N-(2-Acetylphenyl)-2-chloroacetamide

98%

Reagent Code: #220384
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CAS Number 6140-11-0

science Other reagents with same CAS 6140-11-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.64 g/mol
Formula C₁₀H₁₀ClNO₂
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MDL Number MFCD03092700
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds. It plays a role in the development of pharmaceuticals due to its ability to participate in cyclization reactions that form bioactive molecule scaffolds. Commonly employed in the synthesis of indole and oxazole derivatives, which exhibit antimicrobial, anti-inflammatory, and anticancer activities. Also utilized in agrochemical research for designing novel pesticide agents owing to its reactivity with nucleophiles and stability under various reaction conditions.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,200.00

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N-(2-Acetylphenyl)-2-chloroacetamide
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Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds. It plays a role in the development of pharmaceuticals due to its ability to participate in cyclization reactions that form bioactive molecule scaffolds. Commonly employed in the synthesis of indole and oxazole derivatives, which exhibit antimicrobial, anti-inflammatory, and anticancer activities. Also utilized in agrochemical research for designing novel pesticide agents owing to its reactivity with n

Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds. It plays a role in the development of pharmaceuticals due to its ability to participate in cyclization reactions that form bioactive molecule scaffolds. Commonly employed in the synthesis of indole and oxazole derivatives, which exhibit antimicrobial, anti-inflammatory, and anticancer activities. Also utilized in agrochemical research for designing novel pesticide agents owing to its reactivity with nucleophiles and stability under various reaction conditions.

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