N-(5-(tert-Butyl)isoxazol-3-yl)-2-chloroacetamide

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Reagent Code: #219879
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CAS Number 55809-27-3

science Other reagents with same CAS 55809-27-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.67 g/mol
Formula C₉H₁₃ClN₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides. Its structure allows for the introduction of isoxazole-based moieties, which are known for their biological activity in crop protection agents. It is also employed in the development of pharmaceutical candidates where the chloroacetamide group enables further functionalization through nucleophilic substitution. The tert-butyl group enhances lipophilicity, improving membrane permeability in bioactive molecules. Commonly utilized in research settings for designing novel compounds with enhanced stability and target specificity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿920.00
inventory 1g
10-20 days ฿2,990.00
inventory 5g
10-20 days ฿11,220.00

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N-(5-(tert-Butyl)isoxazol-3-yl)-2-chloroacetamide
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Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides. Its structure allows for the introduction of isoxazole-based moieties, which are known for their biological activity in crop protection agents. It is also employed in the development of pharmaceutical candidates where the chloroacetamide group enables further functionalization through nucleophilic substitution. The tert-butyl group enhances lipophilicity, improving membrane permeability in bioactive mo

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides. Its structure allows for the introduction of isoxazole-based moieties, which are known for their biological activity in crop protection agents. It is also employed in the development of pharmaceutical candidates where the chloroacetamide group enables further functionalization through nucleophilic substitution. The tert-butyl group enhances lipophilicity, improving membrane permeability in bioactive molecules. Commonly utilized in research settings for designing novel compounds with enhanced stability and target specificity.

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