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Structure of 1663-61-2
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(Triethoxymethyl)benzene serves as a robust, bench-stable synthon for introducing triethoxymethyl groups into complex molecular architectures. This silicon-free reagent features orthogonal reactivity, enabling selective functionalization under mild conditions. The ethoxy substituents facilitate controlled hydrolysis and condensation, supporting efficient incorporation into polymers and surface-modified materials.
(Triethoxymethyl)benzene serves as a stable, bench-ready synthon for the introduction of benzyl-type C1 building blocks. Its triethoxymethyl group undergoes controlled hydrolysis to yield the corresponding aldehyde, enabling efficient aldol and Wittig reactions. The molecule exhibits excellent functional group tolerance and facilitates straightforward purification, making it a reliable reagent in complex molecule synthesis and heterocyclic scaffold construction.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: