(2-(3-(trifluoromethyl)phenyl)pyrimidin-5-yl)boronic acid

95%

Reagent Code: #56308
fingerprint
CAS Number 2225175-12-0

science Other reagents with same CAS 2225175-12-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 267.9996296 g/mol
Formula C₁₁H₈BF₃N₂O₂
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group allows it to form stable covalent bonds with various organic molecules, making it valuable in constructing complex chemical structures. Additionally, it is employed in the development of bioactive compounds and in research for drug discovery, where it aids in creating molecules with potential therapeutic properties. Its trifluoromethyl group enhances its stability and reactivity, making it suitable for applications in diverse chemical processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿10,660.00
inventory 25mg
10-20 days ฿32,000.00
inventory 100mg
10-20 days ฿110,000.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(2-(3-(trifluoromethyl)phenyl)pyrimidin-5-yl)boronic acid
No image available

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group allows it to form stable covalent bonds with various organic molecules, making it valuable in constructing complex chemical structures. Additionally, it is employed in the development of bioactive compounds and in research for drug discovery

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group allows it to form stable covalent bonds with various organic molecules, making it valuable in constructing complex chemical structures. Additionally, it is employed in the development of bioactive compounds and in research for drug discovery, where it aids in creating molecules with potential therapeutic properties. Its trifluoromethyl group enhances its stability and reactivity, making it suitable for applications in diverse chemical 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...