(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methyl-3-phenylpropanoic acid

≥95%

Reagent Code: #38019
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CAS Number 135944-05-7

science Other reagents with same CAS 135944-05-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 401.45 g/mol
Formula C₂₅H₂₃NO₄
badge Registry Numbers
MDL Number MFCD02682285
thermostat Physical Properties
Boiling Point 621.2°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily used in peptide synthesis, where it serves as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, ensuring selective reactions during the peptide chain assembly. It is particularly valuable in solid-phase peptide synthesis (SPPS), allowing for the stepwise construction of peptides with high precision. The compound’s structure, featuring a phenyl group and a methyl group, contributes to its stability and compatibility with various coupling reagents. After the peptide synthesis is complete, the Fmoc group can be easily removed under mild basic conditions, making it a versatile tool in the production of peptides for pharmaceutical and biochemical research.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to Off-White Solid
Purity (%) 95-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,401.00
inventory 100mg
10-20 days ฿1,008.00
inventory 5g
10-20 days ฿19,071.00
inventory 250mg
10-20 days ฿1,764.00

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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methyl-3-phenylpropanoic acid
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This chemical is primarily used in peptide synthesis, where it serves as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, ensuring selective reactions during the peptide chain assembly. It is particularly valuable in solid-phase peptide synthesis (SPPS), allowing for the stepwise construction of peptides with high precision. The compound’s structure, featuring a phenyl group and a methyl group, contributes to its stabilit

This chemical is primarily used in peptide synthesis, where it serves as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, ensuring selective reactions during the peptide chain assembly. It is particularly valuable in solid-phase peptide synthesis (SPPS), allowing for the stepwise construction of peptides with high precision. The compound’s structure, featuring a phenyl group and a methyl group, contributes to its stability and compatibility with various coupling reagents. After the peptide synthesis is complete, the Fmoc group can be easily removed under mild basic conditions, making it a versatile tool in the production of peptides for pharmaceutical and biochemical research.

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