((1R,3S,E)-5-((E)-2-((1R,3As,7Ar)-7A-Methyl-1-((R)-6-Methylheptan-2-Yl)Dihydro-1H-Inden-4(2H,5H,6H,7H,7Ah)-Ylidene)Ethylidene)-4-Methylenecyclohexane-1,3-Diyl)Bis(Oxy)Bis(Tert-Butyldimethylsilane)
98%
- Product Code: 231778
CAS:
112670-85-6
| Molecular Weight: | 629.16 g./mol | Molecular Formula: | C₃₉H₇₂O₂Si₂ |
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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 the synthesis of complex natural products and bioactive molecules, particularly in pharmaceutical research involving steroidal and terpenoid frameworks. Its functionalized cyclohexane core and silyl-protected hydroxyl groups enable selective transformations in multi-step organic syntheses. The compound's stereochemistry and olefin moieties allow for controlled reactions such as cross-metathesis, hydrogenation, and directed C–H functionalization. It is especially valuable in constructing polycyclic systems found in anti-inflammatory, anticancer, and neuroactive agents. The tert-butyldimethylsilyl (TBS) protecting groups ensure stability during sequential reactions, making it suitable for use in automated and high-throughput synthesis platforms.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿5,030.00 |
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| 250mg | 10-20 days | ฿8,370.00 |
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| 1g | 10-20 days | ฿20,530.00 |
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((1R,3S,E)-5-((E)-2-((1R,3As,7Ar)-7A-Methyl-1-((R)-6-Methylheptan-2-Yl)Dihydro-1H-Inden-4(2H,5H,6H,7H,7Ah)-Ylidene)Ethylidene)-4-Methylenecyclohexane-1,3-Diyl)Bis(Oxy)Bis(Tert-Butyldimethylsilane)
Used as a key intermediate in the synthesis of complex natural products and bioactive molecules, particularly in pharmaceutical research involving steroidal and terpenoid frameworks. Its functionalized cyclohexane core and silyl-protected hydroxyl groups enable selective transformations in multi-step organic syntheses. The compound's stereochemistry and olefin moieties allow for controlled reactions such as cross-metathesis, hydrogenation, and directed C–H functionalization. It is especially valuable in constructing polycyclic systems found in anti-inflammatory, anticancer, and neuroactive agents. The tert-butyldimethylsilyl (TBS) protecting groups ensure stability during sequential reactions, making it suitable for use in automated and high-throughput synthesis platforms.
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