(R)-3-tert-Butoxycarbonylamino-3-(3-fluorophenyl)propionic acid

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Reagent Code: #104644
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CAS Number 500789-04-8

science Other reagents with same CAS 500789-04-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 283.30 g/mol
Formula C₁₄H₁₈FNO₄
badge Registry Numbers
MDL Number MFCD03427956
thermostat Physical Properties
Boiling Point 422.1°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a fluorophenyl group and a tert-butoxycarbonyl (Boc) protected amine, makes it valuable in the development of peptide-based drugs and small molecule inhibitors. The fluorine atom enhances the metabolic stability and binding affinity of the final compounds, while the Boc group provides protection during synthetic processes, ensuring selective reactions. It is particularly relevant in the production of drugs targeting neurological disorders, cancer, and inflammation, where precise molecular interactions are critical. The compound’s chiral center also allows for the creation of enantiomerically pure substances, which is essential for optimizing therapeutic efficacy and reducing side effects.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,259.00
inventory 1g
10-20 days ฿4,707.00
inventory 5g
10-20 days ฿23,490.00

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(R)-3-tert-Butoxycarbonylamino-3-(3-fluorophenyl)propionic acid
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This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a fluorophenyl group and a tert-butoxycarbonyl (Boc) protected amine, makes it valuable in the development of peptide-based drugs and small molecule inhibitors. The fluorine atom enhances the metabolic stability and binding affinity of the final compounds, while the Boc group provides protection during synthetic processes, ensuring se

This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a fluorophenyl group and a tert-butoxycarbonyl (Boc) protected amine, makes it valuable in the development of peptide-based drugs and small molecule inhibitors. The fluorine atom enhances the metabolic stability and binding affinity of the final compounds, while the Boc group provides protection during synthetic processes, ensuring selective reactions. It is particularly relevant in the production of drugs targeting neurological disorders, cancer, and inflammation, where precise molecular interactions are critical. The compound’s chiral center also allows for the creation of enantiomerically pure substances, which is essential for optimizing therapeutic efficacy and reducing side effects.

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