Product Description
Cigna Qingdao is mainly engaged in the intermediates of febuxostatin, ceflothrin, eprazole, flubiprofen, phenalidone, tovaptan, rivaroxaban and Avanafil, terbinafine intermediates, thioacetamide and thiophene and their derivatives.
AI Product Description
*The following content is generated by AI and is for reference only.
The compound designated as 2-{[(2S)-oxiran-2-yl]methyl}-2,3-dihydro-1H-isoindole-1,3-dione is a specialized chiral intermediate widely utilized in the pharmaceutical and agrochemical industries. Its chemical structure features a phthalimide core linked to an optically active epoxide ring via a methylene bridge. The (2S) configuration at the oxirane position is critical, as it ensures specific stereochemical outcomes in subsequent synthetic transformations, making this molecule a valuable building block for creating enantiomerically pure drugs.
The molecular formula of this substance is C₁₂H₁₁NO₄, with a molecular weight of approximately 233.22 g/mol. While specific catalog numbers vary by supplier, its identity is uniquely defined by its structural arrangement rather than a single universal CAS number, as it is often synthesized in-house or sourced as a custom intermediate. The presence of the highly reactive epoxide moiety allows for nucleophilic ring-opening reactions, which are fundamental steps in constructing complex nitrogen-containing heterocycles. Consequently, this compound serves as a pivotal precursor in the synthesis of beta-adrenergic blockers, antihypertensive agents, and various other bioactive amines.
In practical applications, researchers employ this material to introduce chiral centers into drug candidates with high precision. The phthalimide group acts as a robust protecting group for primary amines, preventing unwanted side reactions during multi-step syntheses while allowing for easy removal under mild conditions later in the process. This dual functionality—providing both chirality and protection—streamlines the manufacturing workflow for complex therapeutic molecules. Furthermore, the stability of the isoindole dione scaffold ensures reliable storage and handling compared to more labile alternatives.
Due to its niche status as a fine chemical intermediate, it is primarily available through specialized chemical distributors catering to research laboratories and contract manufacturing organizations. Strict adherence to safety protocols is recommended when handling the epoxide component, given its potential reactivity with biological tissues. As the demand for stereoselective synthesis grows in modern medicinal chemistry, compounds like 2-{[(2S)-oxiran-2-yl]methyl}-2,3-dihydro-1H-isoindole-1,3-dione remain essential tools for developing next-generation therapeutics with improved efficacy and safety profiles.