3-(5-Nitropyridin-2-yl)benzoic acid

95%

Reagent Code: #217301
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CAS Number 864075-95-6

science Other reagents with same CAS 864075-95-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.2 g/mol
Formula C₁₂H₈N₂O₄
badge Registry Numbers
MDL Number MFCD05864815
thermostat Physical Properties
Boiling Point 477.3°C
inventory_2 Storage & Handling
Storage Room temperature, dry

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 enhance binding affinity to target proteins. Also employed in the preparation of agrochemicals and functional materials where nitro-aromatic systems contribute to electronic or photochemical properties. Its carboxylic acid group allows for easy derivatization, enabling conjugation into larger molecules for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,260.00
inventory 1g
10-20 days ฿8,100.00

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3-(5-Nitropyridin-2-yl)benzoic 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 enhance binding affinity to target proteins. Also employed in the preparation of agrochemicals and functional materials where nitro-aromatic systems contribute to electronic or photochemical properties. Its carboxylic acid group allows for easy der

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 enhance binding affinity to target proteins. Also employed in the preparation of agrochemicals and functional materials where nitro-aromatic systems contribute to electronic or photochemical properties. Its carboxylic acid group allows for easy derivatization, enabling conjugation into larger molecules for structure-activity relationship studies.

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