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Structure of 127168-90-5
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Methyl isoindoline-4-carboxylate hydrochloride delivers a stable, moisture-tolerant scaffold for synthetic applications. This bench-stable derivative features a protonated nitrogen that enhances solubility and reactivity in polar media. Its electron-rich isoindoline core facilitates coupling reactions under mild conditions, enabling efficient integration into complex molecular architectures.
Methyl isoindoline-4-carboxylate hydrochloride serves as a versatile building block for heterocyclic synthesis, enabling efficient access to isoindoline-based scaffolds prevalent in medicinal chemistry. Its bench-stable nature and compatibility with standard coupling reactions facilitate straightforward functionalization. The carboxylate group supports derivatization via ester manipulation, while the protonated nitrogen enhances solubility and reactivity in polar media, making it well-suited for iterative synthetic sequences.
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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: