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*For research and further manufacturing use only, not for direct human use.
Structure of 175021-13-3
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3-(Chloromethyl)cyclobutanone is a reactive cyclobutanone derivative featuring a chloromethyl group that enables efficient functionalization. This electrophilic handle facilitates nucleophilic substitution and conjugate addition reactions, serving as a key intermediate in the synthesis of complex cyclic architectures. The strained ring system enhances reactivity while maintaining stability under standard handling conditions.
3-(Chloromethyl)cyclobutanone serves as a versatile building block for the construction of functionalized cyclobutane scaffolds. The chloromethyl group enables nucleophilic substitution reactions, while the ketone functionality supports enolate chemistry and reductive transformations. Its bench-stable nature and compatibility with diverse reaction conditions facilitate efficient synthesis of complex heterocycles and medicinally relevant frameworks in organic and medicinal chemistry 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 : H225
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Precautionary Statements : P210-P243-P273-P403
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Lot numbers can be found on the outside label of a product: