1-Methylpyrazole-4-boronic acid pinacol ester

97%

  • Product Code: 89509
  Alias:    N-methylpyrazole-4-boronic acid pinacol ester 1-Methyl-1H-pyrazole-4-boronic acid pinacid; 1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolane- 2-yl)-1H-pyrazole
  CAS:    761446-44-0
Molecular Weight: 208.07 g./mol Molecular Formula: C₁₀H₁₇BN₂O₂
EC Number: MDL Number: MFCD03789259
Melting Point: 59-64 °C(lit.) Boiling Point:
Density: Storage Condition: 2~8°C, combustible area
Product Description: This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex molecules, especially in pharmaceutical and agrochemical research. The boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug development. Additionally, it is employed in material science for designing organic electronic materials and polymers. Its stability and reactivity make it a valuable reagent in various catalytic processes, contributing to advancements in medicinal chemistry and functional materials.
Product Specification:
Test Specification
Melting point 59 64?
PurityGC 97 100%
APPEARANCE POWDER CRYSTALS AND/OR CHUNKS
INFRARED SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days ฿290.00
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1.000 10-20 days ฿310.00
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5.000 10-20 days ฿360.00
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25.000 10-20 days ฿1,110.00
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100.000 10-20 days ฿4,250.00
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1-Methylpyrazole-4-boronic acid pinacol ester
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex molecules, especially in pharmaceutical and agrochemical research. The boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug development. Additionally, it is employed in material science for designing organic electronic materials and polymers. Its stability and reactivity make it a valuable reagent in various catalytic processes, contributing to advancements in medicinal chemistry and functional materials.
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