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The landscape of modern pharmaceutical research is built upon a foundation of precisely synthesized chemical compounds that serve as building blocks for novel drug candidates. Among these essential molecules is 3-(4-Nitro-1-oxo-1,3-dihydroisoindol-2-yl)piperidine-2,6-dione, readily identified by its CAS number 827026-45-9. This compound is not only recognized for its role as a pharmaceutical intermediate but also as a critical analog and potential impurity related to the widely used drug, Lenalidomide.
The synthesis of 3-(4-Nitro-1-oxo-1,3-dihydroisoindol-2-yl)piperidine-2,6-dione involves sophisticated organic chemistry techniques. As a nitro-containing heterocyclic compound, its structure presents specific reactive sites that chemists leverage for further molecular elaboration. The consistent production of this chemical intermediate, often to very high purity standards, is crucial for ensuring the reliability of subsequent research and manufacturing processes. Pharmaceutical intermediate synthesis is a specialized field, and access to well-characterized compounds like this is vital for researchers aiming to buy and utilize them effectively.
Its utility extends to being a valuable Lenalidomide analog. This characteristic makes it indispensable for researchers investigating the structure-activity relationships of immunomodulatory drugs, understanding drug metabolism, or developing analytical methods for quality control. The availability of such compounds as chemical research reagents empowers scientists to explore new therapeutic avenues and refine existing drug production protocols. The price of such specialized chemicals reflects the complexity of their synthesis and purification.
Moreover, its designation as a potential impurity means that precise reference standards are required for pharmaceutical quality assurance. Companies like NINGBO INNO PHARMCHEM CO.,LTD. are instrumental in supplying these critical materials, ensuring that drug manufacturers can meet regulatory requirements and deliver safe, effective medications to patients. The continuous demand for such building blocks highlights the ongoing innovation within the pharmaceutical sector and the indispensable role of high-quality chemical intermediates.
Manufacturing Facilities
Professional Export Experience
to Global Customers
1. 20 years of R&D, manufacturing and sales experience, serving customers in 60 countries and regions around the world;
2. Own R&D laboratory, pilot platform and large-scale production workshop, which can meet the audit requirements of global customers;
3. We can satisfy customers' perfect transition from small scale lab requirements (gram level) to commercialization requirements (hundred tons level).
A: We don't have Minimum Order Quantity, exact quantity should be provided before quotation for us to calculate the exact cost.
A: We don't provide free samples due to lots of request and expensive international courier's cost, we can deduct the sample charge after commercial order placed.
A: Our payment terms: Small or sample order: T/T IN ADVANCE. Commercial order: First order should be by T/T IN ADVANCE or L/C at sight, and following orders T/T 30~90days is acceptable subject to approval of credit application.
