(2-Isopropoxy-5-(trifluoromethyl)phenyl)boronic acid

98%

Reagent Code: #201040
fingerprint
CAS Number 850593-12-3

science Other reagents with same CAS 850593-12-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.01 g/mol
Formula C₁₀H₁₂BF₃O₃
badge Registry Numbers
MDL Number MFCD07363786
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, inert gas

description Product Description

Used in Suzuki-Miyaura cross-coupling reactions to synthesize complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic acid group enables formation of carbon-carbon bonds with aryl halides, facilitating the construction of biaryl structures. The trifluoromethyl and isopropoxy substituents enhance electronic and steric properties, improving selectivity and stability in reaction pathways. Commonly employed in the development of bioactive compounds and functional materials.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,360.00
inventory 1g
10-20 days ฿3,500.00
inventory 5g
10-20 days ฿10,870.00
(2-Isopropoxy-5-(trifluoromethyl)phenyl)boronic acid
No image available

Used in Suzuki-Miyaura cross-coupling reactions to synthesize complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic acid group enables formation of carbon-carbon bonds with aryl halides, facilitating the construction of biaryl structures. The trifluoromethyl and isopropoxy substituents enhance electronic and steric properties, improving selectivity and stability in reaction pathways. Commonly employed in the development of bioactive compounds and functional mate

Used in Suzuki-Miyaura cross-coupling reactions to synthesize complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic acid group enables formation of carbon-carbon bonds with aryl halides, facilitating the construction of biaryl structures. The trifluoromethyl and isopropoxy substituents enhance electronic and steric properties, improving selectivity and stability in reaction pathways. Commonly employed in the development of bioactive compounds and functional materials.

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...