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Structure of 106904-09-0
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This benzoic acid derivative features a methylsulfonyl group enhancing solubility and stability, paired with a chloro substituent enabling downstream functionalization. The methylated ring system imparts steric control, making it ideal for constructing bioactive scaffolds in medicinal chemistry and materials synthesis under standard conditions.
2-Chloro-3-methyl-4-(methylsulfonyl)benzoic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles and pharmaceutical intermediates. Its ortho-chloro and methylsulfonyl groups provide enhanced electrophilicity and metabolic stability, while the carboxylic acid functionality facilitates direct coupling reactions. The compound exhibits excellent bench stability and compatibility with standard amide, ester, and Suzuki coupling protocols, making it well-suited for iterative synthetic strategies in API development.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: