(9H-Fluoren-9-yl)methyl (6-hydroxyhexyl)carbamate

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Reagent Code: #104165
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CAS Number 127903-20-2

science Other reagents with same CAS 127903-20-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 339.43 g/mol
Formula C₂₁H₂₅NO₃
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MDL Number MFCD00380196
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used in the field of organic synthesis and peptide chemistry. It serves as a protecting group for amines during complex chemical reactions, particularly in the synthesis of peptides and other biomolecules. The fluorenylmethyloxycarbonyl (Fmoc) group, which is part of this compound, is widely employed in solid-phase peptide synthesis (SPPS) due to its stability under various reaction conditions and its ability to be selectively removed under mild basic conditions. This makes it highly valuable in the production of peptides for pharmaceutical research, drug development, and biochemical studies. Additionally, its hydroxyhexyl moiety can enhance solubility in organic solvents, facilitating its use in diverse synthetic applications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿882.00
inventory 250mg
10-20 days ฿441.00
inventory 5g
10-20 days ฿4,365.00

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(9H-Fluoren-9-yl)methyl (6-hydroxyhexyl)carbamate
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This chemical is primarily used in the field of organic synthesis and peptide chemistry. It serves as a protecting group for amines during complex chemical reactions, particularly in the synthesis of peptides and other biomolecules. The fluorenylmethyloxycarbonyl (Fmoc) group, which is part of this compound, is widely employed in solid-phase peptide synthesis (SPPS) due to its stability under various reaction conditions and its ability to be selectively removed under mild basic conditions. This makes it

This chemical is primarily used in the field of organic synthesis and peptide chemistry. It serves as a protecting group for amines during complex chemical reactions, particularly in the synthesis of peptides and other biomolecules. The fluorenylmethyloxycarbonyl (Fmoc) group, which is part of this compound, is widely employed in solid-phase peptide synthesis (SPPS) due to its stability under various reaction conditions and its ability to be selectively removed under mild basic conditions. This makes it highly valuable in the production of peptides for pharmaceutical research, drug development, and biochemical studies. Additionally, its hydroxyhexyl moiety can enhance solubility in organic solvents, facilitating its use in diverse synthetic applications.

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