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Structure of 421551-75-9
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tert-Butyl(4-formylphenethyl)carbamate features a benzaldehyde handle tethered to a robust tert-butyl carbamate group, enabling seamless incorporation into diverse synthetic scaffolds. This bench-stable reagent facilitates efficient derivatization workflows under standard conditions.
tert-Butyl(4-formylphenethyl)carbamate serves as a versatile building block in medicinal chemistry, enabling efficient access to bioactive scaffolds via standard functional group transformations. The aldehyde functionality facilitates reductive amination, Wittig reactions, and conjugate additions, while the tert-butyl carbamate group offers robust protection for primary amines under common synthetic conditions. Its bench-stable nature and compatibility with diverse reaction systems make it ideal for modular synthesis 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-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: