2-bromo-3-methyl-5-nitropyridine

≥95%

Reagent Code: #144190
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, dried, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) targeting central nervous system disorders and anti-inflammatory agents. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in agrochemical research for developing novel pesticides and herbicides due to its electron-deficient pyridine core. Preferred in medicinal chemistry for its ability to enhance binding affinity and metabolic stability in lead compounds.

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Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿1,390.00

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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) targeting central nervous system disorders and anti-inflammatory agents. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in agrochemical research for developi

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) targeting central nervous system disorders and anti-inflammatory agents. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in agrochemical research for developing novel pesticides and herbicides due to its electron-deficient pyridine core. Preferred in medicinal chemistry for its ability to enhance binding affinity and metabolic stability in lead compounds.

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