(R)-6-((1R,3As,7Ar,E)-4-((Z)-2-((3S,5R)-3,5-Bis(Tert-Butyldimethylsilyloxy)-2-Methylenecyclohexylidene)Ethylidene)-7A-Methyloctahydro-1H-Inden-1-Yl)-2-Methylheptan-2-Ol
98%
- Product Code: 231606
CAS:
140710-96-9
| Molecular Weight: | 645.16 g./mol | Molecular Formula: | C₃₉H₇₂O₃Si₂ |
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| Density: | Storage Condition: | Room temperature |
Product Description:
Used in advanced organic synthesis, particularly in the preparation of complex natural products and pharmaceutical intermediates. Its highly functionalized structure, with multiple stereocenters and protected hydroxyl groups, makes it a valuable chiral building block for constructing bioactive molecules, especially in the development of vitamin D analogs and other steroid-like compounds. The tert-butyldimethylsilyl (TBS) protecting groups allow selective deprotection and further derivatization, enabling stepwise synthesis in multi-step reaction sequences. Commonly employed in research settings for total synthesis of terpenoids and related polycyclic compounds.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | Ft395,049.88 |
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(R)-6-((1R,3As,7Ar,E)-4-((Z)-2-((3S,5R)-3,5-Bis(Tert-Butyldimethylsilyloxy)-2-Methylenecyclohexylidene)Ethylidene)-7A-Methyloctahydro-1H-Inden-1-Yl)-2-Methylheptan-2-Ol
Used in advanced organic synthesis, particularly in the preparation of complex natural products and pharmaceutical intermediates. Its highly functionalized structure, with multiple stereocenters and protected hydroxyl groups, makes it a valuable chiral building block for constructing bioactive molecules, especially in the development of vitamin D analogs and other steroid-like compounds. The tert-butyldimethylsilyl (TBS) protecting groups allow selective deprotection and further derivatization, enabling stepwise synthesis in multi-step reaction sequences. Commonly employed in research settings for total synthesis of terpenoids and related polycyclic compounds.
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