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Structure of 1035700-06-1
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Methyl 1,2,3,4-tetrahydroisoquinoline-5-carboxylate hydrochloride delivers a stable, moisture-tolerant scaffold for medicinal chemistry campaigns. This bench-stable derivative integrates a polar carboxylate group with a rigid heterocyclic core, enabling direct functionalization at the C5 position. The protonated nitrogen enhances solubility in aqueous-organic mixtures while maintaining compatibility with standard coupling conditions.
Methyl 1,2,3,4-tetrahydroisoquinoline-5-carboxylate hydrochloride serves as a versatile building block for the synthesis of isoquinoline-based pharmaceuticals and bioactive heterocycles. The protected amine enables straightforward functionalization at the C5 position, while the ester group supports subsequent transformations such as hydrolysis, reduction, or coupling reactions. Its crystalline solid form ensures excellent bench stability and ease of handling, facilitating purification and scalability in medicinal chemistry workflows.
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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: