1-(4-Bromopyridin-2-yl)ethanone

97%

Reagent Code: #148429
fingerprint
CAS Number 1060805-69-7

science Other reagents with same CAS 1060805-69-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.03 g/mol
Formula C₇H₆BrNO
badge Registry Numbers
MDL Number MFCD13189212
thermostat Physical Properties
Boiling Point 267.3±25.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating pyridine-based drug candidates. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build complex heterocyclic systems. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its reactivity and stability in various transformation processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,810.00
inventory 250mg
10-20 days ฿2,660.00
inventory 1g
10-20 days ฿7,930.00
inventory 5g
10-20 days ฿31,680.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1-(4-Bromopyridin-2-yl)ethanone
No image available

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating pyridine-based drug candidates. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build complex heterocyclic systems. Also utilized in agrochemical research for designing novel pesticides

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating pyridine-based drug candidates. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build complex heterocyclic systems. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its reactivity and stability in various transformation processes.

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...