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Structure of 30250-67-0
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This bench-stable isoindoline-1,3-dione derivative features a pendant aminoethyl side chain, enabling facile conjugation in bioconjugation workflows. The hydrochloride salt enhances solubility in aqueous media, supporting efficient incorporation into peptide and protein labeling strategies under standard conditions.
2-(2-Aminoethyl)isoindoline-1,3-dione hydrochloride serves as a versatile scaffold for heterocyclic synthesis, enabling efficient access to bioactive molecules through amine-directed functionalization. Its bench-stable hydrochloride salt form enhances handling and solubility, while the pendant primary amine facilitates conjugation reactions and derivatization under mild conditions. Functions effectively in peptide coupling, reductive amination, and transition-metal-catalyzed transformations, making it a practical building block for medicinal chemistry campaigns targeting CNS agents and kinase inhibitors.
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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+P364-P405-P501
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Lot numbers can be found on the outside label of a product: