2-Bromo-4-ethoxymethyl-pyridine

97%

Reagent Code: #152246
fingerprint
CAS Number 1289385-06-3

science Other reagents with same CAS 1289385-06-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.075 g/mol
Formula C₈H₁₀BrNO
badge Registry Numbers
MDL Number MFCD18837158
thermostat Physical Properties
Boiling Point 268 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.398 g/cm3
Storage Room temperature, seal, dry

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 inflammation. Its structure allows for selective functionalization, making it valuable in creating complex pyridine-based drug molecules. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build biaryl systems in medicinal chemistry. Also utilized in agrochemical research for developing novel pesticides and herbicides due to its stability and reactivity profile.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿28,770.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-Bromo-4-ethoxymethyl-pyridine
No image available

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) targeting central nervous system disorders and inflammation. Its structure allows for selective functionalization, making it valuable in creating complex pyridine-based drug molecules. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build biaryl systems in medicinal chemistry. Also utilized in agrochemical research for developing novel

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) targeting central nervous system disorders and inflammation. Its structure allows for selective functionalization, making it valuable in creating complex pyridine-based drug molecules. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build biaryl systems in medicinal chemistry. Also utilized in agrochemical research for developing novel pesticides and herbicides due to its stability and reactivity profile.

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...