3ar 6s 7as 8 8 Dimethylhexahydro 3a 6 Methano 2 1 Benzothiazole 2 2 Dioxide
quinoline thiophene imidazole thiazole

(3aR,6S,7aS)-8,8-dimethylhexahydro-3a,6-methano-2,1-benzothiazole 2,2-dioxide

    Specifications

    HS Code

    693009

    Chemical Formula C12H19NO2S
    Molar Mass 241.35 g/mol

    As an accredited (3aR,6S,7aS)-8,8-dimethylhexahydro-3a,6-methano-2,1-benzothiazole 2,2-dioxide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing
    Storage
    Shipping
    Free Quote

    Competitive (3aR,6S,7aS)-8,8-dimethylhexahydro-3a,6-methano-2,1-benzothiazole 2,2-dioxide prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to info@alchemist-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: info@alchemist-chem.com

    General Information
    Where to Buy (3aR,6S,7aS)-8,8-dimethylhexahydro-3a,6-methano-2,1-benzothiazole 2,2-dioxide in China?
    As a trusted (3aR,6S,7aS)-8,8-dimethylhexahydro-3a,6-methano-2,1-benzothiazole 2,2-dioxide 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 (3aR,6S,7aS)-8,8-dimethylhexahydro-3a,6-methano-2,1-benzothiazole 2,2-dioxide 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 (3aR, 6S, 7aS) -8,8 -dimethylhexahydro-3a, 6 -methylene-2,1 -benzothiazole 2,2 -dioxide?
    The " (3aR, 6S, 7aS) -8,8-dimethyltetrahydro-3a, 6-methylene-2,1-benzofuran 2,2-dioxide" mentioned by you is an organic compound. Its structure is quite complex and needs to be analyzed in a fine way.
    The core structure of this compound is a benzofuran ring, which is formed by fusing the benzene ring and the furan ring, and has special stability and reactivity. At the 2,2 position, there is a dioxide group, which has a great influence on the electron cloud distribution and chemical properties of the compound, or gives it unique redox properties.
    Furthermore, at positions 3a and 6, methylene is connected to form a bridge-ring structure, which increases its steric hindrance and rigidity, and affects the conformation and reaction selectivity of molecules. The dimethyl substitution at positions 8 and 8 also contributes to the physical and chemical properties of molecules, or changes their polarity, solubility, and interactions with other molecules.
    The overall structure of this compound is like a delicate machine, and the cooperation of each part determines its unique chemical behavior. The delicate structure provides a wealth of research materials for the fields of organic synthesis and medicinal chemistry, or can be used to develop new drugs or functional materials.
    What are the physical properties of (3aR, 6S, 7aS) -8,8-dimethylhexahydro-3a, 6-methylene-2,1-benzothiazole 2,2-dioxide?
    (3aR, 6S, 7aS) - 8,8 - dimethyltetrahydro - 3a, 6 - methylene - 2,1 - benzofuran - 2,2 - dioxide, this substance has a variety of physical properties. Its properties are mostly crystalline, because its molecular structure contains specific atoms and groups arranged, causing intermolecular forces to form a regular lattice structure at room temperature and pressure, showing a crystalline state. In terms of melting point, due to the type and strength of intermolecular forces, a specific temperature range will change from solid to liquid. Generally speaking, the melting point of this type of benzofuran-containing structure and dioxy group compounds is relatively high. This is due to the conjugated system of the benzene ring in the structure and the polarity of the dioxy group, which enhances the intermolecular forces and requires more energy to overcome the lattice energy to melt.
    In terms of solubility, due to the presence of polar dioxy groups and relatively non-polar benzofuran skeletons, there is a certain solubility in polar organic solvents such as ethanol and acetone, and polar groups form hydrogen bonds or dipole-dipole interactions with solvent molecules; in non-polar solvents such as n-hexane, the solubility is low, because the non-polar part interacts weakly with the non-polar solvent.
    The density is affected by the molecular weight and the way of packing. The molecule contains multiple atoms with a certain mass, and the molecules are tightly packed in the crystal structure, so that the density is relatively large. The specific value is determined accurately, but the overall density range of compounds containing similar structures and atomic compositions is consistent.
    The physical properties of this substance are determined by its unique molecular structure, and these properties are of great significance in the fields of medicinal chemistry, materials science, etc. For example, drug development can use its solubility and stability characteristics to design dosage forms, and the material field can be used to prepare specific functional materials according to melting point and density characteristics.
    What are the main uses of (3aR, 6S, 7aS) -8,8-dimethylhexahydro-3a, 6-methylene-2,1-benzothiazole 2,2-dioxide?
    (3aR, 6S, 7aS) - 8,8 - dimethyltetrahydro - 3a, 6 - methylene - 2,1 - benzofuran - 2,2 - dioxides, this substance has a wide range of uses.
    In the field of medicine, it has unique pharmacological activities, or can be used in human physiological systems through specific mechanisms. For example, it may participate in cell signaling processes and have a regulatory effect on certain disease-related signaling pathways, thus laying the foundation for the creation of new drugs. Or for specific diseases such as inflammation, tumors, etc., it shows therapeutic potential, and is expected to become a new therapeutic drug through in-depth research and clinical trials.
