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

98%

  • Product Code: 209768
  CAS:    1025719-23-6
Molecular Weight: 276.06 g./mol Molecular Formula: C₁₁H₁₆BF₃N₂O₂
EC Number: MDL Number: MFCD12022323
Melting Point: 66-67°C Boiling Point:
Density: Storage Condition: -20°C, sealed, dry
Product Description: Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group facilitates coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in medicinal chemistry for constructing complex molecules. The presence of trifluoromethyl and methyl groups enhances electronic and metabolic stability in target compounds, often improving bioavailability and biological activity. It is especially useful in the development of fluorinated active pharmaceutical ingredients (APIs) where increased lipophilicity and resistance to oxidative degradation are required.
Sizes / Availability / Pricing:
Size Availability Price Quantity
250mg 10-20 days ฿960.00
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1g 10-20 days ฿2,400.00
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5g 10-20 days ฿9,590.00
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10g 10-20 days ฿18,800.00
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25g 10-20 days ฿47,000.00
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1-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-(trifluoromethyl)-1H-pyrazole
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group facilitates coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in medicinal chemistry for constructing complex molecules. The presence of trifluoromethyl and methyl groups enhances electronic and metabolic stability in target compounds, often improving bioavailability and biological activity. It is especially useful in the development of fluorinated active pharmaceutical ingredients (APIs) where increased lipophilicity and resistance to oxidative degradation are required.
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