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*For research and further manufacturing use only, not for direct human use.
Structure of 3513-81-3
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2-Methylene-1,3-propanediol features a reactive exocyclic methylene group flanked by two hydroxyl-bearing carbons, enabling efficient incorporation into polymer backbones and crosslinking networks. This bifunctional diol delivers enhanced reactivity under mild conditions while maintaining stability during storage.
2-Methylene-1,3-propanediol serves as a versatile synthon in organic synthesis, enabling efficient access to α,β-unsaturated carbonyl systems and heterocyclic scaffolds. Its bifunctional hydroxyl groups and reactive exocyclic methylene moiety facilitate regioselective transformations, including etherification, esterification, and cyclization reactions. The compound exhibits good bench stability and compatibility with standard purification methods, making it a practical building block for 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: