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Structure of 496-15-1
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N-(Aminooxy-PEG3)-N-bis(PEG4-t-butyl ester) is a branched aminooxy linker. It can react with aldehyde to form an oxime bond. If a reductant is used, it will form a hydroxylamine linkage. The t-butyl ester group can be hydrolyzed under acidic conditions. The hydrophilic PEG linkers increase the water solubility of the compound. Aminooxy compounds are very reactive and sensitive; they cannot be stored for long term. Immediate use (within 1 week) is highly recommended.
Indoline serves as a versatile heterocyclic building block in synthetic organic chemistry, enabling efficient access to biologically relevant scaffolds. Its saturated nitrogen-containing core exhibits favorable stability and functional group tolerance, facilitating diverse transformations including electrophilic substitution, metal-catalyzed coupling reactions, and reductive amination. Widely employed in medicinal chemistry, indoline functions as a key structural motif in kinase inhibitors and CNS-active compounds, offering predictable reactivity and straightforward purification in standard laboratory 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: