3as 12bs 5 Chloro 2 Methyl 2 3 3a 12b Tetrahydro 1h Dibenzo 2 3 6 7 Oxepino 4 5 C Pyrrole
pyridine pyrrole pyrazine piperidine piperazine

(3aS,12bS)-5-chloro-2-methyl-2,3,3a,12b-tetrahydro-1H-dibenzo[2,3:6,7]oxepino[4,5-c]pyrrole

    Specifications

    HS Code

    125465

    Chemical Name (3aS,12bS)-5-chloro-2-methyl-2,3,3a,12b-tetrahydro-1H-dibenzo[2,3:6,7]oxepino[4,5-c]pyrrole
    Molecular Formula C16H14ClNO
    Molecular Weight 271.74

    As an accredited (3aS,12bS)-5-chloro-2-methyl-2,3,3a,12b-tetrahydro-1H-dibenzo[2,3:6,7]oxepino[4,5-c]pyrrole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Competitive (3aS,12bS)-5-chloro-2-methyl-2,3,3a,12b-tetrahydro-1H-dibenzo[2,3:6,7]oxepino[4,5-c]pyrrole prices that fit your budget—flexible terms and customized quotes for every order.

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    General Information
    Where to Buy (3aS,12bS)-5-chloro-2-methyl-2,3,3a,12b-tetrahydro-1H-dibenzo[2,3:6,7]oxepino[4,5-c]pyrrole in China?
    As a trusted (3aS,12bS)-5-chloro-2-methyl-2,3,3a,12b-tetrahydro-1H-dibenzo[2,3:6,7]oxepino[4,5-c]pyrrole manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
    Frequently Asked Questions

    As a leading (3aS,12bS)-5-chloro-2-methyl-2,3,3a,12b-tetrahydro-1H-dibenzo[2,3:6,7]oxepino[4,5-c]pyrrole 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 -5-chloro-2-methyl-2, 3,3a, 12b-tetrahydro-1H-dibenzo [2,3:6,7] oxepino [4,5-c] pyrrole?
    The chemical structure of (3aS, 12bS) -5-chloro-2-methyl-2,3,3a, 12b-tetrahydro-1H-dibenzo [2,3:6,7] oxacycloheptano [4,5-c] pyrrole is a key content in the field of organic chemistry.
    The chemical structure of this compound can be carefully analyzed by its name. " (3aS, 12bS) " is the configuration of a specific chiral center, which follows the Cahn-Ingold-Prelog rule to accurately describe the stereochemical characteristics of the molecule. " 5-Chlorine ", indicating that the position of the chlorine atom in the molecular structure is at position 5;" 2-methyl ", the nail group is at position 2." 2,3,3a, 12b-tetrahydro "means that this molecule undergoes hydrogenation at positions 2, 3, 3a, and 12b, and some unsaturated bonds are saturated.
    " 1H-dibenzo [2,3:6,7] oxacycloheptano [4,5-c] pyrrole ", this core structure reveals that the molecule is formed by fusing dibenzo with oxacycloheptano and pyrrole ring. The dibenzo structure contains two benzene rings, which are fused in a specific way; the oxane heptano ring is an oxygen-containing seven-membered ring; the pyrrole ring is a nitrogen-containing five-membered heterocyclic ring. Each ring fuses with each other according to the positions marked in [2,3:6,7] and [4,5-c], forming a unique chemical skeleton.
    In summary, the chemical structure of (3aS, 12bS) -5-chloro-2-methyl-2,3,3a, 12b-tetrahydro-1H-dibenzo [2,3:6,7] oxacycloheptano [4,5-c] pyrrole is a complex organic molecular structure composed of specific chiral configurations, substituent positions and polycyclic fused, which is of great significance in many fields such as organic synthesis and pharmaceutical chemistry.
    (3aS, 12bS) What are the physical properties of -5-chloro-2-methyl-2, 3,3a, 12b-tetrahydro-1H-dibenzo [2,3:6,7] oxepino [4,5-c] pyrrole?
    (3aS, 12bS) -5 -chloro-2-methyl-2,3,3a, 12b-tetrahydro-1H-dibenzo [2,3:6,7] oxacycloheptano [4,5-c] pyrrole This substance has quite unique physical properties. Looking at its shape, under normal circumstances, it is mostly in a crystalline state, with a fine texture, like a natural crystal, radiant and regular.
    When it comes to color, it is often white to off-white, pure color, like the whiteness of first snow, and like the hazy and plain of morning fog, without the disturbance of variegated colors, showing the purity of quality.
    Smell its smell, almost tasteless, like a hermit hidden in the world, unobtrusive, without pungent smell to disturb people, tranquil and distant.
    Looking at its solubility, in organic solvents, such as ethanol, dichloromethane, etc., show certain solubility characteristics. Ethanol, like a warm and moist medium, can blend with the substance, partially dissolve, and form a uniform dispersion system; dichloromethane can also dissolve with it, showing good solubility. When the two dissolve, it is like water and milk, natural and harmonious.
    When talking about the melting point, the melting point of this substance is within a specific range, like its unique "identity". When the outside temperature gradually rises to near the melting point, the material is like ice in the warm sun, began to slowly melt, from solid to liquid gradually change, this process also witnessed its unique physical transformation, and the characteristics of the melting point, for the identification and purification of the material, is crucial, like the key to open the door to treasure, laying the foundation for further research and application.
    (3aS, 12bS) -5-chloro-2-methyl-2, 3,3a, 12b-tetrahydro-1H-dibenzo [2,3:6,7] oxepino [4,5-c] What is the purpose of pyrrole?
    (3aS, 12bS) - 5-chloro-2-methyl-2,3,3a, 12b-tetrahydro-1H-dibenzo [2,3:6,7] oxacycloheptano [4,5-c] pyrrole, this is a complex organic compound. Its uses are quite extensive, in the field of medicine, or have unique medicinal effects. Based on this delicate formula, doctors can develop a cure for intractable diseases, or have a significant effect on the treatment of specific diseases, bringing hope for recovery to patients.
    In the process of scientific research and exploration, this compound is also an important research object. Scientists use its unique chemical structure and properties to explore the mysteries of organic chemistry, delve into reaction mechanisms, expand the boundaries of chemical knowledge, and promote the progress and development of chemistry.
    In the field of materials science, or due to its own special properties, it can be used to prepare new materials. This material may have unique physical and chemical properties, showing extraordinary application potential in electronics, optics and other fields, injecting vitality into the innovation and development of materials science.
    In conclusion, (3aS, 12bS) - 5 - chloro - 2 - methyl - 2,3,3a, 12b - tetrahydro - 1H - dibenzo [2,3:6,7] oxacycloheptano [4,5 - c] pyrrole has important uses in many fields such as medicine, scientific research and materials science. It is like a bright pearl, bringing infinite possibilities for the development of various fields.
    (3aS, 12bS) What are the synthesis methods of -5-chloro-2-methyl-2, 3,3a, 12b-tetrahydro-1H-dibenzo [2,3:6,7] oxepino [4,5-c] pyrrole?
    The synthesis method of (3aS, 12bS) -5 -chloro-2-methyl-2,3,3a, 12b-tetrahydro-1H-dibenzo [2,3:6,7] oxacycloheptano [4,5-c] pyrrole is quite complicated and needs to be carried out according to fine steps.
    First, the method of selecting the starting material can be adopted. Select a suitable benzo derivative, whose structure needs to be in line with the reaction guidance, which can pave the way for subsequent cyclization and the introduction of functional groups. Here, the position and activity of the substituent of the raw material should be carefully observed to ensure the high efficiency and accuracy of the reaction.
    The nucleophilic substitution reaction is performed. In a suitable reaction medium, chlorine atoms are introduced with halogenated reagents. This step requires temperature control, time control, and selection of suitable bases to promote the effective action of nucleophiles and substrates to obtain chlorine-containing intermediates.
    Furthermore, the cyclization reaction is the key. With suitable catalysts and reaction conditions, the intramolecular ring formation is driven to construct a dibenzooxy heterocyclic heptyrrole skeleton. In this process, factors such as the type and dosage of catalysts and the polarity of the solvent have a significant impact on the cyclization efficiency and product configuration.
    In addition, the methylation step is also indispensable. The methylation reagent is used to introduce methyl at a specific activity check point. The reaction conditions need to be carefully adjusted to avoid side reactions and ensure the accuracy of methylation.
    At the end, the purification and characterization of the product are crucial. The product is purified by column chromatography, recrystallization and other methods, and then the structure and purity of the product are confirmed by spectroscopic analysis such as NMR and IR to conform to the expected (3aS, 12bS) configuration.
    Synthesis of this compound requires careful handling of each step and detailed control of the reaction parameters before the target product can be obtained.
    (3aS, 12bS) -5-chloro-2-methyl-2, 3,3a, 12b-tetrahydro-1H-dibenzo [2,3:6,7] oxepino [4,5-c] What is the market outlook for pyrrole?
    (3aS, 12bS) - 5-chloro-2-methyl-2,3,3a, 12b-tetrahydro-1H-dibenzo [2,3:6,7] oxacycloheptano [4,5-c] pyrrole, this substance is worthy of careful study in the current market prospects.
    Looking at today's pharmaceutical and chemical fields, this compound may have unique potential. Its structure is special, or it shows extraordinary efficacy in the development of new drugs. Due to the close relationship between structure and activity, the unique structure may be able to target specific biological targets, finding new ways in the treatment of diseases.
    In the course of scientific research and exploration, many scholars and scientific research groups have invested in compounds with similar structures. If this substance can emerge in the study of pharmacological activity, attract the attention of pharmaceutical companies, invest resources in research and development, and have the opportunity to enter the ranks of drug candidates in the future. In time, if the research and development goes well and the clinical trials are successful, it will be able to occupy a place in the pharmaceutical market and find a new chapter for the well-being of patients.
    Furthermore, in the field of fine chemicals, it may serve as a key intermediate to derive a series of high-value-added products. With the advancement of chemical technology, the development and utilization of its derivatives may become a trend. In this way, the market demand may increase due to the expansion of the industrial chain.
    However, its market prospects are not entirely smooth. The high cost of research and development and strict regulations and supervision are all obstacles to progress. Only by breaking through many difficulties can this material be expected to shine in the market, start its unique market journey, and paint a unique picture in the field of medicine and chemical industry.