((1R,3S,E)-5-((E)-2-((1R,3As,7Ar)-1-((2R,5R,E)-5,6-Dimethylhept-3-En-2-Yl)-7A-Methyldihydro-1H-Inden-4(2H,5H,6H,7H,7Ah)-Ylidene)Ethylidene)-4-Methylenecyclohexane-1,3-Diyl)Bis(Oxy)Bis(Tert-Butyldimeth Ylsilane)
97%
- Product Code: 231779
CAS:
111594-58-2
| Molecular Weight: | 641.17 g./mol | Molecular Formula: | C₄₀H₇₂O₂Si₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature |
Product Description:
Used as a specialized protecting group reagent in complex organic synthesis, particularly in the construction of polyene natural products and stereochemically sensitive molecules. Its structure allows for selective protection of diol functionalities, enabling stepwise manipulation of reactive sites in multi-step syntheses. Commonly applied in the preparation of bioactive terpenoids and macrolide derivatives where precise stereocontrol and functional group compatibility are critical. The tert-butyldimethylsilyl (TBDMS) groups provide steric bulk and stability under various reaction conditions, while the core scaffold supports conformational rigidity, aiding in stereoselective transformations.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿5,150.00 |
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((1R,3S,E)-5-((E)-2-((1R,3As,7Ar)-1-((2R,5R,E)-5,6-Dimethylhept-3-En-2-Yl)-7A-Methyldihydro-1H-Inden-4(2H,5H,6H,7H,7Ah)-Ylidene)Ethylidene)-4-Methylenecyclohexane-1,3-Diyl)Bis(Oxy)Bis(Tert-Butyldimeth Ylsilane)
Used as a specialized protecting group reagent in complex organic synthesis, particularly in the construction of polyene natural products and stereochemically sensitive molecules. Its structure allows for selective protection of diol functionalities, enabling stepwise manipulation of reactive sites in multi-step syntheses. Commonly applied in the preparation of bioactive terpenoids and macrolide derivatives where precise stereocontrol and functional group compatibility are critical. The tert-butyldimethylsilyl (TBDMS) groups provide steric bulk and stability under various reaction conditions, while the core scaffold supports conformational rigidity, aiding in stereoselective transformations.
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