2-(((((9H-fluorene-9-yl) methoxy) carbonyl) (2,4-dimethoxybenzyl) amino) acetic acid

97%

Reagent Code: #41090
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CAS Number 166881-42-1

science Other reagents with same CAS 166881-42-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 447.48 g/mol
Formula C₂₆H₂₅NO₆
badge Registry Numbers
MDL Number MFCD08064316
thermostat Physical Properties
Boiling Point 653.2 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.280±0.06 g/cm3
Storage 2-8℃, inert gas

description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly in peptide chemistry, where it serves as a protecting group for amino acids during the synthesis of peptides. The fluorenylmethoxycarbonyl (Fmoc) group, a component of this compound, is widely used due to its stability under basic conditions and ease of removal under mild acidic conditions. This makes it highly effective in solid-phase peptide synthesis (SPPS), allowing for the stepwise construction of peptides with high precision and yield. Additionally, the 2,4-dimethoxybenzyl group provides further protection for specific functional groups, enhancing the selectivity and efficiency of the synthesis process. Its application is critical in the production of complex peptides for pharmaceutical research, drug development, and biochemical studies.

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Test Parameter Specification
Appearance White to off-white solid
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿6,710.00
inventory 5g
10-20 days ฿23,680.00
inventory 250mg
10-20 days ฿2,880.00

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2-(((((9H-fluorene-9-yl) methoxy) carbonyl) (2,4-dimethoxybenzyl) amino) acetic acid
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This chemical is primarily utilized in the field of organic synthesis, particularly in peptide chemistry, where it serves as a protecting group for amino acids during the synthesis of peptides. The fluorenylmethoxycarbonyl (Fmoc) group, a component of this compound, is widely used due to its stability under basic conditions and ease of removal under mild acidic conditions. This makes it highly effective in solid-phase peptide synthesis (SPPS), allowing for the stepwise construction of peptides with high

This chemical is primarily utilized in the field of organic synthesis, particularly in peptide chemistry, where it serves as a protecting group for amino acids during the synthesis of peptides. The fluorenylmethoxycarbonyl (Fmoc) group, a component of this compound, is widely used due to its stability under basic conditions and ease of removal under mild acidic conditions. This makes it highly effective in solid-phase peptide synthesis (SPPS), allowing for the stepwise construction of peptides with high precision and yield. Additionally, the 2,4-dimethoxybenzyl group provides further protection for specific functional groups, enhancing the selectivity and efficiency of the synthesis process. Its application is critical in the production of complex peptides for pharmaceutical research, drug development, and biochemical studies.

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