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*For research and further manufacturing use only, not for direct human use.
Structure of 3721-26-4
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This chiral cyclopropanamine features a rigid, strained three-membered ring system with defined stereochemistry at the 1R,2S configuration. The phenyl group imparts aromatic character and steric influence, while the primary amine enables facile derivatization. Ideal for asymmetric synthesis and medicinal chemistry applications requiring conformational constraint and precise spatial orientation.
(1R,2S)-2-Phenylcyclopropan-1-amine serves as a stereochemically defined building block for bioactive molecule synthesis, offering high functional group tolerance and bench stability. Its constrained cyclopropane scaffold enables precise spatial orientation in medicinal chemistry applications, facilitating efficient coupling reactions and serving as a key intermediate in the construction of heterocyclic frameworks relevant to CNS-targeted therapeutics.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: