Tert-Butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-1-carboxylate
95%
- Product Code: 89488
CAS:
935278-73-2
Molecular Weight: | 293.17 g./mol | Molecular Formula: | C₁₅H₂₄BNO₄ |
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EC Number: | MDL Number: | MFCD11504966 | |
Melting Point: | Boiling Point: | 381.3±34.0 °C at 760 mmHg | |
Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
This chemical is primarily utilized as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronate ester group makes it a valuable reagent in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, the tert-butyl carboxylate group provides stability and protection for the pyrrole ring during chemical transformations, making it a useful building block in the preparation of heterocyclic compounds. Its applications extend to the production of biologically active molecules, including potential drug candidates and functional materials.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | Ft23,272.07 |
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0.250 | 10-20 days | Ft35,974.75 |
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1.000 | 10-20 days | Ft116,360.37 |
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Tert-Butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-1-carboxylate
This chemical is primarily utilized as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronate ester group makes it a valuable reagent in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, the tert-butyl carboxylate group provides stability and protection for the pyrrole ring during chemical transformations, making it a useful building block in the preparation of heterocyclic compounds. Its applications extend to the production of biologically active molecules, including potential drug candidates and functional materials.
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