3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)pyridine

98%

Reagent Code: #240753
fingerprint
CAS Number 1084953-47-8

science Other reagents with same CAS 1084953-47-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 273.06 g/mol
Formula C₁₂H₁₅BF₃NO₂
thermostat Physical Properties
Boiling Point 357.9°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in medicinal chemistry for constructing biaryl systems. The presence of a trifluoromethyl-substituted pyridine enhances metabolic stability and lipophilicity in drug candidates. It is particularly useful in the development of bioactive molecules where fluorinated heteroaromatic motifs are required. Its stability and reactivity profile make it suitable for automated synthesis and high-throughput screening in drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿700.00
inventory 1g
10-20 days ฿1,620.00
inventory 5g
10-20 days ฿7,880.00
inventory 10g
10-20 days ฿15,700.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)pyridine
No image available

Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in medicinal chemistry for constructing biaryl systems. The presence of a trifluoromethyl-substituted pyridine enhances metabolic stability and lipophilicity in drug candidates. It is particularly useful in the development of bioactive mol

Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in medicinal chemistry for constructing biaryl systems. The presence of a trifluoromethyl-substituted pyridine enhances metabolic stability and lipophilicity in drug candidates. It is particularly useful in the development of bioactive molecules where fluorinated heteroaromatic motifs are required. Its stability and reactivity profile make it suitable for automated synthesis and high-throughput screening in drug discovery.

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...