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Structure of 84100-84-5
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2,3,3-Trimethyl-3H-indole-5-carboxylic acid features a sterically hindered indole core with a carboxylic acid at the 5-position, enabling direct conjugation in bioconjugation workflows. The trimethyl substitution enhances solubility and metabolic stability, while the electron-rich indole scaffold supports efficient coupling under mild conditions. This derivative serves as a robust platform for developing fluorescent probes and targeted therapeutics.
2,3,3-Trimethyl-3H-indole-5-carboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling the construction of indole-based scaffolds with enhanced metabolic stability. Its carboxylic acid functionality facilitates direct coupling reactions and derivatization under standard conditions. The trimethyl substitution pattern confers improved bench stability and solubility in organic media, supporting efficient purification and scalability in medicinal chemistry campaigns.
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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-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: