Sodium 4-formylbenzene-1,3-disulfonate, commonly known as $name$, serves as a crucial reagent in chemical synthesis, particularly in the realm of organic chemistry. This compound plays a pivotal role in the construction of various complex organic molecules, owing to its unique structural properties and reactivity.One of the primary applications of $name$ lies in its utility as a versatile carbonylating agent. By introducing a formyl group into organic molecules through the use of $name$, chemists can functionalize a wide range of substrates, leading to the synthesis of diverse organic compounds with formyl moieties. This formyl group serves as a key functional group in numerous organic reactions and can subsequently undergo various transformations to yield valuable intermediates or final products.Moreover, the sulfonate groups present in the molecular structure of $name$ provide additional avenues for chemical modification and derivatization. These sulfonate groups can participate in various sulfonation reactions, enabling the introduction of additional functional groups onto organic molecules. This capability further enhances the synthetic utility of $name$ in the preparation of complex organic frameworks.Furthermore, the presence of the benzene ring in $name$ imparts aromatic character to the molecule, thereby influencing its reactivity and participation in aromatic substitution reactions. This feature expands the synthetic versatility of $name$ in an array of transformations, allowing chemists to access diverse chemical spaces and achieve desired structural motifs in the target molecules.Overall, the strategic incorporation of Sodium 4-formylbenzene-1,3-disulfonate, or $name$, in chemical synthesis processes underscores its significance as a valuable building block for the construction of complex organic compounds with tailored functionalities, highlighting its role as a versatile reagent in the hands of synthetic chemists.
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