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Structure of 74965-38-1
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tert-Butyl (2-formylphenyl)carbamate features a formyl group ortho to a carbamate moiety, enabling direct functionalization in late-stage synthesis. This bench-stable reagent integrates readily into diversification workflows, offering selective reactivity under mild conditions while maintaining compatibility with common protecting groups.
tert-Butyl (2-formylphenyl)carbamate serves as a versatile building block in medicinal chemistry, enabling efficient access to ortho-substituted benzaldehyde derivatives. The carbamate group provides stability and facilitates selective deprotection under mild acidic conditions, while the formyl functionality supports standard transformations including reductive amination, Wittig reactions, and nucleophilic additions. Its bench-stable nature and compatibility with diverse synthetic workflows make it ideal for constructing complex heterocyclic scaffolds and API intermediates.
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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: