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Structure of 220247-71-2
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This tetrahydroisoquinoline derivative features a carboxylic acid group at the 7-position, enabling direct conjugation or derivatization. The hydrochloride salt form enhances solubility and stability in aqueous systems, facilitating use in synthetic transformations and medicinal chemistry applications.
1,2,3,4-Tetrahydroisoquinoline-7-carboxylic acid hydrochloride serves as a versatile scaffold for medicinal chemistry and natural product synthesis. Its carboxylic acid functionality enables direct coupling reactions and derivatization under standard conditions. The hydrochloride salt enhances solubility and bench stability, facilitating purification and handling in multi-step syntheses. Functions as a key building block for heterocyclic systems and bioactive molecules requiring the tetrahydroisoquinoline core.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: