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Structure of 109-54-6
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This chloroamine derivative features a reactive chloride at the β-position, enabling efficient alkylation under mild conditions. The dimethylamino group enhances nucleophilicity and solubility in polar solvents, facilitating use in synthetic transformations requiring stable, bench-ready amine equivalents.
3-Chloro-N,N-dimethylpropan-1-amine serves as a versatile bifunctional building block in synthetic organic chemistry, enabling efficient construction of nitrogen-containing heterocycles and medicinal intermediates. The chloro group facilitates nucleophilic substitution reactions, while the tertiary amine functions as a directing group or protonation site. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for modular synthesis workflows in API development and medicinal chemistry.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 2735
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314
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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: