3-((tert-butyldimethylsilyl)oxy)propyl 4-methylbenzenesulfonate
95%
- Product Code: 242906
CAS:
115306-83-7
| Molecular Weight: | 344.54 g./mol | Molecular Formula: | C₁₆H₂₈O₄SSi |
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| EC Number: | MDL Number: | ||
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| Density: | Storage Condition: | Room temperature |
Product Description:
Used as a key intermediate in organic synthesis, particularly in the protection and activation of hydroxyl groups during complex molecule assembly. Its primary application lies in the pharmaceutical and agrochemical industries, where it enables selective functionalization in multi-step syntheses. The silyl ether group acts as a protecting group for alcohols, while the tosylate moiety serves as a good leaving group, facilitating nucleophilic substitution reactions. This dual functionality makes it valuable for constructing carbon-oxygen and carbon-carbon bonds in sensitive or sterically hindered systems. It is also employed in the synthesis of natural products and bioactive molecules where precise control over reactivity and regioselectivity is required.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $96.00 |
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| 0.250 | 10-20 days | $160.35 |
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| 1.000 | 10-20 days | $320.69 |
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3-((tert-butyldimethylsilyl)oxy)propyl 4-methylbenzenesulfonate
Used as a key intermediate in organic synthesis, particularly in the protection and activation of hydroxyl groups during complex molecule assembly. Its primary application lies in the pharmaceutical and agrochemical industries, where it enables selective functionalization in multi-step syntheses. The silyl ether group acts as a protecting group for alcohols, while the tosylate moiety serves as a good leaving group, facilitating nucleophilic substitution reactions. This dual functionality makes it valuable for constructing carbon-oxygen and carbon-carbon bonds in sensitive or sterically hindered systems. It is also employed in the synthesis of natural products and bioactive molecules where precise control over reactivity and regioselectivity is required.
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