3,4-bis((tert-butyldimethylsilyl)oxy)benzoic acid
95%
- Product Code: 151121
CAS:
154083-18-8
| Molecular Weight: | 382.64 g./mol | Molecular Formula: | C₁₉H₃₄O₄Si₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 395.0±32.0 °C(Predicted) | |
| Density: | 0.989±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature |
Product Description:
Used as a key intermediate in the synthesis of antiviral drugs, particularly in the preparation of HIV protease inhibitors. Its silyl-protected hydroxyl groups allow selective reactivity in multi-step organic syntheses, making it valuable in pharmaceutical development. The carboxylic acid functionality enables coupling reactions, facilitating the construction of complex molecular architectures. Commonly employed in research settings for modifying bioactive molecules where protection of phenolic groups is required.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White solid |
| Purity (%) | 94.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,410.00 |
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| 0.250 | 10-20 days | ฿2,340.00 |
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| 1.000 | 10-20 days | ฿4,680.00 |
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| 5.000 | 10-20 days | ฿22,230.00 |
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| 25.000 | 10-20 days | ฿105,590.00 |
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3,4-bis((tert-butyldimethylsilyl)oxy)benzoic acid
Used as a key intermediate in the synthesis of antiviral drugs, particularly in the preparation of HIV protease inhibitors. Its silyl-protected hydroxyl groups allow selective reactivity in multi-step organic syntheses, making it valuable in pharmaceutical development. The carboxylic acid functionality enables coupling reactions, facilitating the construction of complex molecular architectures. Commonly employed in research settings for modifying bioactive molecules where protection of phenolic groups is required.
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| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
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