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Structure of 14097-42-8
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2-Methyl-1,2,3,4-tetrahydroisoquinolin-5-ol delivers a rigid, electron-rich scaffold ideal for medicinal chemistry campaigns. This bench-stable heterocycle features a pendant hydroxyl group that enables direct derivatization or hydrogen bonding interactions in target binding sites. The methyl substitution enhances metabolic stability while maintaining favorable solubility profiles under standard conditions.
2-Methyl-1,2,3,4-tetrahydroisoquinolin-5-ol serves as a versatile heterocyclic building block for medicinal chemistry and natural product synthesis. Its phenolic hydroxyl group enables direct functionalization or derivatization, while the tetrahydroisoquinoline core provides structural rigidity and favorable pharmacophore properties. The molecule exhibits bench stability and compatibility with common protecting group strategies, facilitating downstream transformations in multistep syntheses.
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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: