2-(7-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-oxo-2H-chromen-4-yl)acetic acid
≥95%
Reagent
Code: #113385
CAS Number
378247-75-7
blur_circular Chemical Specifications
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Molecular Information
Weight
441.43 g/mol
Formula
C₂₆H₁₉NO₆
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Registry Numbers
MDL Number
MFCD13195295
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Physical Properties
Boiling Point
660.549°C at 760 mmHg
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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.
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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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