3-(Benzyloxy)-6-(((tert-butyldimethylsilyl)oxy)methyl)-4-oxo-4H-pyran-2-carboxylic acid
97%
- Product Code: 44608
CAS:
895134-29-9
| Molecular Weight: | 390.50 g./mol | Molecular Formula: | C₂₀H₂₆O₆Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26959170 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules, particularly in the pharmaceutical and agrochemical industries. Its structure, featuring both benzyloxy and tert-butyldimethylsilyl (TBDMS) protecting groups, makes it valuable in multi-step synthetic processes where selective deprotection is required. The compound is often employed in the synthesis of pyran-based derivatives, which are key building blocks for developing biologically active compounds, including potential drug candidates. Additionally, its carboxylic acid functionality allows for further chemical modifications, enabling the creation of esters, amides, or other derivatives for targeted applications in medicinal chemistry.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 G | 10-20 days | ฿4,887.00 |
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| 0.250 G | 10-20 days | ฿7,830.00 |
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| 1.000 G | 10-20 days | ฿19,593.00 |
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3-(Benzyloxy)-6-(((tert-butyldimethylsilyl)oxy)methyl)-4-oxo-4H-pyran-2-carboxylic acid
This chemical is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules, particularly in the pharmaceutical and agrochemical industries. Its structure, featuring both benzyloxy and tert-butyldimethylsilyl (TBDMS) protecting groups, makes it valuable in multi-step synthetic processes where selective deprotection is required. The compound is often employed in the synthesis of pyran-based derivatives, which are key building blocks for developing biologically active compounds, including potential drug candidates. Additionally, its carboxylic acid functionality allows for further chemical modifications, enabling the creation of esters, amides, or other derivatives for targeted applications in medicinal chemistry.
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