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Structure of 663172-78-9
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This tert-butyl ester derivative features a rigid bicyclic scaffold with a strategically positioned hydroxy group and a nitrogen heteroatom, enabling selective functionalization. The ester moiety enhances solubility and stability under standard conditions, facilitating downstream transformations in synthetic routes to complex alkaloids and bioactive heterocycles.
6-Hydroxy-3-aza-bicyclo[3.2.0]heptane-3-carboxylic acid tert-butyl ester serves as a versatile bicyclic scaffold for medicinal chemistry campaigns, enabling efficient access to constrained nitrogen-containing heterocycles. The tertiary alcohol and ester functionalities offer orthogonal handles for selective derivatization, while the tert-butyl ester ensures stability during storage and compatibility with standard deprotection protocols. Its rigid framework facilitates conformational control in target molecules, enhancing binding affinity and metabolic stability in drug discovery applications.
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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: