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Structure of 6270-06-0
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2-(2-Chloroethyl)isoindoline-1,3-dione features a reactive chloroethyl handle that enables site-specific conjugation in bioconjugation workflows. The isoindoline-1,3-dione core provides enhanced stability and solubility in aqueous and organic media. This compound integrates readily into peptide and protein modification protocols under mild conditions.
2-(2-Chloroethyl)isoindoline-1,3-dione serves as a versatile bifunctional building block in synthetic organic chemistry, combining a reactive chloroalkyl handle with a stable phthalimide scaffold. It facilitates efficient nucleophilic substitution reactions, enabling the introduction of diverse amine- and thiol-containing functionalities. The compound exhibits excellent bench stability and ease of purification, making it well-suited for iterative synthesis, peptide conjugation, and the construction of heterocyclic scaffolds 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: