(1S,3Ar,7Ar)-7A-Methyl-1-((S)-1-(3-Methyl-3-((Trimethylsilyl)Oxy)Butoxy)Ethyl)Octahydro-4H-Inden-4-One

97%

Reagent Code: #237358
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CAS Number 192573-33-4

science Other reagents with same CAS 192573-33-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 354.6 g/mol
Formula C₂₀H₃₈O₃Si
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in advanced organic synthesis as a chiral intermediate for pharmaceuticals, particularly in the development of steroid-like compounds and hormone analogs. Its complex stereochemistry makes it valuable for constructing biologically active molecules with high enantioselectivity. Commonly employed in research settings to design enzyme inhibitors and receptor modulators. The trimethylsilyl group acts as a protecting group, facilitating selective reactions in multi-step synthesis. Not typically used in industrial applications outside of specialized medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿17,350.00
inventory 250mg
10-20 days ฿28,910.00
inventory 1g
10-20 days ฿70,970.00
(1S,3Ar,7Ar)-7A-Methyl-1-((S)-1-(3-Methyl-3-((Trimethylsilyl)Oxy)Butoxy)Ethyl)Octahydro-4H-Inden-4-One
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Used in advanced organic synthesis as a chiral intermediate for pharmaceuticals, particularly in the development of steroid-like compounds and hormone analogs. Its complex stereochemistry makes it valuable for constructing biologically active molecules with high enantioselectivity. Commonly employed in research settings to design enzyme inhibitors and receptor modulators. The trimethylsilyl group acts as a protecting group, facilitating selective reactions in multi-step synthesis. Not typically used in i

Used in advanced organic synthesis as a chiral intermediate for pharmaceuticals, particularly in the development of steroid-like compounds and hormone analogs. Its complex stereochemistry makes it valuable for constructing biologically active molecules with high enantioselectivity. Commonly employed in research settings to design enzyme inhibitors and receptor modulators. The trimethylsilyl group acts as a protecting group, facilitating selective reactions in multi-step synthesis. Not typically used in industrial applications outside of specialized medicinal chemistry research.

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