A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Safety of 5-Nitro-1H-indole-3-carbaldehyde, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 6625-96-3, Name is 5-Nitro-1H-indole-3-carbaldehyde, molecular formula is C9H6N2O3. In a Article, authors is Tang, Yingzhan，once mentioned of 6625-96-3
A highly useful and robust method to (heteroarylmethyl)phenols, derivatives of arylheteroarylmethanes, was developed based on iron(III)-catalyzed 1,3-rearrangement of (phenoxymethyl)heteroarenes. It features cheap catalyst, mild reaction conditions, short reaction time and broad substrate scope. The mechanism of reaction was supported by a crossover experiment. Its application was demonstrated by the synthesis of a key intermediate in the synthesis of an oral leukotriene receptor antagonist zafirlukast.
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Reference：
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles