2-Chloro-N-(2,4-dimethoxyphenyl)acetamide

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Reagent Code: #163617
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CAS Number 101908-41-2

science Other reagents with same CAS 101908-41-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.66 g/mol
Formula C₁₀H₁₂ClNO₃
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MDL Number MFCD00750873
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antitumor and antimicrobial agents. It serves as a building block in organic reactions where the chloroacetamide group is utilized for nucleophilic substitution, enabling the formation of amide or ether linkages. Its electron-donating methoxy groups enhance reactivity in electrophilic aromatic substitution, making it valuable in the preparation of more complex bioactive molecules. Commonly employed in research settings for designing kinase inhibitors and other therapeutic agents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,350.00
inventory 1g
10-20 days ฿6,700.00
inventory 100mg
10-20 days ฿1,830.00

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2-Chloro-N-(2,4-dimethoxyphenyl)acetamide
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antitumor and antimicrobial agents. It serves as a building block in organic reactions where the chloroacetamide group is utilized for nucleophilic substitution, enabling the formation of amide or ether linkages. Its electron-donating methoxy groups enhance reactivity in electrophilic aromatic substitution, making it valuable in the preparation of more complex bioactive molecules. Commonly employed in research

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antitumor and antimicrobial agents. It serves as a building block in organic reactions where the chloroacetamide group is utilized for nucleophilic substitution, enabling the formation of amide or ether linkages. Its electron-donating methoxy groups enhance reactivity in electrophilic aromatic substitution, making it valuable in the preparation of more complex bioactive molecules. Commonly employed in research settings for designing kinase inhibitors and other therapeutic agents.

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