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Structure of 865450-09-5
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tert-Butyl(2-fluoro-4-formylphenyl)carbamate features a fluorinated aromatic core with a formyl group at the para position, enabling direct functionalization in late-stage synthesis. The carbamate handle provides stable protection for amine intermediates and facilitates purification. This bench-stable reagent integrates seamlessly into multi-step routes requiring selective aldehyde coupling or derivatization.
tert-Butyl(2-fluoro-4-formylphenyl)carbamate serves as a versatile building block for medicinal chemistry and process development, enabling direct functionalization at the formyl group via nucleophilic addition or condensation reactions. The ortho-fluoro substituent enhances electrophilicity at the adjacent carbonyl site and facilitates downstream coupling transformations. Its tert-butyl carbamate (Boc) protection ensures stability during purification and handling, while the formyl group offers high reactivity in standard amine-based cyclizations, oxime formations, and transition metal-catalyzed cross-couplings.
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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: