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Structure of 6279-86-3
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Triethyl methanetricarboxylate features three ester groups flanking a central carbon, enabling efficient multicomponent reactions. This electron-deficient triester integrates readily into synthetic sequences, offering high reactivity under mild conditions. The molecule's symmetry and steric profile support clean functionalization, making it ideal for constructing complex carbocycles and heterocycles in medicinal chemistry workflows.
Triethyl methanetricarboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of substituted malonate derivatives and heterocyclic scaffolds. Its three ester groups provide orthogonal reactivity for sequential functionalization, while the central methylene unit offers high nucleophilicity for alkylation and condensation reactions. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for multi-step syntheses in medicinal chemistry and process development workflows.
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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-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: