2-((tert-Butyldiphenylsilyl)oxy)-N-methoxy-N-methylacetamide

≥95%

Reagent Code: #41168
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CAS Number 154698-93-8

science Other reagents with same CAS 154698-93-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 357.52 g/mol
Formula C₂₀H₂₇NO₃Si
badge Registry Numbers
MDL Number MFCD14585077
thermostat Physical Properties
Boiling Point 395°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

2-((tert-Butyldiphenylsilyl)oxy)-N-methoxy-N-methylacetamide is a specialty chemical intermediate, specifically a protected Weinreb amide derivative of glycolic acid. It is used in organic synthesis to introduce alpha-oxygenated carbonyl functionalities. The tert-butyldiphenylsilyl (TBDPS) protecting group shields the hydroxyl moiety, enabling selective manipulation of the Weinreb amide, which reacts with organometallic reagents to form ketones. This compound is valuable in multi-step syntheses of complex molecules, including pharmaceuticals and natural products, due to its stability and orthogonality in deprotection strategies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,484.00
inventory 250mg
10-20 days ฿3,960.00

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2-((tert-Butyldiphenylsilyl)oxy)-N-methoxy-N-methylacetamide
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2-((tert-Butyldiphenylsilyl)oxy)-N-methoxy-N-methylacetamide is a specialty chemical intermediate, specifically a protected Weinreb amide derivative of glycolic acid. It is used in organic synthesis to introduce alpha-oxygenated carbonyl functionalities. The tert-butyldiphenylsilyl (TBDPS) protecting group shields the hydroxyl moiety, enabling selective manipulation of the Weinreb amide, which reacts with organometallic reagents to form ketones. This compound is valuable in multi-step syntheses of complex m
2-((tert-Butyldiphenylsilyl)oxy)-N-methoxy-N-methylacetamide is a specialty chemical intermediate, specifically a protected Weinreb amide derivative of glycolic acid. It is used in organic synthesis to introduce alpha-oxygenated carbonyl functionalities. The tert-butyldiphenylsilyl (TBDPS) protecting group shields the hydroxyl moiety, enabling selective manipulation of the Weinreb amide, which reacts with organometallic reagents to form ketones. This compound is valuable in multi-step syntheses of complex molecules, including pharmaceuticals and natural products, due to its stability and orthogonality in deprotection strategies.
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