(R)-2-(1-(((9H-Fluoren-9-yl)methoxy)carbonyl)piperidin-2-yl)acetic acid

97%

Reagent Code: #37275
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CAS Number 193693-63-9

science Other reagents with same CAS 193693-63-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 365.42 g/mol
Formula C₂₂H₂₃NO₄
badge Registry Numbers
MDL Number MFCD06656475
thermostat Physical Properties
Boiling Point 575.0±23.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is an Fmoc-protected (R)-(piperidin-2-yl)acetic acid widely used as a building block in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group protects the piperidine nitrogen, ensuring selective protection of the amine during the synthesis process and preventing unwanted reactions. Its application allows for the stepwise construction of peptides with high precision. After incorporation, the Fmoc group can be easily removed under mild basic conditions, making it a versatile tool in the production of complex peptides and proteins for pharmaceutical and biochemical research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,142.00
inventory 250mg
10-20 days ฿4,275.00

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(R)-2-(1-(((9H-Fluoren-9-yl)methoxy)carbonyl)piperidin-2-yl)acetic acid
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This compound is an Fmoc-protected (R)-(piperidin-2-yl)acetic acid widely used as a building block in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group protects the piperidine nitrogen, ensuring selective protection of the amine during the synthesis process and preventing unwanted reactions. Its application allows for the stepwise construction of peptides with high precision. After incorporation, the Fmoc group can be easily removed under m

This compound is an Fmoc-protected (R)-(piperidin-2-yl)acetic acid widely used as a building block in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group protects the piperidine nitrogen, ensuring selective protection of the amine during the synthesis process and preventing unwanted reactions. Its application allows for the stepwise construction of peptides with high precision. After incorporation, the Fmoc group can be easily removed under mild basic conditions, making it a versatile tool in the production of complex peptides and proteins for pharmaceutical and biochemical research.

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