2-Chloro-5-nitroisonicotinaldehyde

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Reagent Code: #131278
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CAS Number 946136-72-7

science Other reagents with same CAS 946136-72-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.55 g/mol
Formula C₆H₃ClN₂O₃
badge Registry Numbers
MDL Number MFCD11977455
thermostat Physical Properties
Boiling Point 336.2±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.579±0.06 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization, making it valuable in constructing nitrogen-containing heterocyclic compounds. Commonly employed in the development of kinase inhibitors and other biologically active molecules. Also utilized in the preparation of dyes and fluorescent probes due to its electron-withdrawing substituents and aldehyde reactivity. Suitable for use in condensation reactions and as a building block in combinatorial chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,400.00
inventory 250mg
10-20 days ฿12,710.00

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2-Chloro-5-nitroisonicotinaldehyde
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization, making it valuable in constructing nitrogen-containing heterocyclic compounds. Commonly employed in the development of kinase inhibitors and other biologically active molecules. Also utilized in the preparation of dyes and fluorescent probes due to its electron-withdrawing substituents and aldehyde reactivity. Suitable for use in condensation reactions and as a bu

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization, making it valuable in constructing nitrogen-containing heterocyclic compounds. Commonly employed in the development of kinase inhibitors and other biologically active molecules. Also utilized in the preparation of dyes and fluorescent probes due to its electron-withdrawing substituents and aldehyde reactivity. Suitable for use in condensation reactions and as a building block in combinatorial chemistry.

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