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Structure of 1350713-44-8
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This chiral carbamate features a tert-butyl-protected (R)-3-oxobutan-2-yl group, enabling direct incorporation into asymmetric synthesis workflows. The ketone moiety provides a handle for stereoselective transformations, while the bench-stable tert-butyl carbamate offers reliable protection under standard conditions.
tert-Butyl (R)-(3-oxobutan-2-yl)carbamate serves as a chiral building block for asymmetric synthesis, enabling the efficient construction of β-keto amine motifs. Its stability under standard reaction conditions and compatibility with diverse transformations—such as reductive amination, enolate formation, and coupling reactions—facilitates streamlined access to complex intermediates in medicinal chemistry and natural product synthesis.
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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: