4-Bromo-2,5-dimethylpyridine

95%

Reagent Code: #146785
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CAS Number 17117-23-6

science Other reagents with same CAS 17117-23-6

blur_circular Chemical Specifications

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Weight 186.05 g/mol
Formula C₇H₈BrN
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 pyridine ring serves as a core structure. Its bromine substituent at the 4-position allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, making it valuable in medicinal chemistry for building complex molecules. Also employed in the production of agrochemicals and specialty chemicals requiring substituted pyridine derivatives. The methyl groups at the 2- and 5-positions enhance electron density on the pyridine ring, influencing reactivity and selectivity in synthetic pathways.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,200.00
inventory 250mg
10-20 days ฿5,600.00
inventory 1g
10-20 days ฿16,000.00
inventory 5g
10-20 days ฿44,800.00

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4-Bromo-2,5-dimethylpyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where the pyridine ring serves as a core structure. Its bromine substituent at the 4-position allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, making it valuable in medicinal chemistry for building complex molecules. Also employed in the production of agrochemicals and specialty chemicals requiring substituted pyridine

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where the pyridine ring serves as a core structure. Its bromine substituent at the 4-position allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, making it valuable in medicinal chemistry for building complex molecules. Also employed in the production of agrochemicals and specialty chemicals requiring substituted pyridine derivatives. The methyl groups at the 2- and 5-positions enhance electron density on the pyridine ring, influencing reactivity and selectivity in synthetic pathways.

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