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Structure of 419572-19-3
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This tert-butyl exo-6-formyl-3-azabicyclo[3.1.0]hexane-3-carboxylate features a rigid, electron-deficient bicyclic scaffold with a strategically positioned formyl group at the exo-6 position. The tert-butyl ester enhances solubility and stability while enabling straightforward deprotection. This configuration supports efficient incorporation into complex molecular architectures requiring defined stereochemistry and reactive handles for downstream functionalization.
tert-Butyl exo-6-formyl-3-azabicyclo[3.1.0]hexane-3-carboxylate serves as a versatile, bench-stable building block for the synthesis of nitrogen-containing heterocycles and bioactive scaffolds. The exo-oriented formyl group enables direct functionalization via nucleophilic addition or oxime formation, while the protected carboxylic acid facilitates selective transformations. Its rigid bicyclic framework provides defined stereochemistry and excellent functional group tolerance, making it ideal for iterative synthesis in medicinal chemistry and process development workflows.
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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: