Ethyl 1 Benzylhexahydropyrrolo 3 4 B Pyrrole 5 1h Carboxylate
pyridine pyrrole pyrazine piperidine piperazine

Ethyl 1-benzylhexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylate

    Specifications

    HS Code

    242101

    Chemical Formula C17H24N2O2
    Molecular Weight 288.385 g/mol
    Appearance Solid (Typical, but needs experimental verification)
    Solubility In Water Low (Expected due to non - polar groups)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform (Expected based on structure)
    Stability Stable under normal conditions, but sensitive to strong acids, bases and oxidizing agents (Expected based on functional groups)

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    Frequently Asked Questions

    As a leading Ethyl 1-benzylhexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylate 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 Ethyl 1-benzylhexahydropyrrolo [3,4-b] pyrrole-5 (1H) -carboxylate?
    Ethyl + 1 - benzylhexahydropyrrolo [3,4 - b] pyrrole - 5 (1H) -carboxylate, one of the organic compounds. Its chemical structure is quite complex, and it can be inferred from the naming convention.
    "Ethyl" means ethyl, which is a common substituent in organic chemistry, and has the structure of -C ² H. "1 - benzyl" indicates that there is a benzyl group in the first position of the molecular structure, and the structure of the benzyl group is -CH -2 - C H, which is formed by connecting the benzene ring to the methylene group.
    The "hexahydropyrrolo [3,4 - b] pyrrole" part, hexahydro - means hexahydro, indicating that there is a nitrogen-containing heterocyclic ring undergoing hexahydrogenation. Pyrrolo [3,4 - b] pyrrole shows that the heterocyclic ring is formed by fusing two pyrrole rings, and the fusing method follows the rules of [3,4 - b]. Specifically, the two pyrrole rings fuse with each other at a specific position to form a unique ring structure.
    "5 (1H) -carboxylate" means that at the 5th position of the fused ring structure, and in the 1H state, there is a carboxylic acid ester group connected, that is, the -COO-R structure, where R is ethyl, forming the structure of ethyl carboxylate -COOCH
    In summary, the chemical structure of Ethyl + 1 - benzylhexahydropyrrolo [3,4 - b] pyrrole - 5 (1H) -carboxylate is, with hexahydropyrrole [3,4 - b] pyrrole fused ring as the core, with benzyl at the 1st position and carboxylate at the 5th position. This structure integrates a variety of functional groups with a specific ring structure, and may have specific properties and uses in the fields of organic synthesis and medicinal chemistry.
    What are the main uses of Ethyl 1-benzylhexahydropyrrolo [3,4-b] pyrrole-5 (1H) -carboxylate
    Ethyl+1-benzylhexahydropyrrolo%5B3%2C4-b%5Dpyrrole-5%281H%29-carboxylate, the Chinese name or 1-benzylhexahydropyrrole [3,4-b] pyrrole-5 (1H) -ethyl formate. This substance is more commonly used in the field of medicinal chemistry.
    In pharmaceutical research and development, it can be used as a key intermediate. The compound has a specific chemical structure and activity, and can construct complex drug molecules through a series of chemical reactions. For example, in the creation of a new type of anti-tumor drug, it can participate in the construction of the core parent nucleus. By modifying the surrounding groups of the parent nucleus, it can change the ability of the drug to bind to the target and improve the efficacy and selectivity of the drug.
    In the field of organic synthesis, it is often used as an important building block. Due to its unique structure, it can be spliced with other organic molecules through various reactions such as nucleophilic substitution and redox to synthesize organic materials or natural product analogs with novel structures and specific functions. For example, when synthesizing organic materials with special optical and electrical properties, it can be used to introduce specific structural fragments and endow the materials with unique properties.
    In addition, in chemical research, it is an important object for studying the reaction mechanism and structure-activity relationship of nitrogen-containing heterocyclic compounds. Through the exploration of its reactions, scientists can gain insight into the reaction laws of nitrogen-containing heterocyclic rings under different conditions, providing a basis for the development and optimization of new reactions, and also helping to deeply understand the relationship between molecular structure and biological activity, guiding rational drug design and research and development of new functional materials.
    Ethyl 1-benzylhexahydropyrrolo [3,4-b] pyrrole-5 (1H) -carboxylate
    Ethyl 1-benzylhexahydropyrrolo [3,4-b] pyrrole-5 (1H) -carboxylate is an organic compound. The method of synthesizing this compound should follow the principles of organic synthesis and follow common reactions and steps.
    To synthesize this compound, you can first take the starting material with suitable functional groups. Start with a nitrogen-containing heterocyclic compound and a reagent containing ester groups and benzyl groups, and go through multiple steps to achieve the goal. The first step may be a nucleophilic substitution reaction, so that the active check point of the nitrogen-containing heterocyclic ring is connected to the benzyl-containing reagent to form a key carbon-nitrogen bond. In this step, a suitable base and solvent need to be selected to promote the smooth progress of the reaction. The strength of the base and the polarity of the solvent both affect the reaction rate and yield.
