N-((tetrahydro-2H-pyran-2-yl)oxy)acrylamide

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Reagent Code: #218696
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CAS Number 1233211-05-6

science Other reagents with same CAS 1233211-05-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.09 g/mol
Formula C₈H₁₃NO₃
inventory_2 Storage & Handling
Storage Room temperature, airtight, dry

description Product Description

N-((tetrahydro-2H-pyran-2-yl)oxy)acrylamide is a specialty chemical intermediate used in organic synthesis for pharmaceuticals, natural products, and fine chemicals. It combines an acrylamide group, which enables addition and polymerization reactions, with a tetrahydro-2H-pyran-2-yl (THP) moiety that protects the N-hydroxy functionality. This protection stabilizes the molecule during multi-step reactions, allowing selective transformations at the acrylamide double bond or other sites. The THP group can be removed under mild acidic conditions to reveal the reactive N-hydroxyacrylamide, providing precise control in complex syntheses.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,650.00
inventory 1g
10-20 days ฿6,480.00
inventory 5g
10-20 days ฿19,440.00
N-((tetrahydro-2H-pyran-2-yl)oxy)acrylamide
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N-((tetrahydro-2H-pyran-2-yl)oxy)acrylamide is a specialty chemical intermediate used in organic synthesis for pharmaceuticals, natural products, and fine chemicals. It combines an acrylamide group, which enables addition and polymerization reactions, with a tetrahydro-2H-pyran-2-yl (THP) moiety that protects the N-hydroxy functionality. This protection stabilizes the molecule during multi-step reactions, allowing selective transformations at the acrylamide double bond or other sites. The THP group can b

N-((tetrahydro-2H-pyran-2-yl)oxy)acrylamide is a specialty chemical intermediate used in organic synthesis for pharmaceuticals, natural products, and fine chemicals. It combines an acrylamide group, which enables addition and polymerization reactions, with a tetrahydro-2H-pyran-2-yl (THP) moiety that protects the N-hydroxy functionality. This protection stabilizes the molecule during multi-step reactions, allowing selective transformations at the acrylamide double bond or other sites. The THP group can be removed under mild acidic conditions to reveal the reactive N-hydroxyacrylamide, providing precise control in complex syntheses.

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