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Structure of 24370-74-9
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6-(Benzyloxy)-1H-indole-3-carboxylic acid integrates a benzyl ether-functionalized indole core with a carboxylic acid handle, enabling direct conjugation in peptide synthesis and medicinal chemistry. The benzyloxy group enhances solubility and stability under standard conditions, while the electron-deficient indole ring facilitates electrophilic substitution reactions. This scaffold serves as a key building block for bioactive molecule development.
6-(Benzyloxy)-1H-indole-3-carboxylic acid serves as a versatile building block for indole-based pharmaceutical scaffolds, enabling direct functionalization at the C6 position via orthogonal deprotection. The benzyloxy group provides excellent bench stability and can be selectively removed under mild hydrogenolysis conditions, facilitating downstream derivatization. The carboxylic acid functionality supports standard coupling reactions with amines, alcohols, and nucleophiles, making it ideal for constructing bioactive heterocycles and peptide conjugates in medicinal chemistry 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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: