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Structure of 1253790-80-5
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This bench-stable chiral amine features a (R)-configured stereocenter adjacent to a 4-chloro-3-fluorophenyl group, delivering high enantiomeric purity. The hydrochloride salt enhances solubility and handling stability, enabling efficient integration into asymmetric synthesis workflows for pharmaceutical intermediates.
(R)-1-(4-Chloro-3-fluorophenyl)ethan-1-amine hydrochloride serves as a chiral building block for the synthesis of bioactive molecules, particularly in medicinal chemistry and API development. Its well-defined stereochemistry enables consistent enantioselective transformations. The compound exhibits good bench stability, ease of handling, and compatibility with standard amine functional group manipulations, including acylation, alkylation, and coupling reactions. It functions as a key intermediate in constructing arylalkylamine motifs found in pharmaceutical scaffolds.
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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 : H302-H315-H319-H335
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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: