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Structure of 1440-61-5
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4-(2-Chloroacetyl)morpholine features a morpholine ring bearing a chloroacetyl substituent, delivering a reactive acylating handle for conjugation chemistry. This bench-stable derivative enables efficient incorporation into peptide and small-molecule scaffolds under mild conditions, leveraging the electrophilic carbonyl for nucleophilic attack.
4-(2-Chloroacetyl)morpholine serves as a versatile building block in medicinal chemistry, enabling efficient access to morpholine-containing scaffolds via nucleophilic substitution or condensation reactions. The chloroacetyl group exhibits high reactivity toward amines and hydrazides, facilitating the construction of diverse heterocyclic systems. Its bench-stable nature and compatibility with standard purification methods make it well-suited for multi-step synthesis and scale-up applications.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H318-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: