(9H-Fluoren-9-yl)methyl 4-aminobenzylcarbamate

95%

Reagent Code: #104164
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CAS Number 159790-81-5

science Other reagents with same CAS 159790-81-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 344.41 g/mol
Formula C₂₂H₂₀N₂O₂
badge Registry Numbers
MDL Number MFCD06658452
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used in peptide synthesis as a protecting group for amines. It helps prevent unwanted reactions during the synthesis process, ensuring the correct sequence of amino acids in the peptide chain. The fluorenylmethyloxycarbonyl (Fmoc) group, which is part of this compound, is particularly valued for its stability under basic conditions and its ease of removal under mild acidic conditions. This makes it a preferred choice in solid-phase peptide synthesis, where it allows for the stepwise construction of peptides with high precision. Additionally, it is used in the synthesis of various organic compounds where selective protection of amine groups is required.

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Test Parameter Specification
Appearance White to Light Brown Solid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿8,730.00
inventory 250mg
10-20 days ฿1,170.00
inventory 1g
10-20 days ฿2,637.00

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(9H-Fluoren-9-yl)methyl 4-aminobenzylcarbamate
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This chemical is primarily used in peptide synthesis as a protecting group for amines. It helps prevent unwanted reactions during the synthesis process, ensuring the correct sequence of amino acids in the peptide chain. The fluorenylmethyloxycarbonyl (Fmoc) group, which is part of this compound, is particularly valued for its stability under basic conditions and its ease of removal under mild acidic conditions. This makes it a preferred choice in solid-phase peptide synthesis, where it allows for the ste

This chemical is primarily used in peptide synthesis as a protecting group for amines. It helps prevent unwanted reactions during the synthesis process, ensuring the correct sequence of amino acids in the peptide chain. The fluorenylmethyloxycarbonyl (Fmoc) group, which is part of this compound, is particularly valued for its stability under basic conditions and its ease of removal under mild acidic conditions. This makes it a preferred choice in solid-phase peptide synthesis, where it allows for the stepwise construction of peptides with high precision. Additionally, it is used in the synthesis of various organic compounds where selective protection of amine groups is required.

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