4-Methylsulphonylbenzoic acid

98%

Reagent Code: #205898
label
Alias p-methylsulfone benzoic acid; p-carboxyp-methylsulfone toluene; p-carboxyp-benzoic acid; 4-methylsulfonylbenzoic acid; 4-methylsulfonylbenzoic acid
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CAS Number 4052-30-6

science Other reagents with same CAS 4052-30-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.21 g/mol
Formula C₈H₈O₄S
badge Registry Numbers
MDL Number MFCD00007564
inventory_2 Storage & Handling
Storage Room temperature, sealed

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 in the development of compounds with analgesic and antipyretic properties. Also employed in the preparation of sulfonyl-containing bioactive molecules for medicinal research. Its functional groups allow for easy modification in organic synthesis, making it valuable in drug discovery and development processes.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿168.00
inventory 25g
10-20 days ฿440.00
inventory 100g
10-20 days ฿1,390.00
inventory 500g
10-20 days ฿6,550.00

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4-Methylsulphonylbenzoic 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 in the development of compounds with analgesic and antipyretic properties. Also employed in the preparation of sulfonyl-containing bioactive molecules for medicinal research. Its functional groups allow for easy modification in organic synthesis, making it valuable in drug discovery and development processes.

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 in the development of compounds with analgesic and antipyretic properties. Also employed in the preparation of sulfonyl-containing bioactive molecules for medicinal research. Its functional groups allow for easy modification in organic synthesis, making it valuable in drug discovery and development processes.

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