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*For research and further manufacturing use only, not for direct human use.
Structure of 101689-05-8
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(R)-Pentan-2-amine hydrochloride offers a chiral, bench-stable amine handle for asymmetric synthesis. This configurationally stable derivative integrates readily into catalytic systems and peptide backbones, providing high enantioselectivity in reductive amination and transition-metal-catalyzed transformations.
(R)-Pentan-2-amine hydrochloride serves as a chiral building block for asymmetric synthesis, enabling the construction of bioactive amines and pharmaceutical intermediates. Its bench-stable salt form facilitates handling and purification, while the stereogenic center supports enantioselective transformations. Functions effectively in amine coupling, reductive amination, and heterocycle formation under standard reaction conditions.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: