2-(Chloromethyl)-4-nitropyridine

95%

Reagent Code: #163770
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CAS Number 312321-71-4

science Other reagents with same CAS 312321-71-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.57 g/mol
Formula C₆H₅ClN₂O₂
badge Registry Numbers
MDL Number MFCD07368191
thermostat Physical Properties
Boiling Point 305.6±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.412±0.06 g/cm3(Predicted)
Storage -20°C, Inert Gas

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of pyridine-based drugs. Its reactive chloromethyl group allows for easy attachment to other molecules, making it valuable in constructing complex organic compounds. Commonly employed in the preparation of kinase inhibitors and other bioactive agents. Also utilized in agrochemical synthesis for creating novel pesticide candidates. The nitro group enhances reactivity and can be reduced to an amine for further functionalization in multi-step reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,510.00
inventory 1g
10-20 days ฿36,580.00
inventory 250mg
10-20 days ฿11,050.00

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2-(Chloromethyl)-4-nitropyridine
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Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of pyridine-based drugs. Its reactive chloromethyl group allows for easy attachment to other molecules, making it valuable in constructing complex organic compounds. Commonly employed in the preparation of kinase inhibitors and other bioactive agents. Also utilized in agrochemical synthesis for creating novel pesticide candidates. The nitro group enhances reactivity and can be reduced to an amine for fu

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of pyridine-based drugs. Its reactive chloromethyl group allows for easy attachment to other molecules, making it valuable in constructing complex organic compounds. Commonly employed in the preparation of kinase inhibitors and other bioactive agents. Also utilized in agrochemical synthesis for creating novel pesticide candidates. The nitro group enhances reactivity and can be reduced to an amine for further functionalization in multi-step reactions.

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