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Structure of 1361563-40-7
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This bis-oxazolyl-substituted isoindole features a rigid, electron-deficient core enabling precise coordination in transition metal catalysis. The (1Z,3Z)-configuration ensures optimal spatial alignment for chelation, while the dihydrooxazolyl moieties enhance stability and solubility under standard reaction conditions.
(1Z,3Z)-1,3-Bis[[(4S)-4,5-dihydro-4-isopropyl-2-oxazolyl]methylene]-2,3-dihydro-1H-isoindole serves as a versatile bis-electrophilic scaffold for the construction of complex heterocyclic architectures. Its conjugated diene system enables Diels-Alder cycloadditions with high regioselectivity, while the oxazolyl substituents offer orthogonal reactivity for downstream functionalization. The molecule exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for modular synthesis in medicinal chemistry and materials science applications.
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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: