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Structure of 933752-32-0
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1,2,3,4-Tetrahydroisoquinoline-6-carboxylic acid features a rigid, electron-rich heterocyclic core paired with a carboxylic acid handle, enabling direct integration into peptide mimetics and bioactive scaffolds. This bench-stable derivative supports diverse synthetic transformations under standard conditions.
1,2,3,4-Tetrahydroisoquinoline-6-carboxylic acid serves as a versatile scaffold in medicinal chemistry, enabling the synthesis of bioactive heterocycles through established coupling and functionalization reactions. Its carboxylic acid group facilitates amide bond formation, while the tetrahydroisoquinoline core provides structural rigidity and favorable pharmacophoric properties. The compound exhibits good bench stability and compatibility with standard purification techniques, making it suitable for iterative synthetic campaigns targeting CNS-active compounds and kinase inhibitors.
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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
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Precautionary Statements : P264-P270-P301+P310-P330-P501
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Lot numbers can be found on the outside label of a product: