2-(7-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-oxo-2H-chromen-4-yl)acetic acid

≥95%

Reagent Code: #113385
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CAS Number 378247-75-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 441.43 g/mol
Formula C₂₆H₁₉NO₆
badge Registry Numbers
MDL Number MFCD13195295
thermostat Physical Properties
Boiling Point 660.549°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily used in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group, which is part of its structure, is widely employed in solid-phase peptide synthesis to protect the amino group during the coupling process. The coumarin moiety in the structure can also be utilized for fluorescent labeling, making it useful in biochemical assays and imaging studies. Additionally, its unique structure allows for applications in the development of photolabile protecting groups, which can be cleaved upon exposure to light, enabling controlled release in various chemical and biological processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days €155.40
inventory 250mg
10-20 days €310.56
2-(7-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-oxo-2H-chromen-4-yl)acetic acid
This chemical is primarily used in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group, which is part of its structure, is widely employed in solid-phase peptide synthesis to protect the amino group during the coupling process. The coumarin moiety in the structure can also be utilized for fluorescent labeling, making it useful in biochemical assays and imaging studies. Additionally, its unique structure allows for applications in the development of photolabile protecting groups, which can be cleaved upon exposure to light, enabling controlled release in various chemical and biological processes.
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