4-((3-Nitropyridin-2-yl)amino)butanoic acid

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Reagent Code: #219838
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CAS Number 339101-31-4

science Other reagents with same CAS 339101-31-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.21 g/mol
Formula C₉H₁₁N₃O₄
badge Registry Numbers
MDL Number MFCD00793101
inventory_2 Storage & Handling
Storage 2-8°C, drying away from light

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable heterocyclic structures that interact with biological targets. Also employed in research settings for designing new bioactive molecules with potential anti-inflammatory and antiviral properties. Its functional groups allow for easy modification, making it valuable in structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,750.00
inventory 250mg
10-20 days ฿4,550.00
inventory 1g
10-20 days ฿14,690.00

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4-((3-Nitropyridin-2-yl)amino)butanoic acid
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable heterocyclic structures that interact with biological targets. Also employed in research settings for designing new bioactive molecules with potential anti-inflammatory and antiviral properties. Its functional groups allow for easy modification, making it valuable in structure

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable heterocyclic structures that interact with biological targets. Also employed in research settings for designing new bioactive molecules with potential anti-inflammatory and antiviral properties. Its functional groups allow for easy modification, making it valuable in structure-activity relationship studies.

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