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Structure of 30033-24-0
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(S)-2-((tert-Butoxycarbonyl)amino)-3-(3,4-dihydroxyphenyl)propanoic acid features a chiral center and a protected amine group, enabling its use in asymmetric synthesis. The catechol moiety offers strong metal-chelating capacity and redox activity. This bench-stable derivative serves as a key intermediate for bioactive molecule construction, particularly in dopamine-related pharmaceuticals and peptide conjugates.
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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 : P260-P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: