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Structure of 1872262-74-2
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This tetrahydro-2H-pyran-4-carboxylate integrates a reactive isoindoline scaffold with a stable, moisture-tolerant pyran ring. The dihydroisoindole core enables efficient coupling in synthetic sequences, while the protected carboxylate facilitates selective derivatization under mild conditions.
1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl tetrahydro-2H-pyran-4-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of complex heterocyclic scaffolds. Its fused isoindoline core and protected carboxylic acid functionality offer enhanced bench stability and compatibility with standard coupling reactions. The molecule facilitates orthogonal functional group manipulation and is particularly valuable in the synthesis of bioactive compounds requiring precise stereochemical control and structural rigidity.
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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-P405-P501
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Lot numbers can be found on the outside label of a product: