N-(2-(Allyloxy)benzyl)-N-(benzo[d][1,3]dioxol-5-yl)-2-chloroacetamide

95%

Reagent Code: #219916
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CAS Number 851452-58-9

science Other reagents with same CAS 851452-58-9

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Storage 2-8°C, Inert Gas

description Product Description

Used primarily in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Its structure supports the development of agents targeting central nervous system disorders due to the presence of the benzodioxole moiety, which is known for interacting with neurological receptors. The chloroacetamide group allows for further functionalization, making it valuable in constructing complex molecules. It is also employed in the preparation of enzyme inhibitors and receptor ligands in medicinal chemistry research. Additionally, the allyloxy group enables selective deprotection or cross-coupling reactions, enhancing its utility in multi-step synthetic routes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿850.00
inventory 250mg
10-20 days ฿1,770.00
inventory 1g
10-20 days ฿6,280.00

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N-(2-(Allyloxy)benzyl)-N-(benzo[d][1,3]dioxol-5-yl)-2-chloroacetamide
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Used primarily in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Its structure supports the development of agents targeting central nervous system disorders due to the presence of the benzodioxole moiety, which is known for interacting with neurological receptors. The chloroacetamide group allows for further functionalization, making it valuable in constructing complex molecules. It is also employed in the preparation of enzyme inhibitors and receptor ligands

Used primarily in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Its structure supports the development of agents targeting central nervous system disorders due to the presence of the benzodioxole moiety, which is known for interacting with neurological receptors. The chloroacetamide group allows for further functionalization, making it valuable in constructing complex molecules. It is also employed in the preparation of enzyme inhibitors and receptor ligands in medicinal chemistry research. Additionally, the allyloxy group enables selective deprotection or cross-coupling reactions, enhancing its utility in multi-step synthetic routes.

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