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Structure of 2627-86-3
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(S)-(-)--Methylbenzylamine along with 2-formylphenylboronic acid has been used in a derivatization protocol to analyze the enantiomeric excess of chiral diols.It can also be used:In the diastereoselective synthesis of S-aminonitriles.As a chiral auxiliary in the synthesis of (S)-(-)-N-acetylcalycotomine or (R)-(+)-N-acetylcalycotomine.As a chiral building block in the asymmetric synthesis of 1-substituted tetrahydro--carbolines.
(S)-(-)-1-Phenylethanamine serves as a chiral building block for asymmetric synthesis, enabling stereoselective transformations in medicinal chemistry and catalyst development. Its bench-stable, enantiomerically pure form facilitates efficient resolution and functional group manipulation. Widely employed in the construction of bioactive molecules, it functions as a versatile scaffold for pharmaceutical intermediates and ligand design.
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GHS Pictogram :
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GHS No : GHS05,GHS06
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Signal Word : Danger
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UN#: 2922
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Class : 8 (6.1)
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Packing Group : Ⅱ
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Hazard Statements : H227-H302-H311-H314-H412
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Precautionary Statements : P210-P264-P270-P273-P280-P301+P330+P331-P304+P340-P361-P363-P370+P378-P405-P501
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Lot numbers can be found on the outside label of a product: