Di-tert-butyl(methyl)silane

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Reagent Code: #178052
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CAS Number 56310-20-4

science Other reagents with same CAS 56310-20-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 158.36 g/mol
Formula C₉H₂₂Si
badge Registry Numbers
MDL Number MFCD00054890
thermostat Physical Properties
Boiling Point 155 °C
inventory_2 Storage & Handling
Density 0.758 g/cm3
Storage Room temperature, inert gas

description Product Description

Used as a silyl protecting group in organic synthesis, particularly for alcohols and phenols. The di-tert-butylmethylsilyl (DTBMS) group offers high stability under a variety of reaction conditions, including basic and mildly acidic environments, making it suitable for multi-step syntheses. It is more sterically hindered and more stable toward hydrolysis than smaller silyl groups like TMS or TBS, allowing selective deprotection in the presence of other silyl-protected functionalities. Commonly employed in the synthesis of complex natural products and pharmaceuticals where robust protection is required.

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inventory 25g
10-20 days ฿86,980.00

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Di-tert-butyl(methyl)silane
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Used as a silyl protecting group in organic synthesis, particularly for alcohols and phenols. The di-tert-butylmethylsilyl (DTBMS) group offers high stability under a variety of reaction conditions, including basic and mildly acidic environments, making it suitable for multi-step syntheses. It is more sterically hindered and more stable toward hydrolysis than smaller silyl groups like TMS or TBS, allowing selective deprotection in the presence of other silyl-protected functionalities. Commonly employed in t
Used as a silyl protecting group in organic synthesis, particularly for alcohols and phenols. The di-tert-butylmethylsilyl (DTBMS) group offers high stability under a variety of reaction conditions, including basic and mildly acidic environments, making it suitable for multi-step syntheses. It is more sterically hindered and more stable toward hydrolysis than smaller silyl groups like TMS or TBS, allowing selective deprotection in the presence of other silyl-protected functionalities. Commonly employed in the synthesis of complex natural products and pharmaceuticals where robust protection is required.
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