1-Bromo-3-methyl-5-(trifluoromethoxy)benzene

95%

Reagent Code: #140735
fingerprint
CAS Number 887266-91-3

science Other reagents with same CAS 887266-91-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.03 g/mol
Formula C₈H₆BrF₃O
badge Registry Numbers
MDL Number MFCD07368791
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of active ingredients requiring fluorinated aromatic structures. Its bromo and trifluoromethoxy functional groups allow for selective cross-coupling reactions, making it valuable in building complex molecules for drug discovery and crop protection agents. Commonly employed in Suzuki, Heck, and other palladium-catalyzed reactions to introduce the 3-methyl-5-(trifluoromethoxy)phenyl moiety into target compounds. Also utilized in research settings for the preparation of novel organic materials and fluorinated analogs in medicinal chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿9,600.00
inventory 5g
10-20 days ฿28,800.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1-Bromo-3-methyl-5-(trifluoromethoxy)benzene
No image available

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of active ingredients requiring fluorinated aromatic structures. Its bromo and trifluoromethoxy functional groups allow for selective cross-coupling reactions, making it valuable in building complex molecules for drug discovery and crop protection agents. Commonly employed in Suzuki, Heck, and other palladium-catalyzed reactions to introduce the 3-methyl-5-(trifluoromethoxy)phenyl moiety into ta

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of active ingredients requiring fluorinated aromatic structures. Its bromo and trifluoromethoxy functional groups allow for selective cross-coupling reactions, making it valuable in building complex molecules for drug discovery and crop protection agents. Commonly employed in Suzuki, Heck, and other palladium-catalyzed reactions to introduce the 3-methyl-5-(trifluoromethoxy)phenyl moiety into target compounds. Also utilized in research settings for the preparation of novel organic materials and fluorinated analogs 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...