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Structure of 67341-01-9
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tert-Butyl (2-hydroxy-1-phenylethyl)carbamate delivers a protected hydroxyl group flanked by a chiral benzylic center, enabling stereocontrolled synthesis in complex molecule assembly. The carbamate moiety ensures stable protection under standard conditions while permitting selective deprotection via mild acidolysis. This scaffold integrates seamlessly into peptide and natural product frameworks, offering enhanced solubility and handling advantages in synthetic workflows.
tert-Butyl (2-hydroxy-1-phenylethyl)carbamate serves as a stable, bench-friendly chiral auxiliary for asymmetric synthesis, enabling stereoselective transformations via its protected hydroxyl and amine functionalities. The carbamate group facilitates efficient deprotection under mild acidic conditions, while the pendant phenyl and hydroxyl moieties support orthogonal functionalization in complex molecule assembly. Its robust stability and predictable reactivity make it a reliable building block for pharmaceutical intermediates and natural product synthesis.
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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: