4-chloro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidine
≥95%
- Product Code: 191855
CAS:
1830311-70-0
| Molecular Weight: | 409.7907 g./mol | Molecular Formula: | C₁₈H₂₉BClN₃O₃Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30803195 | |
| Melting Point: | Boiling Point: | 495.0±45.0 °C(Predicted) | |
| Density: | 1.15±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C |
Product Description:
Used in pharmaceutical synthesis as a key intermediate in the preparation of kinase inhibitors, particularly for targeted cancer therapies. Its boronate ester functionality enables Suzuki-Miyaura cross-coupling reactions, allowing efficient construction of complex heterocyclic systems found in bioactive molecules. The SEM (trimethylsilylethoxymethyl) protecting group ensures selective reactivity during multi-step synthesis, making it valuable in the development of potent drug candidates targeting oncogenic signaling pathways.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 G | 10-20 days | ฿1,730.00 |
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| 0.250 G | 10-20 days | ฿2,800.00 |
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| 1.000 G | 10-20 days | ฿7,430.00 |
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| 5.000 G | 10-20 days | ฿30,900.00 |
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4-chloro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidine
Used in pharmaceutical synthesis as a key intermediate in the preparation of kinase inhibitors, particularly for targeted cancer therapies. Its boronate ester functionality enables Suzuki-Miyaura cross-coupling reactions, allowing efficient construction of complex heterocyclic systems found in bioactive molecules. The SEM (trimethylsilylethoxymethyl) protecting group ensures selective reactivity during multi-step synthesis, making it valuable in the development of potent drug candidates targeting oncogenic signaling pathways.
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