S 4 5 Dihydro 2 6 Hydroxybenzothiazol 2 Yl Thiazole 4 Carboxylic Acid
quinoline thiophene imidazole thiazole

(S)-4,5-dihydro-2-(6-hydroxybenzothiazol-2-yl)thiazole-4-carboxylic acid

    Specifications

    HS Code

    983800

    Chemical Formula C11H8N2O3S2
    Molecular Weight 280.33 g/mol
    Appearance Solid (predicted)
    Melting Point No data available
    Boiling Point No data available
    Solubility No data available
    Density No data available
    Pka No data available
    Logp No data available
    Stereochemistry S - configuration at the relevant chiral center

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    General Information
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    Frequently Asked Questions

    As a leading (S)-4,5-dihydro-2-(6-hydroxybenzothiazol-2-yl)thiazole-4-carboxylic acid 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) -4,5-dihydro-2- (6-hydroxybenzothiazol-2-yl) thiazole-4-carboxylic acid?
    The chemical structure of (S) -4,5-dihydro-2- (6-hydroxybenzothiazole-2-yl) thiazole-4-carboxylic acid is an important research object in the field of organic chemistry. This compound has a unique chemical composition and spatial arrangement.
    Its core structure contains thiazole ring and benzothiazole ring. The thiazole ring is a five-membered heterocyclic ring composed of a sulfur atom, a nitrogen atom and three carbon atoms. In (S) -4,5-dihydro-2- (6-hydroxybenzothiazole-2-yl) thiazole-4-carboxylic acid, the 4-position of the thiazole ring is connected with a carboxyl group. This carboxyl group endows the compound with certain acidity and chemical reaction activity, and can participate in many acid-base reactions and esterification reactions.
    Furthermore, the 2-position of the thiazole ring is connected to the benzothiazole ring. The benzothiazole ring is formed by fusing a benzene ring with a thiazole ring. The degree of conjugation of the molecule is added to the fused ring structure, which affects its physical and chemical properties. And the 6-position of the benzothiazole ring is connected with a hydroxyl group. The presence of the hydroxyl group can enhance the hydrophilicity of the molecule and participate in the formation of hydrogen bonds, which has an important impact on the intermolecular interaction and crystal structure.
    The 4,5-position of the thiazole ring has a dihydrogen structure. The hydrogenation state changes the electron cloud distribution and spatial configuration of the thiazole ring, which further affects the chemical activity and stability of the whole molecule.
    In summary, the chemical structure of (S) -4,5-dihydro-2- (6-hydroxybenzothiazole-2-yl) thiazole-4-carboxylic acid is connected and interacted with the ring system by different functional groups, which endows the compound with diverse chemical properties and potential application value, and may have broad research prospects in the fields of medicinal chemistry and materials science.
    What are the physical properties of (S) -4,5-dihydro-2- (6-hydroxybenzothiazol-2-yl) thiazole-4-carboxylic acid?
    (S) -4,5-dihydro-2- (6-hydroxybenzothiazole-2-yl) thiazole-4-carboxylic acid, this is an organic compound. Looking at its molecular structure, it is cleverly connected by benzothiazole and thiazole carboxylic acid. The benzothiazole part contains 6-hydroxy group, and the thiazole ring is connected with carboxyl group at 4 positions. This unique structure gives it a variety of physical properties.
    First of all, its appearance is usually white to light yellow solid powder, and the texture is delicate, like delicate sand, and it feels smooth to the touch. This compound exhibits a certain hydrophilicity because it contains polar groups such as carboxyl and hydroxyl groups. In water, although the dissolution is limited, it can also be partially dissolved, just like a small amount of salt into the water, and the solution is slightly acidic, which is due to the ionization of carboxyl groups.
    Talking about the melting point, it has been experimentally determined to be between 200 and 210 ° C. When heated to this temperature range, it is like ice and snow meeting warm sun, and gradually melts from solid to liquid. Its stability is also worthy of attention. Under normal environmental conditions, it is quite stable, just like a strong fortress, and it is not easy to react with common substances in the air, such as oxygen and carbon dioxide. However, in the case of strong acid and alkali environments, it is like being in a fragile castle in the wind and rain, and the molecular structure will be affected and chemical reactions will occur.
    From the perspective of spectral properties, in the infrared spectrum, the stretching vibration summit of the carboxyl group appears in a specific wavenumber range, which is like a unique signal identification, providing an important basis for identifying the compound. In addition, in the nuclear magnetic resonance spectrum, hydrogen atoms at different positions will show characteristic chemical shifts, like different music notes forming a beautiful melody, helping researchers to further analyze their molecular structure. The physical properties of this compound are of great significance to its application in chemical synthesis, drug development and other fields, just like the cornerstone of a high-rise building, laying the foundation for related research and applications.
