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Structure of 127310-66-1
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cis-(1-Benzylazetidine-2,4-diyl)dimethanol features a rigid, cis-configured azetidine core with two pendant hydroxymethyl groups, enabling precise spatial control in molecular scaffolding. The benzyl substituent enhances solubility and provides a handle for further derivatization, while the diol functionality supports hydrogen bonding and integration into complex synthetic intermediates.
cis-(1-Benzylazetidine-2,4-diyl)dimethanol serves as a versatile chiral building block for the synthesis of nitrogen-containing heterocycles and bioactive scaffolds. Its cis-configured azetidine core exhibits enhanced stability and predictable stereochemistry, enabling efficient functionalization at both C2 and C4 positions. The pendant benzyl group provides orthogonal reactivity, while the two primary alcohol functionalities facilitate conjugation, derivatization, or protection strategies in multi-step syntheses. This compound functions reliably in standard coupling, cyclization, and modification protocols common to 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: