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Structure of 176980-36-2
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tert-Butyl (3-formylphenyl)carbamate features a bench-stable carbamate-protected aldehyde group positioned meta to the aromatic ring. This functionalized scaffold enables direct incorporation into diverse synthetic sequences, including reductive amination and Wittig reactions, without requiring deprotection prior to coupling. The tert-butyl moiety ensures excellent stability under standard conditions.
tert-Butyl (3-formylphenyl)carbamate serves as a versatile building block in medicinal and synthetic chemistry, enabling direct introduction of a meta-substituted benzaldehyde moiety. The formyl group facilitates efficient transformations including reductive amination, Wittig reactions, and nucleophilic additions, while the carbamate protects the amine under standard reaction conditions. Bench-stable and easily purified, it functions as a key intermediate in the synthesis of heterocyclic scaffolds and bioactive molecules.
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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: