(9H-fluoren-9-yl)methyl4-aminophenylcarbamate

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Reagent Code: #81897
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CAS Number 205688-13-7

science Other reagents with same CAS 205688-13-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 330.38 g/mol
Formula C₂₁H₁₈N₂O₂
badge Registry Numbers
MDL Number MFCD12912141
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, protected from light

description Product Description

Used primarily in organic synthesis, this compound serves as a protecting group for amines in peptide and nucleic acid chemistry. It is particularly valued for its stability under various reaction conditions, allowing for selective deprotection without affecting other functional groups. Additionally, it finds application in the development of fluorescent probes and markers due to its fluorenyl moiety, which exhibits strong fluorescence properties. This makes it useful in biochemical assays and imaging studies. Its role in solid-phase synthesis is also notable, where it aids in the stepwise construction of complex molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,731.00
inventory 1g
10-20 days ฿17,703.00

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(9H-fluoren-9-yl)methyl4-aminophenylcarbamate
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Used primarily in organic synthesis, this compound serves as a protecting group for amines in peptide and nucleic acid chemistry. It is particularly valued for its stability under various reaction conditions, allowing for selective deprotection without affecting other functional groups. Additionally, it finds application in the development of fluorescent probes and markers due to its fluorenyl moiety, which exhibits strong fluorescence properties. This makes it useful in biochemical assays and imaging st

Used primarily in organic synthesis, this compound serves as a protecting group for amines in peptide and nucleic acid chemistry. It is particularly valued for its stability under various reaction conditions, allowing for selective deprotection without affecting other functional groups. Additionally, it finds application in the development of fluorescent probes and markers due to its fluorenyl moiety, which exhibits strong fluorescence properties. This makes it useful in biochemical assays and imaging studies. Its role in solid-phase synthesis is also notable, where it aids in the stepwise construction of complex molecules.

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