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

95%

Reagent Code: #149889
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CAS Number 2096332-26-0

science Other reagents with same CAS 2096332-26-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.14 g/mol
Formula C₁₃H₂₃BN₂O₂
badge Registry Numbers
MDL Number MFCD21333036
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-carbon bonds under mild conditions. It is especially valuable in constructing complex pyrazole-based structures found in bioactive molecules. The butyl group enhances solubility and stability, improving reaction yields in late-stage functionalization of drug candidates. Commonly employed in medicinal chemistry for lead optimization and library synthesis.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿17,860.00
inventory 5g
10-20 days ฿47,410.00

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1-Butyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
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Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-carbon bonds under mild conditions. It is especially valuable in constructing complex pyrazole-based structures found in bioactive molecules. The butyl group enhances solubility and stability, improving reaction yields in late-stage functionalization of drug candida

Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-carbon bonds under mild conditions. It is especially valuable in constructing complex pyrazole-based structures found in bioactive molecules. The butyl group enhances solubility and stability, improving reaction yields in late-stage functionalization of drug candidates. Commonly employed in medicinal chemistry for lead optimization and library synthesis.

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