4-(Chlorosulfonyl)benzoicacid

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Reagent Code: #159430
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CAS Number 10130-89-9

science Other reagents with same CAS 10130-89-9

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Weight 220.63 g/mol
Formula C₇H₅ClO₄S
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MDL Number MFCD00007448
inventory_2 Storage & Handling
Storage Room temperature

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Used primarily as an intermediate in organic synthesis, this compound plays a key role in the preparation of sulfa drugs and other pharmaceuticals. Its reactive sulfonyl chloride group allows it to form sulfonamides when reacted with amines, a critical step in creating antibiotics like sulfonamide-based antimicrobials. It is also employed in the synthesis of dyes, agrochemicals, and functional polymers due to its ability to introduce sulfonic acid derivatives into complex molecules. In research, it serves as a building block for modifying aromatic structures and developing new bioactive compounds.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿310.00
inventory 5g
10-20 days ฿1,300.00
inventory 25g
10-20 days ฿4,750.00

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4-(Chlorosulfonyl)benzoicacid
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Used primarily as an intermediate in organic synthesis, this compound plays a key role in the preparation of sulfa drugs and other pharmaceuticals. Its reactive sulfonyl chloride group allows it to form sulfonamides when reacted with amines, a critical step in creating antibiotics like sulfonamide-based antimicrobials. It is also employed in the synthesis of dyes, agrochemicals, and functional polymers due to its ability to introduce sulfonic acid derivatives into complex molecules. In research, it serve

Used primarily as an intermediate in organic synthesis, this compound plays a key role in the preparation of sulfa drugs and other pharmaceuticals. Its reactive sulfonyl chloride group allows it to form sulfonamides when reacted with amines, a critical step in creating antibiotics like sulfonamide-based antimicrobials. It is also employed in the synthesis of dyes, agrochemicals, and functional polymers due to its ability to introduce sulfonic acid derivatives into complex molecules. In research, it serves as a building block for modifying aromatic structures and developing new bioactive compounds.

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