The product name is 6-chloro-4-hydroxy-3-metho-xycarbonyl-2h-thieno[2,3-e]-1,2-thiazine- 1,1-dioxide, with the CAS number 70374-51-5. It is offered by factory supply at a low price. This compound belongs to the category of thieno - thiazine derivatives. Chemically, it contains a thieno[2,3 - e]-1,2 - thiazine core structure with a chloro, hydroxy, and methoxycarbonyl substituent. The molecular formula and molecular weight can be determined through advanced chemical analysis methods, which play a crucial role in understanding its physical and chemical properties. Physically, it may have certain solubility characteristics in different solvents, such as organic solvents like ethanol, methanol, and chloroform. The melting point, boiling point, and density are also important parameters that can affect its storage and handling conditions.
6-chloro-4-hydroxy-3-metho-xycarbonyl-2h-thieno[2,3-e]-1,2-thiazine- 1,1-dioxide has a wide range of potential applications. In the pharmaceutical field, it can serve as an important intermediate for the synthesis of various drugs. Its unique chemical structure may endow it with certain biological activities, such as anti - inflammatory, anti - microbial, or anti - tumor properties. Scientists can modify and optimize this compound to develop new drug candidates with higher efficacy and fewer side effects. In the chemical research area, it can be used as a building block in the synthesis of complex organic molecules. By reacting with different reagents, it can participate in various organic reactions, such as substitution reactions, addition reactions, and condensation reactions, to produce novel compounds with different structures and functions.
When using 6-chloro-4-hydroxy-3-metho-xycarbonyl-2h-thieno[2,3-e]-1,2-thiazine- 1,1-dioxide, proper safety precautions should be taken. Wear appropriate personal protective equipment, such as gloves and goggles, to avoid direct contact with the skin and eyes. In a laboratory or industrial setting, measure the required amount of the product accurately using proper measuring tools, such as pipettes or weighing scales. When dissolving the product, choose a suitable solvent based on its solubility characteristics. Stir or shake the solution gently to ensure complete dissolution. During the reaction process, control the reaction conditions carefully, including temperature, pressure, and reaction time, according to the specific reaction requirements. After the reaction, follow the standard procedures for product separation and purification, such as filtration, extraction, and distillation.
Case 1: Pharmaceutical Synthesis
A research team aimed to develop a new anti - inflammatory drug. They used 6-chloro-4-hydroxy-3-metho-xycarbonyl-2h-thieno[2,3-e]-1,2-thiazine- 1,1-dioxide as a key intermediate. First, they reacted it with a specific amine compound under controlled temperature and pH conditions. After a series of purification steps, they obtained a new compound. In vitro cell experiments showed that this new compound had significant anti - inflammatory activity, with a much lower cytotoxicity compared to existing drugs.
Case 2: Chemical Research
In a chemical laboratory, scientists were conducting research on the synthesis of new organic materials. They used 6-chloro-4-hydroxy-3-metho-xycarbonyl-2h-thieno[2,3-e]-1,2-thiazine- 1,1-dioxide to participate in a condensation reaction with an aldehyde compound. Through optimizing the reaction conditions, they successfully synthesized a novel conjugated organic molecule. This molecule exhibited excellent photoelectric properties, which had potential applications in the field of organic optoelectronics.
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