(E)-2-((3S,5R)-3,5-Bis((tert-butyldimethylsilyl)oxy)-2-methylenecyclohexylidene)ethan-1-ol

98%

Reagent Code: #180605
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CAS Number 227961-42-4

science Other reagents with same CAS 227961-42-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 398.73 g/mol
Formula C₂₁H₄₂O₃Si₂
badge Registry Numbers
MDL Number MFCD32857246
thermostat Physical Properties
Boiling Point 411.4±45.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of vitamin D analogs and related steroidal compounds. Its functionalized cyclohexylidene backbone with protected hydroxyl groups allows selective deprotection and further chemical modifications, making it valuable in pharmaceutical research, particularly in developing drugs targeting metabolic and hormonal disorders. The silyl protecting groups enhance stability and solubility during multi-step syntheses, while the exocyclic methylene and alkene alcohol moieties enable coupling reactions and ring transformations essential for constructing complex steroid-like structures.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿2,480.00
inventory 10mg
10-20 days ฿12,950.00

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(E)-2-((3S,5R)-3,5-Bis((tert-butyldimethylsilyl)oxy)-2-methylenecyclohexylidene)ethan-1-ol
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Used as a key intermediate in the synthesis of vitamin D analogs and related steroidal compounds. Its functionalized cyclohexylidene backbone with protected hydroxyl groups allows selective deprotection and further chemical modifications, making it valuable in pharmaceutical research, particularly in developing drugs targeting metabolic and hormonal disorders. The silyl protecting groups enhance stability and solubility during multi-step syntheses, while the exocyclic methylene and alkene alcohol moieties e
Used as a key intermediate in the synthesis of vitamin D analogs and related steroidal compounds. Its functionalized cyclohexylidene backbone with protected hydroxyl groups allows selective deprotection and further chemical modifications, making it valuable in pharmaceutical research, particularly in developing drugs targeting metabolic and hormonal disorders. The silyl protecting groups enhance stability and solubility during multi-step syntheses, while the exocyclic methylene and alkene alcohol moieties enable coupling reactions and ring transformations essential for constructing complex steroid-like structures.
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