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Structure of 1003886-05-2
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This chiral bis-oxazole scaffold features a rigid cyclopentylidene bridge that enforces defined spatial orientation, enabling precise molecular recognition. The phenylmethyl-substituted oxazole rings provide enhanced solubility and stability under standard bench conditions, while the (4S,4'S) stereochemistry ensures high diastereoselectivity in asymmetric synthesis applications.
(4S,4'S)-2,2'-Cyclopentylidenebis[4,5-dihydro-4-(phenylmethyl)oxazole] serves as a chiral bis-oxazole scaffold with defined stereochemistry at the cyclopentylidene bridge. It functions as a versatile building block in asymmetric synthesis, enabling the construction of complex heterocyclic systems through controlled functionalization. The molecule exhibits excellent bench stability and facilitates orthogonal reactivity due to the protected oxazole rings and well-defined stereogenic centers, supporting efficient downstream transformations in medicinal chemistry and catalyst design.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: