1-(2-Methoxyethyl)-3,5-dimethyl-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
95%
- Product Code: 39247
CAS:
1200537-40-1
Molecular Weight: | 280.1709 g./mol | Molecular Formula: | C₁₄H₂₅BN₂O₃ |
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EC Number: | MDL Number: | MFCD22572270 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile building block, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a pyrazole ring and a boronate ester group, makes it valuable for Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in complex molecule construction. Additionally, it serves as an intermediate in the preparation of biologically active compounds, including potential drug candidates targeting various diseases. The methoxyethyl group enhances its solubility and reactivity in organic solvents, facilitating its use in diverse chemical processes. Its stability and functional groups also make it suitable for applications in material science, such as the synthesis of advanced polymers and coatings.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | Ft28,120.42 |
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1-(2-Methoxyethyl)-3,5-dimethyl-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
This chemical is primarily utilized in organic synthesis as a versatile building block, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a pyrazole ring and a boronate ester group, makes it valuable for Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in complex molecule construction. Additionally, it serves as an intermediate in the preparation of biologically active compounds, including potential drug candidates targeting various diseases. The methoxyethyl group enhances its solubility and reactivity in organic solvents, facilitating its use in diverse chemical processes. Its stability and functional groups also make it suitable for applications in material science, such as the synthesis of advanced polymers and coatings.
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