9-bromo-2,3-diiodo-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine

≥95%

Reagent Code: #142088
fingerprint
CAS Number 1282516-68-0

science Other reagents with same CAS 1282516-68-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 516.90 g/mol
Formula C₁₁H₇BrI₂N₂O
badge Registry Numbers
MDL Number MFCD28358731
inventory_2 Storage & Handling
Storage 2-8 °C, Sealed, Dry, Lightproof, Inert Gas

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and functional materials, particularly in cross-coupling reactions due to the presence of multiple halogen atoms. The bromo and iodo groups allow selective functionalization through metal-catalyzed reactions such as Suzuki, Stille, or Ullmann couplings. Its rigid polycyclic structure makes it suitable for developing bioactive compounds, especially in medicinal chemistry for designing kinase inhibitors or receptor modulators. Also explored in materials science for constructing conjugated systems in optoelectronic devices.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,380.00
inventory 250mg
10-20 days ฿4,050.00
inventory 1g
10-20 days ฿7,290.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
9-bromo-2,3-diiodo-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine
No image available

Used in organic synthesis as an intermediate for pharmaceuticals and functional materials, particularly in cross-coupling reactions due to the presence of multiple halogen atoms. The bromo and iodo groups allow selective functionalization through metal-catalyzed reactions such as Suzuki, Stille, or Ullmann couplings. Its rigid polycyclic structure makes it suitable for developing bioactive compounds, especially in medicinal chemistry for designing kinase inhibitors or receptor modulators. Also explored i

Used in organic synthesis as an intermediate for pharmaceuticals and functional materials, particularly in cross-coupling reactions due to the presence of multiple halogen atoms. The bromo and iodo groups allow selective functionalization through metal-catalyzed reactions such as Suzuki, Stille, or Ullmann couplings. Its rigid polycyclic structure makes it suitable for developing bioactive compounds, especially in medicinal chemistry for designing kinase inhibitors or receptor modulators. Also explored in materials science for constructing conjugated systems in optoelectronic devices.

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...