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(S)- (+)-Oxiran-2-ylmethyl- 3-nitrobenzenesulfonate CAS:115314-14-2

(S)-(+)-Oxiran-2-ylmethyl-3-nitrobenzenesulfonate is a chiral epoxide compound featuring an oxirane ring and a nitrobenzenesulfonate group. This compound has garnered interest in organic synthesis due to its unique reactivity, primarily attributed to the strained three-membered epoxide ring, which is highly susceptible to nucleophilic attack. The specific stereochemistry of the (S)-(+) enantiomer provides distinct advantages in asymmetric synthesis, enabling the production of enantiomerically pure compounds. Research continues to explore its applications in medicinal chemistry and materials science, highlighting its potential as a versatile intermediate for synthesizing pharmaceuticals and fine chemicals.


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Application and Effect:

(S)-(+)-Oxiran-2-ylmethyl-3-nitrobenzenesulfonate, with the molecular formula C11H11N O5S, is characterized by its unique structure that consists of an epoxide (oxirane) moiety attached to a methyl group linked to a 3-nitrobenzenesulfonate. The presence of the oxirane ring makes this compound particularly valuable due to the inherent strain within the three-membered ring, which significantly enhances its reactivity and versatility in chemical transformations. The epoxide functionality allows for various nucleophilic substitution reactions, making (S)-(+)-oxiran-2-ylmethyl-3-nitrobenzenesulfonate a key intermediate in the synthesis of more complex organic molecules. Its chiral nature means that the (S)-(+) enantiomer can be used to generate products with specific stereochemical configurations, essential in the pharmaceutical industry where the biological activity of compounds often depends on their chiral purity. In medicinal chemistry, this compound’s ability to undergo selective ring-opening reactions opens up pathways to synthesize diverse therapeutic agents, including anti-cancer and anti-inflammatory drugs. The incorporation of the 3-nitrobenzenesulfonate group further enhances the electrophilic character of the molecule, facilitating the introduction of nucleophiles that can lead to functionalized derivatives with improved pharmacological properties. Additionally, (S)-(+)-oxiran-2-ylmethyl-3-nitrobenzenesulfonate has potential applications in the development of advanced materials. The epoxide can act as a cross-linking agent in polymer chemistry, contributing to the creation of thermosetting resins with desirable mechanical and thermal properties. Current research focuses on optimizing the synthetic routes to this compound, exploring new reaction conditions, and investigating its utility in various applications. By expanding the understanding of its reactivity and interactions, chemists can unlock further potential uses of (S)-(+)-oxiran-2-ylmethyl-3-nitrobenzenesulfonate in both academic and industrial settings. In conclusion, (S)-(+)-oxiran-2-ylmethyl-3-nitrobenzenesulfonate represents a significant compound in organic synthesis, with implications in drug development and material science, underscoring the importance of chiral intermediates in modern chemistry.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C9H9NO6S
Assay 99%
Appearance white powder
CAS No.  115314-14-2
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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