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Structure of 320590-29-2
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Benzyl (3-oxocyclohexyl)carbamate features a carbamate-protected amine tethered to a cyclohexanone-derived scaffold, enabling selective functionalization in synthetic sequences. The pendant ketone facilitates downstream transformations such as reductive amination or nucleophilic addition. This compound offers enhanced stability under standard bench conditions and compatibility with diverse reaction environments.
Benzyl (3-oxocyclohexyl)carbamate serves as a versatile protecting group for primary amines, combining the stability of the benzyl moiety with the synthetic flexibility of the 3-oxocyclohexyl scaffold. It facilitates efficient amine protection and subsequent deprotection under mild hydrogenolysis conditions, enabling clean functional group manipulation. The ketone functionality allows for further derivatization via enolate chemistry or reductive amination, making it valuable in multi-step synthesis of complex molecules. Its bench-stable nature and compatibility with diverse reaction conditions support robust application 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: