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Structure of 10300-69-3
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2-Chloroacetimidamide hydrochloride offers a stable, moisture-tolerant platform for imine-based transformations. This bench-stable reagent integrates readily into synthetic sequences requiring nitrogen transfer or electrophilic amidation. The chloride-bearing imidamide moiety enables efficient coupling with nucleophiles under mild conditions, streamlining access to functionalized heterocycles and amine derivatives in medicinal chemistry workflows.
2-Chloroacetimidamide hydrochloride serves as a versatile building block in synthetic organic chemistry, enabling the efficient construction of nitrogen-containing heterocycles and functionalized imidates. Its stability under standard bench conditions and compatibility with diverse reaction environments facilitate straightforward incorporation into complex molecular architectures. The compound functions as a key reagent in the synthesis of medicinally relevant scaffolds, particularly those requiring controlled amidine or guanidine formation.
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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-P405-P501
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Lot numbers can be found on the outside label of a product: