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Structure of 2412056-27-8
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Thalidomide-5-NH₂-CH₂-COOH integrates a strategically positioned amino-methylcarboxylate handle at the 5-position of the phthalimide core. This functionalized derivative enables direct conjugation in bioconjugation workflows, leveraging its reactive terminal amine and carboxylic acid for site-specific attachment. Designed for targeted drug delivery and probe development, it maintains the scaffold’s inherent stability and solubility profile under physiological conditions.
Thalidomide-5-NH₂-CH₂-COOH serves as a key functionalized intermediate for targeted derivatization in medicinal chemistry. The pendant amino and carboxyl groups enable facile conjugation and salt formation, enhancing solubility and enabling bioconjugate synthesis. Its stability under standard bench conditions supports reliable handling, while the preserved glutarimide core maintains intrinsic activity relevant to immunomodulatory and anti-angiogenic applications.
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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: