6-((tert-Butoxycarbonyl)amino)-2-fluoronicotinic acid

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Reagent Code: #150808
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CAS Number 1445962-38-8

science Other reagents with same CAS 1445962-38-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 256.23 g/mol
Formula C₁₁H₁₃FN₂O₄
thermostat Physical Properties
Boiling Point 351.8±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.359±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antiviral agents. Its structure supports the construction of complex heterocyclic systems found in bioactive molecules. The Boc-protected amine and carboxylic acid functionalities allow for selective and sequential coupling reactions, making it valuable in solid-phase and solution-phase peptide-like synthesis. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate electronic and steric properties in drug candidates.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,830.00
inventory 250mg
10-20 days ฿21,420.00
inventory 1g
10-20 days ฿51,580.00

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6-((tert-Butoxycarbonyl)amino)-2-fluoronicotinic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antiviral agents. Its structure supports the construction of complex heterocyclic systems found in bioactive molecules. The Boc-protected amine and carboxylic acid functionalities allow for selective and sequential coupling reactions, making it valuable in solid-phase and solution-phase peptide-like synthesis. Commonly employed in medicinal chemistry for structure-activity rel

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antiviral agents. Its structure supports the construction of complex heterocyclic systems found in bioactive molecules. The Boc-protected amine and carboxylic acid functionalities allow for selective and sequential coupling reactions, making it valuable in solid-phase and solution-phase peptide-like synthesis. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate electronic and steric properties in drug candidates.

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