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Structure of 20289-26-3
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4-Benzyloxyindole integrates a benzyl ether moiety at the 4-position of the indole scaffold, enhancing solubility and stability in organic synthesis. This derivative serves as a key intermediate in the development of bioactive heterocycles, particularly in medicinal chemistry applications involving indole-based scaffolds.
4-Benzyloxyindole serves as a versatile building block in medicinal chemistry, enabling efficient access to indole-based scaffolds through mild deprotection under hydrogenolysis conditions. The benzyloxy group provides excellent stability during standard synthetic manipulations and exhibits high functional group tolerance, facilitating downstream derivatization at the indole nitrogen or C3 position. Its bench-stable nature and compatibility with common coupling reactions make it a practical choice for the synthesis of bioactive heterocycles and API intermediates.
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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
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Lot numbers can be found on the outside label of a product: