3-Bromo-5-phenoxypyridine

95%

Reagent Code: #150446
fingerprint
CAS Number 28232-63-5

science Other reagents with same CAS 28232-63-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.09 g/mol
Formula C₁₁H₈BrNO
badge Registry Numbers
MDL Number MFCD10698710
thermostat Physical Properties
Boiling Point 311.6±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.476±0.06 g/cm3(Predicted)
Storage Room temperature, dry, inert atmosphere

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 creating complex molecules for drug discovery. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build advanced intermediates in agrochemicals and medicinal chemistry. Also utilized in the preparation of functional materials where aromatic heterocycles are needed for electronic or optical properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿570.00
inventory 250mg
10-20 days ฿910.00
inventory 1g
10-20 days ฿3,310.00
inventory 5g
10-20 days ฿16,470.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-Bromo-5-phenoxypyridine
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 creating complex molecules for drug discovery. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build advanced intermediates in agrochemicals and medicinal chemistry. Also utilized in the preparation of functional materials where ar

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 creating complex molecules for drug discovery. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build advanced intermediates in agrochemicals and medicinal chemistry. Also utilized in the preparation of functional materials where aromatic heterocycles are needed for electronic or optical properties.

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...