    What are the synthesis methods of (S) -4,5-dihydro-2- (6-hydroxybenzothiazol-2-yl) thiazole-4-carboxylic acid?
    The synthesis of (S) -4,5-dihydro-2- (6-hydroxybenzothiazole-2-yl) thiazole-4-carboxylic acid is a key exploration in the field of organic synthesis. To prepare this substance, various paths can be followed.
    First, it can be started from a benzothiazole derivative with a specific structure. First, the hydroxyl group of 6-hydroxybenzothiazole is shielded with an appropriate hydroxyl protecting group to prevent it from being disturbed in subsequent reactions. Then, through nucleophilic substitution, a group containing a thiazole ring precursor is introduced. This step requires careful selection of the reaction solvent and base to promote the anterograde reaction and obtain a higher yield. For example, polar aprotic solvents, such as N, N-dimethylformamide, with weak bases such as potassium carbonate, may be effective.
    Second, thiazole-4-carboxylic acid derivatives can also be used as starting materials. After modification and transformation, 6-hydroxybenzothiazole-2-yl is introduced. In the meantime, it may involve arylation reactions to construct the connection between benzothiazole and thiazole rings. Among them, the aromatization reaction catalyzed by palladium may be a good choice. When suitable palladium catalysts, ligands and bases are used to control the reaction temperature and time, precise synthesis can be achieved.
    Or it can start from simple small molecules containing sulfur, nitrogen and oxygen atoms, and gradually build the target molecular structure through multi-step cyclization and functional group transformation. Although this method is complicated, the stereochemistry and functional group position of the product can be fine-tuned according to the needs.
    All this synthesis method has advantages and disadvantages. It needs to be carefully weighed and carefully selected according to various factors such as the availability of raw materials, the simplicity of reaction conditions, the purity and yield of the product, etc., in order to achieve the ideal synthesis effect.
    What are the application fields of (S) -4,5-dihydro-2- (6-hydroxybenzothiazol-2-yl) thiazole-4-carboxylic acid?
    (S) -4,5-dihydro-2- (6-hydroxybenzothiazole-2-yl) thiazole-4-carboxylic acid, which is an organic compound. Its application field is quite wide, in the field of medicinal chemistry, it is often the key intermediate of active pharmaceutical ingredients. Based on it, physicians have carefully developed many drugs with specific biological activities, or can be used for the treatment and prevention of diseases, but the specific efficacy depends on its role in drug structure and interaction with biological targets.
    In the field of materials science, it may be used to create new functional materials due to its own special chemical structure and properties. If it is specially treated and modified, it may endow materials with unique optical, electrical or thermal properties, contributing to the innovative development of materials science.
    Furthermore, in the field of organic synthetic chemistry, it is an important synthetic building block for chemists to build more complex organic molecules. Through various organic reactions, chemists can skillfully use its structural characteristics to synthesize organic compounds with special structures and functions, promoting the progress of organic synthetic chemistry.
    This compound has shown potential application value in many fields such as medicine, materials and organic synthesis, and is indeed a must-see in chemical research and industrial production.
    What is the market outlook for (S) -4,5-dihydro-2- (6-hydroxybenzothiazol-2-yl) thiazole-4-carboxylic acid?
    (S) -4,5-dihydro-2- (6-hydroxybenzothiazole-2-yl) thiazole-4-carboxylic acid. In the current market prospect, this compound is like hidden in a fog and has not yet been clarified.
    Looking at its characteristics, this compound has a unique chemical structure and may have potential uses in the field of medicinal chemistry. However, the current market is still in the stage of exploration and concealment.
    In the field of academic research, although some researchers have explored its pharmacological activity, the results have not yet reached maturity. Preclinical research may have begun to emerge, but there is still a long way to go before it can be truly transformed into practical drugs.
    In terms of industrial production, its synthesis process may pose challenges. To achieve large-scale production, it is necessary to optimize the synthesis route, increase productivity and reduce costs. This process is like sailing against the current, and many technical barriers need to be overcome.
    At the level of market demand, due to the lack of extensive application cases, the scale of demand is still difficult to estimate. However, with the progress of pharmaceutical research and development, if its significant efficacy can be confirmed, it may find a place in the market for drugs for specific diseases.
    To sum up, the market prospect of (S) -4,5-dihydro-2 - (6-hydroxybenzothiazole-2-yl) thiazole-4-carboxylic acid, although it contains hope, there are many thorns ahead, and it is necessary for scientific research and industry to work together to clear the clouds and clarify its true market value.