N-Fmoc-L-threonol

98%

Reagent Code: #216626
label
Alias 2-(N-Fmoc)-amino-1,3-butanediol;N-alpha-(9-fluorene methoxycarbonyl)-L-threminol
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CAS Number 176380-53-3

science Other reagents with same CAS 176380-53-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 327.5 g/mol
Formula C₁₉H₂₁NO₄
badge Registry Numbers
MDL Number MFCD00270218
inventory_2 Storage & Handling
Storage -20°C

description Product Description

N-Fmoc-L-threoninol is employed in solid-phase peptide synthesis as a protected amino alcohol building block, facilitating selective incorporation at the C-terminus or as a spacer in peptide chains. The Fmoc protecting group permits mild base-mediated deprotection, ensuring compatibility with diverse orthogonal side-chain protecting strategies. Renowned for its stability and preservation of stereochemical integrity, it is widely used in the assembly of complex peptides, glycopeptides, and peptide conjugates. Essential in the production of peptide-based pharmaceuticals, biochemical probes, and advanced research tools demanding precise structural modulation.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿850.00
N-Fmoc-L-threonol
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N-Fmoc-L-threoninol is employed in solid-phase peptide synthesis as a protected amino alcohol building block, facilitating selective incorporation at the C-terminus or as a spacer in peptide chains. The Fmoc protecting group permits mild base-mediated deprotection, ensuring compatibility with diverse orthogonal side-chain protecting strategies. Renowned for its stability and preservation of stereochemical integrity, it is widely used in the assembly of complex peptides, glycopeptides, and peptide conjuga

N-Fmoc-L-threoninol is employed in solid-phase peptide synthesis as a protected amino alcohol building block, facilitating selective incorporation at the C-terminus or as a spacer in peptide chains. The Fmoc protecting group permits mild base-mediated deprotection, ensuring compatibility with diverse orthogonal side-chain protecting strategies. Renowned for its stability and preservation of stereochemical integrity, it is widely used in the assembly of complex peptides, glycopeptides, and peptide conjugates. Essential in the production of peptide-based pharmaceuticals, biochemical probes, and advanced research tools demanding precise structural modulation.

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