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Structure of 196404-55-4
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This oxazolidine derivative features a chiral scaffold with orthogonal functional handles: a tert-butoxycarbonyl group for selective protection and a para-methoxyphenyl moiety enhancing solubility. The carboxylic acid enables direct conjugation or derivatization, while the phenyl substituent imparts rigidity and steric control. Designed for use in asymmetric synthesis and peptide mimetic construction under standard bench conditions.
This chiral oxazolidine serves as a robust building block for the synthesis of bioactive heterocycles and peptidomimetics. Its well-defined stereochemistry enables predictable transformations, while the Boc-protected carboxylic acid and pendant aryl groups offer orthogonal functionality for sequential coupling reactions. Bench-stable and readily purified by chromatography, it facilitates efficient access to complex scaffolds in medicinal chemistry campaigns.
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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: