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Structure of 851477-19-5
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N-[3,5-Bis(trifluoromethyl)phenyl]-N'-(9R)-cinchonan-9-ylthiourea features a chiral cinchona scaffold paired with electron-deficient aryl thiourea functionality, enabling precise asymmetric catalysis. The trifluoromethyl groups enhance lipophilicity and stabilize transition states in enantioselective transformations. This bifunctional architecture supports efficient hydrogen-bonding networks and delivers high enantiomeric excesses in metal-free organocatalytic reactions under standard conditions.
N-[3,5-Bis(trifluoromethyl)phenyl]-N'-(9R)-cinchonan-9-ylthiourea serves as a chiral bifunctional catalyst in asymmetric synthesis, leveraging the rigid cinchona alkaloid scaffold for stereocontrol. The thiourea moiety engages in hydrogen bonding with substrates, while the electron-deficient aryl group enhances electrophile activation. Its bench-stable nature and compatibility with common solvents facilitate reliable operation in enantioselective transformations, particularly in Michael additions and Mannich reactions.
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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 : H413
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Precautionary Statements : P264-P270-P330
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Lot numbers can be found on the outside label of a product: