(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-methoxy-5-oxopentanoic acid

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Reagent Code: #37431
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CAS Number 1481642-14-1

science Other reagents with same CAS 1481642-14-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 383.40 g/mol
Formula C₂₁H₂₁NO₆
badge Registry Numbers
MDL Number MFCD23381239
thermostat Physical Properties
Boiling Point 625.3°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily used in the field of peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amino functionality. This allows for selective deprotection during solid-phase peptide synthesis, enabling the stepwise assembly of peptide chains. The methoxy group on the pentanoic acid moiety provides additional stability and control during the synthesis process. Its application is crucial in the production of custom peptides for research, pharmaceuticals, and biotechnology, particularly in drug development and biochemical studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,040.00
inventory 250mg
10-20 days ฿2,511.00
inventory 5g
10-20 days ฿14,661.00

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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-methoxy-5-oxopentanoic acid
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This chemical is primarily used in the field of peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amino functionality. This allows for selective deprotection during solid-phase peptide synthesis, enabling the stepwise assembly of peptide chains. The methoxy group on the pentanoic acid moiety provides additional stability and control during the synthesis process

This chemical is primarily used in the field of peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amino functionality. This allows for selective deprotection during solid-phase peptide synthesis, enabling the stepwise assembly of peptide chains. The methoxy group on the pentanoic acid moiety provides additional stability and control during the synthesis process. Its application is crucial in the production of custom peptides for research, pharmaceuticals, and biotechnology, particularly in drug development and biochemical studies.

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