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Structure of 14446-24-3
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1,2,3,4-Tetrahydro-6-isoquinolinol features a saturated isoquinoline core with a hydroxyl group at the 6-position, offering enhanced solubility and stability compared to aromatic analogs. This scaffold integrates readily into bioactive molecule design, particularly in CNS-targeted compounds, due to its favorable polarity and metabolic resilience under standard bench conditions.
1,2,3,4-Tetrahydro-6-isoquinolinol serves as a versatile scaffold for the synthesis of isoquinoline-based pharmaceuticals and bioactive molecules. Its saturated ring system offers enhanced stability and favorable solubility, while the primary alcohol functionality enables straightforward derivatization via esterification, etherification, or coupling reactions. This compound functions as a key intermediate in the construction of heterocyclic frameworks relevant to medicinal chemistry and natural product synthesis.
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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: