(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%

Reagent Code: #231606
fingerprint
CAS Number 140710-96-9

science Other reagents with same CAS 140710-96-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 645.16 g/mol
Formula C₃₉H₇₂O₃Si₂
inventory_2 Storage & Handling
Storage Room temperature

description 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.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿38,610.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(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
No image available
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.
Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...