Tert-Butyl (5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazol-2-yl)((2-(trimethylsilyl)ethoxy)methyl)carbamate
98%
- Product Code: 238173
CAS:
1228356-82-8
Molecular Weight: | 456.48 g./mol | Molecular Formula: | C₂₀H₃₇BN₂O₅SSi |
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EC Number: | MDL Number: | ||
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Density: | Storage Condition: | -20°C, Inert Gas |
Product Description:
Used primarily as an intermediate in the synthesis of pharmaceutical compounds, this chemical plays a key role in Suzuki-Miyaura cross-coupling reactions due to the presence of the boronate ester group. The thiazole ring serves as a common scaffold in bioactive molecules, making this compound valuable in drug discovery. The SEM (2-(trimethylsilyl)ethoxy)methyl protecting group ensures selective amine protection during multi-step syntheses, allowing controlled deprotection under mild conditions. Its main application is in the development of heterocyclic drugs, especially in oncology and antiviral research, where precise molecular construction is critical.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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100mg | 10-20 days | ฿5,840.00 |
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1g | 10-20 days | ฿24,210.00 |
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5g | 10-20 days | ฿84,700.00 |
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Tert-Butyl (5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazol-2-yl)((2-(trimethylsilyl)ethoxy)methyl)carbamate
Used primarily as an intermediate in the synthesis of pharmaceutical compounds, this chemical plays a key role in Suzuki-Miyaura cross-coupling reactions due to the presence of the boronate ester group. The thiazole ring serves as a common scaffold in bioactive molecules, making this compound valuable in drug discovery. The SEM (2-(trimethylsilyl)ethoxy)methyl protecting group ensures selective amine protection during multi-step syntheses, allowing controlled deprotection under mild conditions. Its main application is in the development of heterocyclic drugs, especially in oncology and antiviral research, where precise molecular construction is critical.
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