4-((Tert-Butyldiphenylsilyl)Oxy)-2,2-Dimethylbutan-1-Ol

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Reagent Code: #242764
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CAS Number 439693-30-8

science Other reagents with same CAS 439693-30-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 356.6 g/mol
Formula C₂₂H₃₂O₂Si
badge Registry Numbers
MDL Number MFCD28991835
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of complex natural products and pharmaceuticals. Its primary role is as a protected diol building block, where the silyl ether group provides stability under various reaction conditions while allowing selective deprotection when needed. Commonly employed in multi-step syntheses of bioactive molecules, including antibiotics and antiviral agents, due to its compatibility with a wide range of functional groups and its ability to control stereochemistry during coupling reactions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿21,480.00
inventory 1g
10-20 days ฿42,980.00

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4-((Tert-Butyldiphenylsilyl)Oxy)-2,2-Dimethylbutan-1-Ol
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Used as a key intermediate in organic synthesis, particularly in the preparation of complex natural products and pharmaceuticals. Its primary role is as a protected diol building block, where the silyl ether group provides stability under various reaction conditions while allowing selective deprotection when needed. Commonly employed in multi-step syntheses of bioactive molecules, including antibiotics and antiviral agents, due to its compatibility with a wide range of functional groups and its ability t

Used as a key intermediate in organic synthesis, particularly in the preparation of complex natural products and pharmaceuticals. Its primary role is as a protected diol building block, where the silyl ether group provides stability under various reaction conditions while allowing selective deprotection when needed. Commonly employed in multi-step syntheses of bioactive molecules, including antibiotics and antiviral agents, due to its compatibility with a wide range of functional groups and its ability to control stereochemistry during coupling reactions.

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