2-Bromo-1-methoxy-4-(trifluoromethyl)benzene

95%

Reagent Code: #145931
fingerprint
CAS Number 402-10-8

science Other reagents with same CAS 402-10-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.03 g/mol
Formula C₈H₆BrF₃O
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in reactions where a bromine-functionalized aromatic ring is needed for coupling processes. Its methoxy and trifluoromethyl groups provide electronic and steric properties that enhance reactivity in metal-catalyzed reactions like Suzuki or Heck couplings. Commonly employed in the development of bioactive molecules, including antifungal agents and herbicides, due to the stability and lipophilicity imparted by the trifluoromethyl group. Also utilized in materials science for constructing functionalized aromatic systems in organic semiconductors.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,680.00
inventory 25g
10-20 days ฿5,600.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-Bromo-1-methoxy-4-(trifluoromethyl)benzene
No image available

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in reactions where a bromine-functionalized aromatic ring is needed for coupling processes. Its methoxy and trifluoromethyl groups provide electronic and steric properties that enhance reactivity in metal-catalyzed reactions like Suzuki or Heck couplings. Commonly employed in the development of bioactive molecules, including antifungal agents and herbicides, due to the stability and lipophilicity imparted by the t

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in reactions where a bromine-functionalized aromatic ring is needed for coupling processes. Its methoxy and trifluoromethyl groups provide electronic and steric properties that enhance reactivity in metal-catalyzed reactions like Suzuki or Heck couplings. Commonly employed in the development of bioactive molecules, including antifungal agents and herbicides, due to the stability and lipophilicity imparted by the trifluoromethyl group. Also utilized in materials science for constructing functionalized aromatic systems in organic semiconductors.

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...