((1R,3S,E)-5-((E)-2-((1R,3aS,7aR)-1-((2R,5S)-5,6-dimethylheptan-2-yl)-7a-methyldihydro-1H-inden-4(2H,5H,6H,7H,7aH)-ylidene)ethylidene)-4-methylenecyclohexane-1,3-diyl)bis(oxy)bis(tert-butyldimethylsilane)

98%

Reagent Code: #231899
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CAS Number 2229745-37-1

science Other reagents with same CAS 2229745-37-1

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Weight 643.19 g/mol
Formula C₄₀H₇₄O₂Si₂
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of complex natural products and bioactive molecules, particularly in the pharmaceutical industry for developing steroidal and terpenoid derivatives. Its functionalized cyclohexane core and silyl-protected hydroxyl groups allow selective deprotection and coupling reactions, enabling precise construction of intricate molecular architectures. Commonly employed in multi-step organic syntheses where stereochemical control and orthogonal protection are critical.

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inventory 5mg
10-20 days ฿54,450.00

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((1R,3S,E)-5-((E)-2-((1R,3aS,7aR)-1-((2R,5S)-5,6-dimethylheptan-2-yl)-7a-methyldihydro-1H-inden-4(2H,5H,6H,7H,7aH)-ylidene)ethylidene)-4-methylenecyclohexane-1,3-diyl)bis(oxy)bis(tert-butyldimethylsilane)
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Used as a key intermediate in the synthesis of complex natural products and bioactive molecules, particularly in the pharmaceutical industry for developing steroidal and terpenoid derivatives. Its functionalized cyclohexane core and silyl-protected hydroxyl groups allow selective deprotection and coupling reactions, enabling precise construction of intricate molecular architectures. Commonly employed in multi-step organic syntheses where stereochemical control and orthogonal protection are critical.

Used as a key intermediate in the synthesis of complex natural products and bioactive molecules, particularly in the pharmaceutical industry for developing steroidal and terpenoid derivatives. Its functionalized cyclohexane core and silyl-protected hydroxyl groups allow selective deprotection and coupling reactions, enabling precise construction of intricate molecular architectures. Commonly employed in multi-step organic syntheses where stereochemical control and orthogonal protection are critical.

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