2-bromo-3-methyl-5-nitropyridine

98%

Reagent Code: #148913
label
Alias 2-Bromo-5-nitro-3-methylpyridine; 2-Bromo-5-nitro-3-picoline
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CAS Number 23132-21-0

science Other reagents with same CAS 23132-21-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.02 g/mol
Formula C₆H₅BrN₂O₂
badge Registry Numbers
EC Number 677-832-1
MDL Number MFCD03095065
thermostat Physical Properties
Melting Point 55-59°C
Boiling Point 305.1°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.709±0.06 g/cm3
Storage 2-8℃, sealed, dry, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with potential antiviral and antibacterial properties. It serves as a building block in the preparation of more complex pyridine derivatives used in medicinal chemistry. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig amination to introduce functional groups for drug discovery research. Also utilized in agrochemical synthesis for creating novel pesticides and herbicides due to its reactive bromine site and electron-withdrawing nitro group, which facilitate further chemical modifications.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿770.00
inventory 25g
10-20 days ฿2,460.00

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2-bromo-3-methyl-5-nitropyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with potential antiviral and antibacterial properties. It serves as a building block in the preparation of more complex pyridine derivatives used in medicinal chemistry. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig amination to introduce functional groups for drug discovery research. Also utilized in agrochemical synthesis for creating novel pesticides and herbicides due to its reactive bromine site and electron-withdrawing nitro group, which facilitate further chemical modifications.
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