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Structure of 223644-10-8
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(R)-tert-Butyl 3-methyl-1,4-diazepane-1-carboxylate features a chiral diazepane core with a bench-stable tert-butyl ester and a methyl group at the 3-position, enabling direct incorporation into complex heterocyclic scaffolds. This configuration supports stereocontrolled synthesis of bioactive nitrogen-rich compounds.
(R)-tert-Butyl 3-methyl-1,4-diazepane-1-carboxylate serves as a valuable chiral building block in medicinal chemistry, enabling the synthesis of saturated heterocyclic scaffolds with defined stereochemistry. The protected diamine functionality offers excellent stability and compatibility with standard coupling and reduction protocols. Its methyl substitution enhances metabolic stability and modulates physicochemical properties, making it particularly useful for constructing bioactive molecules in drug discovery programs.
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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-H312-H315-H319-H332-H335
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P304+P341-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P363-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: