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Structure of 745011-75-0
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Boc-D-Homoserine features a protected D-homoserine backbone, enabling stable incorporation into peptide sequences and synthetic intermediates. The tert-butoxycarbonyl group ensures orthogonal handling during multi-step syntheses, while the chiral center supports stereoselective transformations in bioactive molecule construction.
Boc-D-Homoserine serves as a key chiral building block in peptide synthesis and medicinal chemistry, offering stable protection of the amine group under acidic conditions. Its hydroxyl functionality enables selective derivatization for heterocycle formation or conjugation strategies. The Boc group facilitates straightforward deprotection with trifluoroacetic acid, enabling efficient access to D-homoserine derivatives. This compound exhibits excellent bench stability and compatibility with standard coupling protocols, making it a practical choice for scalable synthesis and fragment assembly.
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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: