2-Bromo-N-(4-ethoxyphenyl)acetamide

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Reagent Code: #141367
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CAS Number 34325-71-8

science Other reagents with same CAS 34325-71-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.12 g/mol
Formula C₁₀H₁₂BrNO₂
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MDL Number MFCD02974373
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It serves in the development of bioactive molecules due to the presence of both bromo and amide functional groups, which allow for further chemical modifications. Commonly employed in the synthesis of substituted anilides and heterocyclic compounds with potential antimicrobial or anti-inflammatory activity. Also utilized in research settings for the construction of more complex drug-like molecules through nucleophilic substitution or palladium-catalyzed coupling reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,250.00
inventory 250mg
10-20 days ฿5,490.00
inventory 1g
10-20 days ฿14,830.00

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2-Bromo-N-(4-ethoxyphenyl)acetamide
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It serves in the development of bioactive molecules due to the presence of both bromo and amide functional groups, which allow for further chemical modifications. Commonly employed in the synthesis of substituted anilides and heterocyclic compounds with potential antimicrobial or anti-inflammatory activity. Also utilized in research settings for the construction of more complex drug-like molecules t

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It serves in the development of bioactive molecules due to the presence of both bromo and amide functional groups, which allow for further chemical modifications. Commonly employed in the synthesis of substituted anilides and heterocyclic compounds with potential antimicrobial or anti-inflammatory activity. Also utilized in research settings for the construction of more complex drug-like molecules through nucleophilic substitution or palladium-catalyzed coupling reactions.

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