4-Bromo-3-nitropyridine

95%

Reagent Code: #145064
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CAS Number 23056-44-2

science Other reagents with same CAS 23056-44-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.99 g/mol
Formula C₅H₃BrN₂O₂
badge Registry Numbers
MDL Number MFCD04112576
thermostat Physical Properties
Boiling Point 239.9°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where the bromo and nitro functional groups allow for further chemical modifications. Its structure supports cross-coupling reactions, making it valuable in the preparation of more complex heterocyclic compounds. Commonly employed in research and development for agrochemicals and medicinal chemistry due to its reactivity and ability to serve as a building block in multi-step organic syntheses.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,770.00
inventory 250mg
10-20 days ฿6,400.00

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4-Bromo-3-nitropyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where the bromo and nitro functional groups allow for further chemical modifications. Its structure supports cross-coupling reactions, making it valuable in the preparation of more complex heterocyclic compounds. Commonly employed in research and development for agrochemicals and medicinal chemistry due to its reactivity and ability to serve as a building block in multi

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where the bromo and nitro functional groups allow for further chemical modifications. Its structure supports cross-coupling reactions, making it valuable in the preparation of more complex heterocyclic compounds. Commonly employed in research and development for agrochemicals and medicinal chemistry due to its reactivity and ability to serve as a building block in multi-step organic syntheses.

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