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Structure of 1228561-56-5
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(αS)-3-Chloro-2-fluoro-α-methylbenzenemethanamine features a chiral α-methyl group and ortho-halogen substitution, delivering enhanced metabolic stability and defined stereochemical control. This bench-stable arylalkylamine integrates readily into CNS-targeted pharmacophores, enabling precise modulation of receptor interactions in medicinal chemistry campaigns.
(αS)-3-Chloro-2-fluoro-α-methylbenzenemethanamine serves as a chiral building block for the synthesis of bioactive compounds, enabling stereoselective incorporation of fluorinated aryl motifs. Its ortho-halogenated benzene core facilitates downstream coupling reactions, while the α-methyl group enhances metabolic stability and conformational rigidity. The compound exhibits bench stability and compatibility with standard synthetic workflows, supporting efficient purification and use in medicinal chemistry campaigns targeting CNS agents and kinase inhibitors.
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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 : P280-P301+P330+P331
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Lot numbers can be found on the outside label of a product: