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Structure of 1251471-84-7
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This chiral acetonitrile derivative features two sterically encumbered oxazoline rings that confer exceptional stability and selective coordination. The (S)-configured dihydrooxazolyl groups enable precise stereocontrol in asymmetric synthesis, while the nitrile functionality offers versatile coupling potential. Designed for use in catalytic systems requiring rigid, electron-deficient ligands, this compound streamlines access to enantioselective transformations under standard bench conditions.
2,2-Bis((S)-4-(tert-butyl)-4,5-dihydrooxazol-2-yl)acetonitrile serves as a chiral, bench-stable synthon for asymmetric synthesis, enabling the construction of complex heterocyclic scaffolds through controlled C–C and C–N bond formations. Its dual oxazoline functionality provides orthogonal reactivity, facilitates purification via crystallization, and supports functional group tolerance in standard coupling protocols.
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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-P271-P280-P302+P352-P405-P501
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Lot numbers can be found on the outside label of a product: