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Structure of 1020665-73-9
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This sulfonamide features a sterically hindered cyclohexyl amine scaffold paired with electron-deficient trifluoromethyl aryl groups, enabling selective binding in kinase inhibition studies. The dimethylamino functionality enhances solubility and metabolic stability under standard bench conditions.
N-[(1R,2R)-2-[[[[(1R,2R)-2-(Dimethylamino)cyclohexyl]amino]thioxomethyl]amino]-1,2-diphenylethyl]-3,5-bis(trifluoromethyl)benzenesulfonamide serves as a versatile bifunctional building block in medicinal chemistry, enabling the construction of complex chiral scaffolds. Its thioxoamide functionality facilitates amide bond formation and transition metal-catalyzed coupling reactions, while the trifluoromethyl-substituted sulfonamide enhances metabolic stability and membrane permeability. The rigid diphenylethyl moiety provides conformational constraint, and the dimethylaminocyclohexyl group offers favorable solubility and handling characteristics for iterative synthesis workflows.
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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: