5-Methyl-1-(tetrahydro-2H-pyran-2-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
98%
- Product Code: 203010
CAS:
1072709-32-0
Molecular Weight: | 292.18 g./mol | Molecular Formula: | C₁₅H₂₅BN₂O₃ |
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EC Number: | MDL Number: | MFCD22572261 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. The presence of the boronate ester group allows for efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules. Its protected pyrazole ring offers stability during reaction sequences and can be deprotected to reveal active nitrogen functionalities later in the synthesis. This compound is particularly useful in medicinal chemistry for constructing substituted pyrazole derivatives, which are common motifs in bioactive compounds and drug candidates.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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100mg | 10-20 days | $290.75 |
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1g | 10-20 days | $1,285.46 |
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5-Methyl-1-(tetrahydro-2H-pyran-2-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. The presence of the boronate ester group allows for efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules. Its protected pyrazole ring offers stability during reaction sequences and can be deprotected to reveal active nitrogen functionalities later in the synthesis. This compound is particularly useful in medicinal chemistry for constructing substituted pyrazole derivatives, which are common motifs in bioactive compounds and drug candidates.
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