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Structure of 59408-74-1
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O-Benzyl-N-(tert-butoxycarbonyl)-L-homoserine features a protected hydroxyl group and a stable tert-butyl carbamate handle, enabling reliable incorporation into peptide sequences. This derivative delivers enhanced solubility and stability during solid-phase synthesis workflows, facilitating efficient chain elongation in complex peptide assembly.
O-Benzyl-N-(tert-butoxycarbonyl)-L-homoserine serves as a versatile chiral building block in peptide and heterocycle synthesis, offering orthogonal protection for both hydroxyl and amine functionalities. The benzyl ether provides stable O-protection compatible with standard deprotection conditions, while the Boc group enables mild acid-labile N-protection. This combination facilitates sequential functionalization and purification under routine bench conditions, supporting efficient access to complex scaffolds 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-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: