(9H-Fluoren-9-yl)methyl (2-(2-(2-aminoethoxy)ethoxy)ethyl)carbamate hydrochloride

95%

Reagent Code: #87126
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CAS Number 868599-73-9

science Other reagents with same CAS 868599-73-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 406.90 g/mol
Formula C₂₁H₂₇ClN₂O₄
badge Registry Numbers
MDL Number MFCD04112696
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily utilized in the field of peptide synthesis and organic chemistry as a protecting group for amines. Its fluorenylmethyloxycarbonyl (Fmoc) group is particularly effective in safeguarding amino groups during the synthesis of peptides, ensuring that specific reactions occur at desired sites without interference. The hydrophilic chain in its structure enhances solubility in aqueous solutions, making it suitable for use in various biochemical and bioconjugation applications. Additionally, it is employed in the development of drug delivery systems and as a linker in solid-phase synthesis, facilitating the creation of complex molecules with precision. Its hydrochloride form ensures stability and ease of handling in laboratory settings.

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Test Parameter Specification
Appearance White to Off-white 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 ฿23,382.00
inventory 250mg
10-20 days ฿3,024.00
inventory 1g
10-20 days ฿6,048.00

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(9H-Fluoren-9-yl)methyl (2-(2-(2-aminoethoxy)ethoxy)ethyl)carbamate hydrochloride
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This chemical is primarily utilized in the field of peptide synthesis and organic chemistry as a protecting group for amines. Its fluorenylmethyloxycarbonyl (Fmoc) group is particularly effective in safeguarding amino groups during the synthesis of peptides, ensuring that specific reactions occur at desired sites without interference. The hydrophilic chain in its structure enhances solubility in aqueous solutions, making it suitable for use in various biochemical and bioconjugation applications. Addition

This chemical is primarily utilized in the field of peptide synthesis and organic chemistry as a protecting group for amines. Its fluorenylmethyloxycarbonyl (Fmoc) group is particularly effective in safeguarding amino groups during the synthesis of peptides, ensuring that specific reactions occur at desired sites without interference. The hydrophilic chain in its structure enhances solubility in aqueous solutions, making it suitable for use in various biochemical and bioconjugation applications. Additionally, it is employed in the development of drug delivery systems and as a linker in solid-phase synthesis, facilitating the creation of complex molecules with precision. Its hydrochloride form ensures stability and ease of handling in laboratory settings.

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