S 2 Oxo 1 2 5 7 Tetrahydrospiro Cyclopenta B Pyridine 6 3 Pyrrolo 2 3 B Pyridine 3 Carboxylicacid
pyridine pyrrole pyrazine piperidine piperazine

S)-2'-oxo-1',2',5,7-tetrahydrospiro[cyclopenta[b]pyridine-6,3'-pyrrolo[2,3-b]pyridine]-3-carboxylicacid

    Specifications

    HS Code

    686123

    Chemical Formula C17H13N3O3
    Molecular Weight 307.304 g/mol
    Appearance Solid (predicted)
    Solubility Poor solubility in water (predicted)
    Logp 1.61 (predicted)
    Stereochemistry S configuration at relevant chiral center
    Aromaticity Contains multiple aromatic rings
    Ring Count 4 rings

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    General Information
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    Frequently Asked Questions

    As a leading S)-2'-oxo-1',2',5,7-tetrahydrospiro[cyclopenta[b]pyridine-6,3'-pyrrolo[2,3-b]pyridine]-3-carboxylicacid supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the chemical structure of (S) -2 '-oxo-1', 2 ', 5,7-tetrahydrospiro [cyclopenta [b] pyridine-6,3' -pyrrolo [2,3-b] pyridine] -3-carboxylic acid?
    (* S *) - 2 '-oxo-1', 2 ', 5,7' -tetrahydrospiro [cyclopento [b] pyridine-6,3 '-pyrrolio [2,3-b] pyridine] -3 -carboxylic acid, this is an organic compound with a complex and delicate chemical structure.
    Looking at its structure, it has the appearance of a spiral ring. The two parts of cyclopento [b] pyridine and pyrrolio [2,3-b] pyridine are connected by a spiral atom, which is like a delicate chain of nature. On the side of the spiral atom, the cyclopento [b] pyridine ring contains a nitrogen atom, which imparts a certain alkalinity and reactivity to the ring. The pyrrolido [2,3-b] pyridine ring on the other side also has a unique electron cloud distribution, which affects each other, making the electronic effect of the whole spiral ring system complex.
    At the 2 'position, there is a carbonyl group (oxo group), which is a strong electron-absorbing group, which significantly affects the electron cloud density of surrounding atoms, and enhances the hydrogen acidity at the 2' position, which is easy to participate in the reaction. However, at a specific position in the spiral ring system, there are hydrogen atoms occupying, and its stereochemical environment is limited by the spiral ring, and the steric hindrance effect is obvious, which affects the molecular conformation and reaction selectivity. < Br >
    In the third position, there is a carboxyl group. The carboxyl group is both acidic and can undergo acid-base neutralization reactions. It can also participate in various organic reactions such as esterification, which greatly enriches the chemical properties of the compound and makes it potentially valuable in the fields of organic synthesis and medicinal chemistry. This compound has a unique structure, and its parts work together to build a delicate chemical structure. It is like a treasure carefully carved by ancient craftsmen, containing infinite chemical mysteries to be explored.
    (S) -2 '-oxo-1', 2 ', 5,7-tetrahydrospiro [cyclopenta [b] pyridine-6,3' -pyrrolo [2,3-b] pyridine] -3-carboxylic acid What are the physical properties?
    (S) -2 '-oxo-1', 2 ', 5,7' -tetrahydrospiro [cyclopento [b] pyridine-6,3 '-pyrrolio [2,3-b] pyridine] -3 -carboxylic acid, its physical properties are quite important, related to many properties of this compound.
    This substance is often a white to off-white solid powder with a fine and uniform state. This state is conducive to its uniform dispersion in many reaction systems, full contact with other reactants, and promotion of the reaction.
    Its melting point is of great significance for identification and purity determination. After experimental determination, the melting point is about a certain temperature range, which is its inherent property. If the melting point of the sample deviates from this range, it may suggest insufficient purity or change in crystal form.
    Solubility is also a key property. In common organic solvents, it exhibits a certain solubility in some polar organic solvents, such as ethanol and dimethyl sulfoxide. In ethanol, at a specific temperature, it can dissolve a certain amount. This solubility property is convenient for making it into a solution for chemical synthesis, drug development and many other fields. In non-polar organic solvents, such as n-hexane, the solubility is very small, which is related to the distribution of polar groups in the molecular structure. The force between the polar part and the non-polar solvent molecules is weak, resulting in difficulty in dissolution. < Br >
    In addition, its density also has a specific value. Although the value is not large, it is of great significance in some application scenarios that require density, such as in the preparation of preparations, which affects the final quality and performance of the product.
    The physical properties of this substance are interrelated and jointly affect its application in chemistry, medicine and other fields. It needs to be carefully considered in relevant research and production practice.
    (S) -2 '-oxo-1', 2 ', 5,7-tetrahydrospiro [cyclopenta [b] pyridine-6,3' -pyrrolo [2,3-b] pyridine] -3-carboxylic acid What are the common synthesis methods?
    (S) - 2 '-oxo-1', 2 ', 5,7-tetrahydrospiro [cyclopento [b] pyridine-6,3' -pyrrolio [2,3-b] pyridine] -3 -carboxylic acids are common synthetic methods, which are exquisite techniques in organic synthetic chemistry.
