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Structure of 1269470-38-3
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(S)-3-Methyl-1-phenylbutan-1-amine hydrochloride is a chiral amine scaffold featuring a stereogenic center at the 3-position, enabling precise control in asymmetric synthesis. The phenyl group imparts rigidity and π-conjugation, while the protonated amine enhances solubility and facilitates salt formation for improved handling. This bench-stable derivative serves as a key building block in medicinal chemistry, particularly for designing enantioselective catalysts and bioactive molecules requiring defined stereochemistry.
(S)-3-Methyl-1-phenylbutan-1-amine hydrochloride serves as a chiral building block for asymmetric synthesis, enabling the construction of biologically relevant amine scaffolds. Its bench-stable hydrochloride salt form facilitates handling and purification, while the stereogenic center supports enantioselective transformations. The molecule functions effectively in reductive amination, coupling reactions, and as a ligand precursor in transition metal catalysis.
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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: