3-nitropyridine-2-carbaldehyde

≥95%

Reagent Code: #216908
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CAS Number 10261-94-6

science Other reagents with same CAS 10261-94-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 152.11 g/mol
Formula C₆H₄N₂O₃
badge Registry Numbers
MDL Number MFCD10696871
inventory_2 Storage & Handling
Density 1.432±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor ligands and other biologically active compounds. It serves as a building block in organic synthesis for constructing nitrogen-containing heterocycles. Its aldehyde and nitro functional groups allow for diverse chemical transformations, such as reduction, condensation, and cyclization reactions. Commonly employed in the preparation of pyridine-based drugs and agrochemicals due to its reactivity and structural features. Also utilized in research settings for developing fluorescent probes and sensors owing to its electron-withdrawing properties and ability to form Schiff bases.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,810.00
inventory 250mg
10-20 days ฿4,150.00
inventory 1g
10-20 days ฿6,540.00
inventory 5g
10-20 days ฿26,660.00
inventory 25g
10-20 days ฿93,320.00

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3-nitropyridine-2-carbaldehyde
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor ligands and other biologically active compounds. It serves as a building block in organic synthesis for constructing nitrogen-containing heterocycles. Its aldehyde and nitro functional groups allow for diverse chemical transformations, such as reduction, condensation, and cyclization reactions. Commonly employed in the preparation of pyridine-based drugs and agrochemicals due to its reactivi

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor ligands and other biologically active compounds. It serves as a building block in organic synthesis for constructing nitrogen-containing heterocycles. Its aldehyde and nitro functional groups allow for diverse chemical transformations, such as reduction, condensation, and cyclization reactions. Commonly employed in the preparation of pyridine-based drugs and agrochemicals due to its reactivity and structural features. Also utilized in research settings for developing fluorescent probes and sensors owing to its electron-withdrawing properties and ability to form Schiff bases.

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