    First, it can be prepared by ingenious cyclization of compounds with similar structures. First, a suitable starting material is taken, and a series of carefully designed functional group transformations are carried out to gradually approach the molecular structure of the target product. If a specific pyridine and pyrrole derivative is used as a base, under suitable reaction conditions, various reagents are added with precise stoichiometry. Or use a strong acidic or alkaline medium to initiate an intra-molecular cyclization reaction. This process is similar to that of a craftsman carving jade. It is necessary to precisely control the temperature, time and proportion of the reactants in the reaction. If there is a slight difference, impurities may be formed or the expected product cannot be obtained.
    Second, the synthesis path catalyzed by transition metals is also quite commonly used. Transition metals such as palladium and rhodium are like magic wands that can activate specific chemical bonds. Complex with the metal with suitable ligands to arrange the reactants in an orderly manner around the metal center, thereby promoting the progress of the reaction. In this synthesis, the formation of carbon-carbon bonds or carbon-heteroatomic bonds catalyzed by metals can be used to form a spiral ring structure. Although this path is delicate, it requires a strict reaction environment. It needs to be operated under anhydrous and anaerobic conditions, and the cost of metal catalysts is high. Therefore, the advantages and disadvantages need to be weighed in practical applications.
    Third, biosynthesis has also emerged. With the help of enzymes in the body, highly selective synthesis can be achieved. Enzymes are like exquisite tools of nature, capable of catalyzing reactions under mild conditions. Screen specific microorganisms or extract specific enzymes, and use their specific identification of substrates to gradually synthesize simple biological small molecules into target products. This method is green and environmentally friendly, but the biological system is complex, and the preparation of enzymes and the optimization of reaction conditions are quite challenging. It needs to be carefully studied like exploring a mysterious maze.
    (S) -2 '-oxo-1', 2 ', 5,7-tetrahydrospiro [cyclopenta [b] pyridine-6,3' -pyrrolo [2,3-b] pyridine] -3-carboxylic acid in which applications?
    (* S *) -2 '-oxo-1', 2 ', 5,7' -tetrahydrospiro [cyclopento [b] pyridine-6,3 '-pyrrolio [2,3-b] pyridine] -3 -carboxylic acid, this compound has applications in pharmaceutical research and development, organic synthesis and other fields.
    In the field of pharmaceutical research and development, because of its unique chemical structure, it can be used as a lead compound. By modifying and optimizing its structure, drugs with novel structures and significant biological activities can be created. For example, a series of derivatives can be designed and synthesized for specific disease-related targets, such as abnormally expressed protein kinases in tumor cells, and through activity screening and pharmacological studies, anti-cancer drugs with high efficiency and low toxicity can be explored.
    In the field of organic synthesis, it can be used as a key intermediate to construct more complex heterocyclic compounds. Through organic synthesis methodologies, such as transition metal-catalyzed coupling reactions, cyclization reactions, etc., it can be combined with other functionalized reagents to realize the construction of complex spiro frameworks, providing new strategies and methods for the development of organic synthesis chemistry, enriching the molecular library of organic compounds, and laying the material foundation for new drug development, materials science and other fields.
    This compound is like a shining jade in the fields of medicine and organic synthesis. After being carved and polished, it will surely bloom more brilliantly and promote the progress and development of related fields.
    (S) -2 '-oxo-1', 2 ', 5,7-tetrahydrospiro [cyclopenta [b] pyridine-6,3' -pyrrolo [2,3-b] pyridine] -3-carboxylic acid What is the market outlook?
    (S) - 2 '-oxo-1', 2 ', 5,7-tetrahydrospiro [cyclopento [b] pyridine-6,3' -pyrrolio [2,3-b] pyridine] -3-carboxylic acid, which is a promising organic compound. In today's field of pharmaceutical research and development and organic synthesis, its market prospects are quite promising.
    In today's pharmaceutical industry, the creation of new drugs is a top priority. Many scientific research teams are doing their best to explore compounds with unique pharmacological activities, hoping to develop innovative drugs with excellent efficacy and mild side effects. ( S) - 2 '-oxo-1', 2 ', 5,7' -tetrahydrospiro [cyclopento [b] pyridine-6,3 '-pyrrolio [2,3-b] pyridine] -3 -carboxylic acid's unique molecular architecture makes it possible to interact with specific targets in vivo, and may become a key starting material for the development of new drugs.
    In the field of organic synthesis, chemists are keen to explore novel synthesis paths and methods to improve the synthesis efficiency and yield of such complex compounds. Efficient synthesis of this compound can not only reduce production costs, but also promote its industrial production process.
    However, the road ahead for this compound in the market is not smooth. Its large-scale production requires overcoming many technical difficulties, such as precise control of reaction conditions and effective removal of impurities. And the research and development of new drugs takes a long time and costs a lot. From compound screening to clinical application, there are many risks.
    Despite the difficulties and obstacles, (S) -2 '-oxo-1', 2 ', 5,7-tetrahydrospiro [cyclopento [b] pyridine-6,3' -pyrrolio [2,3-b] pyridine] -3-carboxylic acids still have considerable prospects in the pharmaceutical and organic synthesis markets due to their unique structure and potential activities. It is expected to add a strong touch to the development of human health and organic chemistry.