tert-Butyl 2-oxo-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)spiro[indoline-3,4'-piperidine]-1'-carboxylate
95%
- Product Code: 42501
CAS:
1253288-12-8
| Molecular Weight: | 428.3295 g./mol | Molecular Formula: | C₂₃H₃₃BN₂O₅ |
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| EC Number: | MDL Number: | MFCD16618542 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and biologically active molecules. It serves as a key intermediate in the construction of complex organic structures due to the presence of both the spiro[indoline-3,4'-piperidine] scaffold and the boronate ester group. The boronate ester functionality enables its use in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds in drug discovery and material science. Additionally, the tert-butyl carbamate (Boc) protecting group enhances its stability during synthetic processes, making it a valuable building block for the synthesis of nitrogen-containing heterocycles. Its applications extend to the preparation of potential therapeutic agents, particularly in the fields of oncology and central nervous system disorders, where such structural motifs are often explored.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿11,295.00 |
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tert-Butyl 2-oxo-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)spiro[indoline-3,4'-piperidine]-1'-carboxylate
This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and biologically active molecules. It serves as a key intermediate in the construction of complex organic structures due to the presence of both the spiro[indoline-3,4'-piperidine] scaffold and the boronate ester group. The boronate ester functionality enables its use in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds in drug discovery and material science. Additionally, the tert-butyl carbamate (Boc) protecting group enhances its stability during synthetic processes, making it a valuable building block for the synthesis of nitrogen-containing heterocycles. Its applications extend to the preparation of potential therapeutic agents, particularly in the fields of oncology and central nervous system disorders, where such structural motifs are often explored.
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