2-(2,6-Dichlorophenyl)acetamide

97%

Reagent Code: #177484
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CAS Number 78433-88-2

science Other reagents with same CAS 78433-88-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.05 g/mol
Formula C₈H₇Cl₂NO
badge Registry Numbers
MDL Number MFCD00082745
thermostat Physical Properties
Melting Point 216-218 °C
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of anti-inflammatory and analgesic agents. It serves as a key building block in the development of phenylacetic acid derivatives, which are structurally related to nonsteroidal anti-inflammatory drugs (NSAIDs). Its chlorinated aromatic structure enhances its reactivity and selectivity in various coupling and substitution reactions, making it valuable in medicinal chemistry for optimizing drug potency and metabolic stability. Additionally, it has been explored in agrochemical research for the design of bioactive molecules with potential pesticidal or herbicidal activity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿610.00
inventory 1g
10-20 days ฿1,240.00
inventory 5g
10-20 days ฿5,450.00
inventory 25g
10-20 days ฿19,510.00

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2-(2,6-Dichlorophenyl)acetamide
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Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of anti-inflammatory and analgesic agents. It serves as a key building block in the development of phenylacetic acid derivatives, which are structurally related to nonsteroidal anti-inflammatory drugs (NSAIDs). Its chlorinated aromatic structure enhances its reactivity and selectivity in various coupling and substitution reactions, making it valuable in medicinal chemistry for optimizing drug potency and

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of anti-inflammatory and analgesic agents. It serves as a key building block in the development of phenylacetic acid derivatives, which are structurally related to nonsteroidal anti-inflammatory drugs (NSAIDs). Its chlorinated aromatic structure enhances its reactivity and selectivity in various coupling and substitution reactions, making it valuable in medicinal chemistry for optimizing drug potency and metabolic stability. Additionally, it has been explored in agrochemical research for the design of bioactive molecules with potential pesticidal or herbicidal activity.

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