2-[(tert-Butoxycarbonyl)amino]pyridin-4-ylacetic acid

≥95%

Reagent Code: #149888
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CAS Number 887580-70-3

science Other reagents with same CAS 887580-70-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.27 g/mol
Formula C₁₂H₁₆N₂O₄
badge Registry Numbers
MDL Number MFCD07367939
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective modification in drug design, making it valuable in creating compounds with improved metabolic stability and binding affinity. Commonly employed in solid-phase and solution-phase peptide synthesis due to the presence of the Boc-protected amine group, which enables controlled deprotection and coupling steps. Also utilized in the preparation of pyridine-based heterocyclic systems for medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿7,280.00
inventory 50mg
10-20 days ฿21,740.00

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2-[(tert-Butoxycarbonyl)amino]pyridin-4-ylacetic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective modification in drug design, making it valuable in creating compounds with improved metabolic stability and binding affinity. Commonly employed in solid-phase and solution-phase peptide synthesis due to the presence of the Boc-protected amine group, which enables controlled deprotection and coupling steps.

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective modification in drug design, making it valuable in creating compounds with improved metabolic stability and binding affinity. Commonly employed in solid-phase and solution-phase peptide synthesis due to the presence of the Boc-protected amine group, which enables controlled deprotection and coupling steps. Also utilized in the preparation of pyridine-based heterocyclic systems for medicinal chemistry research.

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