    After that, or through cyclization, the hexahydropyrrole [3,4-b] pyrrole ring structure of the target molecule is constructed. This cyclization reaction can be achieved by suitable catalysts and reaction conditions. The type and amount of catalysts, as well as the reaction temperature and time, need to be finely regulated.
    In addition, ester groups can be introduced, or through esterification reactions, suitable alcohols can be reacted with carboxylic acids or their derivatives to form ethyl 1-benzylhexahydropyrrolo [3,4-b] pyrrole-5 (1H) -carboxylate. This step also requires attention to the reaction conditions, such as the type and dosage of acid catalyst, reaction temperature and time, to prevent side reactions from occurring.
    After each step of the reaction, appropriate separation and purification methods, such as column chromatography, recrystallization, etc. are required to remove impurities to obtain a pure product for the next step of the reaction. And throughout the synthesis process, the reaction conditions should be carefully controlled, and the reaction process should be monitored in real time to achieve high yield and purity. Successful synthesis of ethyl 1-benzylhexahydropyrrolo [3,4-b] pyrrole-5 (1H) -carboxylate.
    What are the physical properties of Ethyl 1-benzylhexahydropyrrolo [3,4-b] pyrrole-5 (1H) -carboxylate
    Ethyl + 1 - benzylhexahydropyrrolo [3,4 - b] pyrrole - 5 (1H) -carboxylate is one of the organic compounds. Its physical properties are worth exploring.
    Looking at its appearance, it is often in a solid state, or a white to light yellow powder. This color and shape are its intuitive physical characteristics. Its melting point is also a key physical property. It usually changes from solid to liquid in a specific temperature range. However, the exact melting point is determined by factors such as the purity of the compound and the measurement conditions. It needs to be determined by precise experiments to be clear.
    When it comes to solubility, it often has a certain solubility in organic solvents, such as common ethanol, chloroform, and dichloromethane. This is because the molecular structure of the compound contains groups that interact with organic solvents, so that it can be dispersed and dissolved in such solvents. In water, its solubility is relatively low, and the hydrophobic part of its molecular structure accounts for a large proportion.
    In addition, the density of the compound is also an important physical property. Although the specific value also needs to be accurately measured experimentally, in general, its density is similar to that of common organic compounds. Determination of density is crucial for understanding its distribution and behavior in a specific system.
    And its refractive index reflects the refractive properties of light as it propagates in the compound. This property is closely related to the molecular structure and intermolecular interactions of the compound, and is also one of the elements that characterize its physical properties. The molecular structure and purity can be further analyzed by accurately measuring the refractive index. The physical properties of
    Ethyl + 1 - benzylhexahydropyrrolo [3,4 - b] pyrrole - 5 (1H) -carboxylate are diverse and interrelated, and are of crucial significance in the study of its chemical behavior, synthesis process and application field.
    Ethyl 1-benzylhexahydropyrrolo [3,4-b] pyrrole-5 (1H) -carboxylate
    Ethyl + 1 - benzylhexahydropyrrolo [3,4 - b] pyrrole - 5 (1H) -carboxylate, this is an organic compound, often referred to as ethyl pyrrole-pyrrole-carboxylate. Its market prospect is related to many fields, and it is a complex and diverse situation.
    Looking at the field of medicine, this product may have potential medicinal value. In today's medical research, new molecules are often found to treat difficult diseases. If this compound has been studied and proved to have pharmacological activities, such as anti-tumor, antiviral, neuroprotective effects, etc., it must attract the attention of pharmaceutical companies. The pharmaceutical industry has always pursued high-efficiency and low-toxicity new drugs. Once its medicinal potential is revealed, many pharmaceutical companies will invest in research and development to seek new drug creation, and the market potential can be said to be huge. However, the road of new drug research and development is long and difficult, and it requires multiple rounds of rigorous experiments, from cell experiments, animal experiments to human clinical trials. The cost and risk of failure are also high.
    Looking at materials science, organic compounds are often the cornerstone of building new materials. If this compound can endow materials with special properties, such as fluorescence properties, high stability, unique electrical properties, etc., it may emerge in the fields of optoelectronic materials and polymer materials. With the development of today's technology, the requirements for material properties are increasing, and the demand for materials with special properties is also increasing. If it can meet the needs of the industry, it must occupy a place in the material market for the manufacture of display screens, sensors and other products.
    However, its marketing activities also face challenges. If the synthesis process is complex and expensive, it will limit its large-scale production and application. Furthermore, the market competition is fierce, and there are many similar or similar functional compounds. How to stand out requires strong technical and market strategy support.
    In summary, Ethyl + 1 - benzylhexahydropyrrolo [3,4 - b] pyrrole - 5 (1H) -carboxylate market prospects are broad, but opportunities and challenges coexist. Only through in-depth research, optimization of processes, and precise market positioning can it be expected to succeed in the market.