chain hydroxyl of serine is protected via an ester linkage to N-Fmoc-alanine. This dual protection strategy, incorporating an Fmoc-protected alanine residue on the serine side chain, enables selective deprotection and orthogonal protection schemes during stepwise peptide assembly. It is essential in solid-phase peptide synthesis (SPPS) for constructing complex peptides with precise sequence control and high purity. Applications include pharmaceutical research, biotechnology, and the development of therapeutic peptides and peptidomimetics.

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