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

98%

Reagent Code: #152089
fingerprint
CAS Number 1488423-70-6

science Other reagents with same CAS 1488423-70-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.15 g/mol
Formula C₁₃H₂₃BN₂O₂
badge Registry Numbers
MDL Number MFCD17014638
inventory_2 Storage & Handling
Storage 2-8°C, dry

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 and selective coupling with aryl or heteroaryl halides under palladium catalysis. Commonly employed in the preparation of biologically active compounds, including drug candidates containing pyrazole scaffolds. Suitable for use in late-stage functionalization due to its stability and reactivity profile. Also applied in materials science for constructing conjugated systems in organic electronics.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,360.00
inventory 5g
10-20 days ฿13,440.00
inventory 25g
10-20 days ฿50,950.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1-Butyl-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 and selective coupling with aryl or heteroaryl halides under palladium catalysis. Commonly employed in the preparation of biologically active compounds, including drug candidates containing pyrazole scaffolds. Suitable for use in late-stage functionalization due to its stability and reactivity prof

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 and selective coupling with aryl or heteroaryl halides under palladium catalysis. Commonly employed in the preparation of biologically active compounds, including drug candidates containing pyrazole scaffolds. Suitable for use in late-stage functionalization due to its stability and reactivity profile. Also applied in materials science for constructing conjugated systems in organic electronics.

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...