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Structure of 14097-40-6
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2-Methyl-1,2,3,4-tetrahydroisoquinolin-7-amine features a sterically hindered tetrahydroisoquinoline core with a primary amine at the 7-position, enabling direct functionalization in synthetic routes. This scaffold integrates readily into bioactive molecules, offering enhanced metabolic stability and favorable solubility for medicinal chemistry applications.
2-Methyl-1,2,3,4-tetrahydroisoquinolin-7-amine serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive alkaloids and heterocyclic scaffolds. Its pendant amine group facilitates facile functionalization, while the tetrahydroisoquinoline core exhibits favorable stability and solubility for solution-phase synthesis. The molecule functions effectively in reductive amination, coupling reactions, and cyclization protocols commonly employed in API development.
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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-P405-P501
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Lot numbers can be found on the outside label of a product: