4-Bromo-1-methylpyridin-2(1H)-one

98%

Reagent Code: #145116
fingerprint
CAS Number 214342-63-9

science Other reagents with same CAS 214342-63-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.02 g/mol
Formula C₆H₆BrNO
badge Registry Numbers
MDL Number MFCD11226870
thermostat Physical Properties
Boiling Point 258°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in the preparation of agrochemicals and functional materials where brominated pyridine derivatives serve as key building blocks.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿154.00
inventory 1g
10-20 days ฿176.00
inventory 25g
10-20 days ฿5,260.00
inventory 100g
10-20 days ฿17,910.00
inventory 5g
10-20 days ฿1,390.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-Bromo-1-methylpyridin-2(1H)-one
No image available

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in the preparation of agrochemicals and functional materials where bro

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in the preparation of agrochemicals and functional materials where brominated pyridine derivatives serve as key building blocks.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...