(R)-Methyl 3-((tert-butyldimethylsilyl)oxy)hex-5-enoate
95%
- Product Code: 82969
CAS:
121980-44-7
| Molecular Weight: | 258.43 g./mol | Molecular Formula: | C₁₃H₂₆O₃Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30566060 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in organic synthesis, particularly in the construction of complex molecules. It serves as a key intermediate in the production of pharmaceuticals and bioactive compounds. The tert-butyldimethylsilyl (TBDMS) group acts as a protecting group for the hydroxyl functionality, allowing selective reactions to occur at other sites of the molecule. The compound is also valuable in asymmetric synthesis, where the (R)-configuration plays a critical role in achieving enantioselective transformations. Its application extends to the development of chiral building blocks for drug discovery and natural product synthesis. Additionally, the presence of the hex-5-enoate moiety makes it useful in reactions involving olefin metathesis or cross-coupling, enabling the formation of carbon-carbon bonds in target molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,890.00 |
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| 0.250 | 10-20 days | ฿3,375.00 |
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| 1.000 | 10-20 days | ฿6,750.00 |
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(R)-Methyl 3-((tert-butyldimethylsilyl)oxy)hex-5-enoate
This chemical is primarily used in organic synthesis, particularly in the construction of complex molecules. It serves as a key intermediate in the production of pharmaceuticals and bioactive compounds. The tert-butyldimethylsilyl (TBDMS) group acts as a protecting group for the hydroxyl functionality, allowing selective reactions to occur at other sites of the molecule. The compound is also valuable in asymmetric synthesis, where the (R)-configuration plays a critical role in achieving enantioselective transformations. Its application extends to the development of chiral building blocks for drug discovery and natural product synthesis. Additionally, the presence of the hex-5-enoate moiety makes it useful in reactions involving olefin metathesis or cross-coupling, enabling the formation of carbon-carbon bonds in target molecules.
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