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Structure of 335255-43-1
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tert-Butyl (2-amino-4-(thiophen-2-yl)phenyl)carbamate features a thiophene-substituted aniline scaffold with a protected amine, enabling direct incorporation into complex heterocyclic architectures. The boronate moiety offers robust stability under standard conditions, facilitating efficient cross-coupling transformations in medicinal chemistry and materials synthesis.
tert-Butyl (2-amino-4-(thiophen-2-yl)phenyl)carbamate serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted aniline derivatives via mild deprotection. The thiophene moiety provides π-conjugation and orthogonal reactivity, while the tert-butyl carbamate group offers excellent bench stability and facile removal under acidic conditions. Its compatibility with standard coupling reactions and functional group tolerance makes it ideal for constructing bioactive heterocyclic scaffolds and peptide-like intermediates in drug discovery 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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: