(R,Z)-4-((tert-Butyldimethylsilyl)oxy)-N,N-diphenylpent-2-enamide
97%
- Product Code: 37793
CAS:
1820030-49-6
| Molecular Weight: | 381.58 g./mol | Molecular Formula: | C₂₃H₃₁NO₂Si |
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| EC Number: | MDL Number: | MFCD31381100 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring a tert-butyldimethylsilyl (TBS) protecting group, makes it valuable in multi-step synthetic processes, particularly in the protection of hydroxyl groups during chemical reactions. The presence of the diphenylamide moiety enhances its stability and reactivity, allowing it to participate in various coupling reactions. It is often employed in the synthesis of pharmaceuticals and bioactive compounds, where selective protection and deprotection strategies are crucial. Additionally, the compound’s stereochemistry (R,Z) can be leveraged in asymmetric synthesis to achieve specific chiral targets, making it a useful tool in the development of enantiomerically pure substances.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,519.00 |
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| 0.250 | 10-20 days | ฿5,868.00 |
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| 1.000 | 10-20 days | ฿17,613.00 |
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(R,Z)-4-((tert-Butyldimethylsilyl)oxy)-N,N-diphenylpent-2-enamide
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring a tert-butyldimethylsilyl (TBS) protecting group, makes it valuable in multi-step synthetic processes, particularly in the protection of hydroxyl groups during chemical reactions. The presence of the diphenylamide moiety enhances its stability and reactivity, allowing it to participate in various coupling reactions. It is often employed in the synthesis of pharmaceuticals and bioactive compounds, where selective protection and deprotection strategies are crucial. Additionally, the compound’s stereochemistry (R,Z) can be leveraged in asymmetric synthesis to achieve specific chiral targets, making it a useful tool in the development of enantiomerically pure substances.
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