2-((tert-Butoxycarbonyl)amino)-2-(2-fluorophenyl)acetic acid

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Reagent Code: #41172
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CAS Number 161330-30-9

science Other reagents with same CAS 161330-30-9

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scatter_plot Molecular Information
Weight 269.2689 g/mol
Formula C₁₃H₁₆FNO₄
badge Registry Numbers
MDL Number MFCD02682469
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description Product Description

This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of peptide-based drugs. It serves as a key intermediate in the production of active pharmaceutical ingredients (APIs) that target specific biological pathways. Its structure, featuring a fluorophenyl group and a Boc-protected amino group, makes it valuable for introducing fluorine atoms into peptides, enhancing their stability and bioavailability. Additionally, it is employed in the creation of custom peptides for drug discovery, enabling the study of receptor-ligand interactions and the development of targeted therapies for various diseases, including cancer and neurological disorders.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,674.00
inventory 250mg
10-20 days ฿1,620.00
inventory 1g
10-20 days ฿5,590.00
inventory 10g
10-20 days ฿34,200.00

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2-((tert-Butoxycarbonyl)amino)-2-(2-fluorophenyl)acetic acid
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This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of peptide-based drugs. It serves as a key intermediate in the production of active pharmaceutical ingredients (APIs) that target specific biological pathways. Its structure, featuring a fluorophenyl group and a Boc-protected amino group, makes it valuable for introducing fluorine atoms into peptides, enhancing their stability and bioavailability. Additionally, it is employed in the

This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of peptide-based drugs. It serves as a key intermediate in the production of active pharmaceutical ingredients (APIs) that target specific biological pathways. Its structure, featuring a fluorophenyl group and a Boc-protected amino group, makes it valuable for introducing fluorine atoms into peptides, enhancing their stability and bioavailability. Additionally, it is employed in the creation of custom peptides for drug discovery, enabling the study of receptor-ligand interactions and the development of targeted therapies for various diseases, including cancer and neurological disorders.

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