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Structure of 2185014-88-2
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This chiral bis-oxazole scaffold features a rigid cyclohexylidene bridge that enforces defined spatial orientation, enabling precise molecular recognition. The dihydrooxazole rings provide stability and polarity, while the phenyl substituents enhance π-interactions. Ideal for asymmetric synthesis and catalyst design, this compound integrates seamlessly into complex architectures requiring controlled stereochemistry and robust handling under standard conditions.
(4S,4'S)-2,2'-Cyclohexylidenebis[4,5-dihydro-4-phenyloxazole] serves as a chiral bis-oxazole scaffold with defined stereochemistry at the 4 and 4' positions. It functions as a versatile building block in asymmetric synthesis, enabling controlled construction of complex heterocyclic architectures. The cyclohexylidene linker provides rigidity and enhances structural integrity, while the dihydrooxazole moieties offer functional group tolerance for downstream transformations. Its bench-stable nature and predictable reactivity facilitate integration into standard synthetic workflows for medicinal chemistry and catalytic system 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-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: