Fmoc-D-alaninol

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Reagent Code: #53653
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CAS Number 202751-95-9

science Other reagents with same CAS 202751-95-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.35 g/mol
Formula C₁₈H₁₉NO₃
badge Registry Numbers
MDL Number MFCD00270234
thermostat Physical Properties
Boiling Point 503.9°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

Fmoc-D-alaninol is a protected derivative of D-alaninol, featuring the Fmoc (9-fluorenylmethyloxycarbonyl) protecting group on the amino functionality. It serves as a key building block in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), where it enables the incorporation of a reduced amino acid residue or hydroxyalkylamine moiety into peptide chains. The Fmoc group facilitates orthogonal protection strategies, allowing precise stepwise assembly of peptides while preventing unwanted side reactions. This compound is vital in pharmaceutical research for synthesizing peptide-based drugs, peptidomimetics, and bioactive molecules, as well as in biochemical studies exploring protein structures, enzyme mechanisms, and novel therapeutic agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿9,513.00
inventory 10g
10-20 days ฿18,261.00
inventory 1g
10-20 days ฿2,385.00
inventory 250mg
10-20 days ฿945.00

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Fmoc-D-alaninol
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Fmoc-D-alaninol is a protected derivative of D-alaninol, featuring the Fmoc (9-fluorenylmethyloxycarbonyl) protecting group on the amino functionality. It serves as a key building block in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), where it enables the incorporation of a reduced amino acid residue or hydroxyalkylamine moiety into peptide chains. The Fmoc group facilitates orthogonal protection strategies, allowing precise stepwise assembly of peptides while preventing unwant

Fmoc-D-alaninol is a protected derivative of D-alaninol, featuring the Fmoc (9-fluorenylmethyloxycarbonyl) protecting group on the amino functionality. It serves as a key building block in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), where it enables the incorporation of a reduced amino acid residue or hydroxyalkylamine moiety into peptide chains. The Fmoc group facilitates orthogonal protection strategies, allowing precise stepwise assembly of peptides while preventing unwanted side reactions. This compound is vital in pharmaceutical research for synthesizing peptide-based drugs, peptidomimetics, and bioactive molecules, as well as in biochemical studies exploring protein structures, enzyme mechanisms, and novel therapeutic agents.

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