4-Acetyl-2-chloro-benzoic acid

95%

Reagent Code: #137860
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CAS Number 115382-35-9

science Other reagents with same CAS 115382-35-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.60 g/mol
Formula C₉H₇ClO₃
badge Registry Numbers
MDL Number MFCD20639602
thermostat Physical Properties
Melting Point 228 °C
Boiling Point 375.6±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.365±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs). It serves as a building block for introducing acetyl and carboxylic acid functionalities in drug molecules. Also employed in the development of agrochemicals and specialty organic compounds where chlorinated aromatic structures are required. Its reactivity allows for further functionalization through esterification, amidation, and halogen displacement reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,300.00
inventory 250mg
10-20 days ฿2,150.00
inventory 1g
10-20 days ฿6,950.00

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4-Acetyl-2-chloro-benzoic acid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs). It serves as a building block for introducing acetyl and carboxylic acid functionalities in drug molecules. Also employed in the development of agrochemicals and specialty organic compounds where chlorinated aromatic structures are required. Its reactivity allows for further functionalization through esterification, amidation, and halogen displacement reactions.
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs). It serves as a building block for introducing acetyl and carboxylic acid functionalities in drug molecules. Also employed in the development of agrochemicals and specialty organic compounds where chlorinated aromatic structures are required. Its reactivity allows for further functionalization through esterification, amidation, and halogen displacement reactions.
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