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(1R,2S)-2-(3,4-Difluorophenyl)cyclopropanamine (R)-2-hydroxy-2-phenylacetate CAS: 376608-71-8

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Catalog Number: XD93936
Cas: 376608-71-8
Molecular Formula: C17H17F2NO3
Molecular Weight: 321.32
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Product Detail

Product Tags

Catalog Number XD93936
Product Name (1R,2S)-2-(3,4-Difluorophenyl)cyclopropanamine (R)-2-hydroxy-2-phenylacetate
CAS 376608-71-8
Molecular Formula C17H17F2NO3
Molecular Weight 321.32
Storage Details Ambient

 

Product Specification

Appearance White powder
Assay 99% min

 

(1R,2S)-2-(3,4-Difluorophenyl)cyclopropanamine (R)-2-hydroxy-2-phenylacetate is a compound with a complex chemical structure consisting of a cyclopropane ring, a difluorophenyl group, and an acetate moiety, among others. This compound has various potential applications in the fields of pharmaceuticals and chemical synthesis due to its unique properties.One potential use of (1R,2S)-2-(3,4-Difluorophenyl)cyclopropanamine (R)-2-hydroxy-2-phenylacetate is as a pharmaceutical intermediate. Due to its structural features, this compound can serve as a building block for the synthesis of novel drug candidates. The cyclopropane ring offers rigidity and three-dimensional shape, which can be beneficial for drug-target interactions. The presence of the difluorophenyl group can introduce unique electronic and lipophilic properties, potentially improving the pharmacokinetics and efficacy of the final compound. Additionally, the acetate moiety can act as a protecting group, enabling the introduction and selective modification of other functional groups during the synthesis process.The (1R,2S)-stereoisomer in the structure further adds to the compound's versatility. Stereochemistry plays a crucial role in drug interactions, as different enantiomers can exhibit different pharmacological activities and metabolic profiles. The (1R,2S)-configuration of the cyclopropane ring and the acetate moiety can lead to the creation of enantiomerically pure compounds, which can then be used for targeted drug development and optimization.Furthermore, the difluorophenyl group in (1R,2S)-2-(3,4-Difluorophenyl)cyclopropanamine (R)-2-hydroxy-2-phenylacetate can contribute to the compound's potential applications in the field of chemical synthesis. The presence of fluorine atoms in organic molecules often enhances their stability, lipophilicity, and reactivity. This can make the compound suitable for reactions that require fluorinated building blocks or for the creation of fluorinated derivatives of existing compounds.It is important to note that the specific applications of (1R,2S)-2-(3,4-Difluorophenyl)cyclopropanamine (R)-2-hydroxy-2-phenylacetate will depend on the desired properties and requirements of the final product. Further research and development are necessary to explore the full potential of this compound in various fields, including pharmaceuticals and chemical synthesis.As with any chemical compound, proper handling, storage, and safety protocols should be followed when working with (1R,2S)-2-(3,4-Difluorophenyl)cyclopropanamine (R)-2-hydroxy-2-phenylacetate to ensure personal safety and prevent any environmental hazards.In conclusion, (1R,2S)-2-(3,4-Difluorophenyl)cyclopropanamine (R)-2-hydroxy-2-phenylacetate offers potential applications as a pharmaceutical intermediate and versatile building block in chemical synthesis. Its structural features, including the cyclopropane ring, difluorophenyl group, and acetate moiety, provide opportunities for the synthesis of diverse compounds with targeted pharmacological activities and improved properties. Further research is needed to fully explore its potential in various applications.


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    (1R,2S)-2-(3,4-Difluorophenyl)cyclopropanamine (R)-2-hydroxy-2-phenylacetate CAS: 376608-71-8