    In the field of materials science, the structural properties of the substance may endow the material with special properties. If it is incorporated into polymer materials, it can change the mechanical properties of the material, such as enhancing the toughness and hardness of the material, improving the durability and stability of the material, and broadening the application scenarios of materials, such as application in aerospace, automobile manufacturing and other fields that require strict material properties.
    In the field of organic synthetic chemistry, it can be used as a key intermediate. With the help of organic synthesis methods, it can be used as a starting material and through a series of chemical reactions to derive organic compounds with diverse structures and functions, greatly enriching the variety of organic compounds, injecting vitality into the development of organic synthetic chemistry, and promoting the frontier research of organic synthetic chemistry to a new height.
    What are the synthesis methods of (3aR, 6S, 7aS) -8,8-dimethylhexahydro-3a, 6-methylene-2,1-benzothiazole 2,2-dioxide?
    To prepare (3aR, 6S, 7aS) -8,8-dimethyltetrahydro-3a, 6-methylene-2,1-benzocycloheptene-2,2-dioxide, there are many methods.
    First, a suitable starting material can be found to build a skeleton with delicate reaction steps. First, a certain aromatic hydrocarbon derivative is used as a base, and a specific group is introduced by a reaction such as electrophilic substitution to make it have the basis for constructing the target structure. Then, through cyclization, the structure of benzocycloheptene is initially formed. Under appropriate conditions, the oxidation reaction is used to precisely add the part of the dioxide, and attention is paid to the regulation of the reaction conditions at each step. Temperature, solvent, and catalyst are all critical, and detailed consideration is required to ensure that the reaction proceeds in the expected direction and high-purity products are obtained.
    Second, you can start from compounds with similar structures, and undergo functional group transformation and structural modification to achieve the purpose. First select compounds with similar carbon frames, adjust their structures through reactions such as elimination and addition, and gradually approach the contours of the target. Following oxidation, the required two oxide structures are obtained. In this process, it is particularly important to control the selectivity of the reaction, so as not to generate many by-products, which make it difficult to separate and purify the products.
    Third, we can also consider the use of modern organic synthesis techniques, such as transition metal catalysis reactions. By leveraging the unique activity of transition metal catalysts, the efficient construction of carbon-carbon bonds and carbon-hetero bonds can be achieved. Carefully select catalysts and ligands to regulate reaction activity and selectivity. In a suitable reaction system, each reactant can react in an orderly manner, and gradually piece together the complex structure of the target molecule. Although this approach is challenging, if successful, it may bring efficient and novel methods for synthesis.
    In short, the synthesis of this compound requires comprehensive consideration of the availability of starting materials, the difficulty of reaction, yield and purity, and many other factors. After repeated attempts and optimization, a satisfactory synthesis method can be obtained.
    (3aR, 6S, 7aS) -8,8-Dimethylhexahydro-3a, 6-methylene-2,1-benzothiazole 2,2-dioxide What are the precautions during use?
    (3aR, 6S, 7aS) -8,8-dimethyltetrahydro-3a, 6-methylene-2,1-benzocycloheptene 2,2-dioxide oxide should pay attention to the following matters during use:
    First, the properties of this substance are quite critical. Its structure is special and contains specific functional groups, which give it unique chemical activity and reaction characteristics. When using it, you must be familiar with its chemical properties in order to anticipate its possible reactions with other substances. In this way, it can effectively avoid the occurrence of unexpected reactions, thereby preventing the formation of dangerous products or causing deviations in the experimental and production processes.
    Second, safety should not be underestimated. Be sure to fully understand its possible effects on the human body, such as whether it is toxic, irritating or allergenic. During operation, it is necessary to strictly follow safety procedures and wear appropriate protective equipment, such as gloves, goggles and protective clothing, to protect yourself. Moreover, the use field needs to ensure good ventilation to prevent its volatile gases from accumulating in the air and causing potential health hazards.
    Third, storage conditions cannot be ignored. It is necessary to choose a suitable storage environment according to its physical and chemical properties. If it is not stored properly, it is very likely to cause it to deteriorate, which will affect the use effect. Generally speaking, it should be stored in a dry, cool and ventilated place, away from fire, heat and oxidants and other substances that may react with it.
    Fourth, accurate measurement is indispensable. Whether it is used for experimental research or industrial production, the dosage must be precisely controlled. Too much or too little dosage may have adverse effects on the reaction results or product quality. Therefore, it is necessary to use accurate measuring instruments and add them accurately according to the established formula or experimental requirements.
    Fifth, the record of the use process is also key. It is necessary to record the time of use, dosage, reaction conditions and observed phenomena in detail. These records are not only helpful for subsequent analysis and summary of the experiment or production process, but also can be used to quickly identify the cause and take appropriate solutions when problems occur.