1-(tert-Butyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
97%
Reagent
Code: #148514
CAS Number
1256359-15-5
blur_circular Chemical Specifications
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Molecular Information
Weight
250.15 g/mol
Formula
C₁₃H₂₃BN₂O₂
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Registry Numbers
MDL Number
MFCD16660302
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Storage & Handling
Storage
-20°C, stored in inert gas
description Product Description
Used in cross-coupling reactions, particularly in Suzuki-Miyaura coupling, to introduce the pyrazole moiety into organic molecules. This enables the synthesis of biologically active compounds, including pharmaceuticals and agrochemicals, where pyrazole derivatives are common structural motifs. The boronate ester group acts as a handle for palladium-catalyzed bond formation, making it valuable in medicinal chemistry and drug discovery for building complex heterocyclic systems. It is also employed in materials science for constructing functional organic molecules with tailored electronic properties.
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