(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-hydroxy-3-methylbutanoic acid

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Reagent Code: #37755
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CAS Number 884880-39-1

science Other reagents with same CAS 884880-39-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 355.38 g/mol
Formula C₂₀H₂₁NO₅
badge Registry Numbers
MDL Number MFCD02682577
thermostat Physical Properties
Boiling Point 595.5±50.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily used in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group protects the amino group during the synthesis process, allowing selective reactions to occur at other functional groups. The hydroxyl and carboxyl groups in the molecule can also be utilized for further chemical modifications or conjugation. Its application is particularly significant in solid-phase peptide synthesis (SPPS), where it ensures the stepwise assembly of peptides with high precision. Additionally, its chiral nature makes it valuable in the synthesis of enantiomerically pure compounds, which are essential in pharmaceutical research and development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,005.00
inventory 250mg
10-20 days ฿8,001.00

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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-hydroxy-3-methylbutanoic acid
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This compound is primarily used in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group protects the amino group during the synthesis process, allowing selective reactions to occur at other functional groups. The hydroxyl and carboxyl groups in the molecule can also be utilized for further chemical modifications or conjugation. Its application is particularly significant in solid-phase peptide synthesis (SPPS), where it ensures the stepwise assembly of peptid

This compound is primarily used in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group protects the amino group during the synthesis process, allowing selective reactions to occur at other functional groups. The hydroxyl and carboxyl groups in the molecule can also be utilized for further chemical modifications or conjugation. Its application is particularly significant in solid-phase peptide synthesis (SPPS), where it ensures the stepwise assembly of peptides with high precision. Additionally, its chiral nature makes it valuable in the synthesis of enantiomerically pure compounds, which are essential in pharmaceutical research and development.

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