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Structure of 1256245-79-0
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This cyclobutenedione features a 3,5-bis(trifluoromethyl)phenylamino group and a (9R)-6'-methoxycinchonan-9-ylamino substituent, combining electron-deficient aromatic character with a chiral quinoline scaffold. The structure integrates a sterically defined bridge enabling precise spatial control in asymmetric synthesis applications.
3-[[3,5-Bis(trifluoromethyl)phenyl]amino]-4-[[(9R)-6'-methoxycinchonan-9-yl]amino]-3-cyclobutene-1,2-dione serves as a versatile scaffold for asymmetric catalysis and medicinal chemistry applications. Its conjugated quinone core enables robust Diels-Alder reactivity, while the chiral cinchona moiety provides stereocontrol in enantioselective transformations. Bench-stable and compatible with diverse functional groups, it facilitates efficient synthesis of complex heterocyclic systems and drug-like scaffolds under standard laboratory conditions.
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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: