2-acetyloxy-5-chlorobenzoic acid

97%

Reagent Code: #129226
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CAS Number 1734-62-9

science Other reagents with same CAS 1734-62-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.6 g/mol
Formula C₉H₇ClO₄
badge Registry Numbers
MDL Number MFCD00096360
thermostat Physical Properties
Melting Point 148 °C
Boiling Point 348.7±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.416±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as an intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of diclofenac. It serves as a key building block due to the presence of both carboxylic acid and acetylated phenolic functionalities, enabling selective chemical modifications. Its chlorinated aromatic structure facilitates further substitution reactions, making it valuable in pharmaceutical manufacturing. Also employed in the development of derivatives for biological activity screening in medicinal chemistry research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,870.00
inventory 1g
10-20 days ฿7,920.00
2-acetyloxy-5-chlorobenzoic acid
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Used primarily as an intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of diclofenac. It serves as a key building block due to the presence of both carboxylic acid and acetylated phenolic functionalities, enabling selective chemical modifications. Its chlorinated aromatic structure facilitates further substitution reactions, making it valuable in pharmaceutical manufacturing. Also employed in the development of derivatives for biological activ

Used primarily as an intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of diclofenac. It serves as a key building block due to the presence of both carboxylic acid and acetylated phenolic functionalities, enabling selective chemical modifications. Its chlorinated aromatic structure facilitates further substitution reactions, making it valuable in pharmaceutical manufacturing. Also employed in the development of derivatives for biological activity screening in medicinal chemistry research.

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