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Structure of 216002-20-9
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(R)-1-(3,5-Bis(trifluoromethyl)phenyl)ethanamine hydrochloride delivers a chiral amine scaffold with enhanced stability and solubility. The electron-deficient aromatic ring improves binding affinity in asymmetric synthesis, while the hydrochloride salt ensures ease of handling and crystallinity. This bench-stable compound integrates readily into catalyst design and medicinal chemistry workflows.
(R)-1-(3,5-Bis(trifluoromethyl)phenyl)ethanamine hydrochloride serves as a stable, bench-ready chiral building block for the synthesis of bioactive molecules. Its trifluoromethylated aromatic core enhances metabolic stability and lipophilicity, while the chiral amine functionality enables stereoselective transformations. The hydrochloride salt ensures excellent solubility and ease of handling, facilitating its use in standard coupling reactions, asymmetric synthesis, and API intermediate development.
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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: