1-Isobutyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole

96%

Reagent Code: #200400
fingerprint
CAS Number 827614-66-4

science Other reagents with same CAS 827614-66-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.14 g/mol
Formula C₁₃H₂₃BN₂O₂
badge Registry Numbers
MDL Number MFCD05663857
thermostat Physical Properties
Boiling Point 248 - 249 ℃ - lit.
inventory_2 Storage & Handling
Density 1.003 g/mL at 25℃(lit.)
Storage 2-8°C

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The presence of the pyrazole ring allows for further functionalization, enhancing its utility in building bioactive compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿660.00
inventory 1g
10-20 days ฿1,460.00
inventory 5g
10-20 days ฿4,340.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1-Isobutyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
No image available

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The presence of the pyrazole ring allows for further functionalization, enhancing its utility in building bio

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The presence of the pyrazole ring allows for further functionalization, enhancing its utility in building bioactive compounds.

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...