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

95%

Reagent Code: #58133
fingerprint
CAS Number 2225171-63-9

science Other reagents with same CAS 2225171-63-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.9914096 g/mol
Formula C₁₀H₁₀BF₃O₂
inventory_2 Storage & Handling
Storage -20℃

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable for creating aryl-aryl or aryl-heteroaryl linkages. This is essential for developing active pharmaceutical ingredients (APIs) or advanced materials. Additionally, its trifluoromethyl group enhances the stability and bioavailability of the resulting compounds, making it a preferred choice in drug discovery and development processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿16,092.00
inventory 25mg
10-20 days ฿32,292.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(2-cyclopropyl-5-(trifluoromethyl)phenyl)boronic acid
No image available

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable for creating aryl-aryl or aryl-heteroaryl linkages. This is essential for developing active pharmaceutical ingredients (APIs) or advanced materials. Additi

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable for creating aryl-aryl or aryl-heteroaryl linkages. This is essential for developing active pharmaceutical ingredients (APIs) or advanced materials. Additionally, its trifluoromethyl group enhances the stability and bioavailability of the resulting compounds, making it a preferred choice in drug discovery and development processes.

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...