1-Bromo-5-chloro-2,3-difluorobenzene

98%

Reagent Code: #40048
fingerprint
CAS Number 1160573-26-1

science Other reagents with same CAS 1160573-26-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.43 g/mol
Formula C₆H₂BrClF₂
badge Registry Numbers
MDL Number MFCD11845996
inventory_2 Storage & Handling
Storage room temperature

description Product Description

1-Bromo-5-chloro-2,3-difluorobenzene is primarily utilized as a versatile intermediate in organic synthesis. Its unique combination of halogen substituents makes it valuable for constructing complex molecules, particularly in pharmaceutical and agrochemical research. The compound is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce aromatic structures with specific halogen patterns. These reactions are crucial for developing active pharmaceutical ingredients (APIs) or advanced materials. Additionally, its halogen-rich structure allows for further functionalization, enabling the creation of diverse chemical entities for drug discovery or specialty chemical applications. The presence of fluorine atoms also enhances the metabolic stability and bioavailability of resulting compounds, making it a preferred choice in medicinal chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿20,592.00
inventory 1g
10-20 days ฿4,482.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1-Bromo-5-chloro-2,3-difluorobenzene
No image available
1-Bromo-5-chloro-2,3-difluorobenzene is primarily utilized as a versatile intermediate in organic synthesis. Its unique combination of halogen substituents makes it valuable for constructing complex molecules, particularly in pharmaceutical and agrochemical research. The compound is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce aromatic structures with specific halogen patterns. These reactions are crucial for developing active pharmaceutical ingredients (APIs) or advanced materials. Additionally, its halogen-rich structure allows for further functionalization, enabling the creation of diverse chemical entities for drug discovery or specialty chemical applications. The presence of fluorine atoms also enhances the metabolic stability and bioavailability of resulting compounds, making it a preferred choice in medicinal chemistry.
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...