4 Methoxy Benzo B Thiophene 2 Carboxylic Acid
quinoline thiophene imidazole thiazole

4-Methoxy-benzo[b]thiophene-2-carboxylic acid

Taiy Chemical

    Specifications

    HS Code

    682157

    Chemical Formula C10H8O3S
    Molar Mass 208.23 g/mol
    Appearance Solid (predicted)
    Boiling Point Estimated to be relatively high due to intermolecular forces
    Solubility In Water Low solubility, as it is an organic acid with a non - polar thiophene and aromatic ring
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Pka Value related to its carboxylic acid group, indicating its acidity strength
    Density Estimated based on similar compounds, density around 1.3 - 1.4 g/cm³

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    General Information
    Where to Buy 4-Methoxy-benzo[b]thiophene-2-carboxylic acid in China?
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    Frequently Asked Questions

    As a leading 4-Methoxy-benzo[b]thiophene-2-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 4-methoxybenzo [b] thiophene-2-carboxylic acid?
    The chemical structure of 4-methoxybenzyl [b] naphthalene-2-carboxylic acid is quite complex and delicate. The structure of this compound is based on the naphthalene ring. The naphthalene ring is an aromatic hydrocarbon ring fused by two benzene rings. It has a unique conjugate system, which endows the compound with certain stability and special chemical properties.
    is at the 2-position of the naphthalene ring, and is connected with a carboxyl group (-COOH). Carboxyl groups are common functional groups in organic chemistry and are acidic. They can participate in many chemical reactions, such as esterification and salt formation, which greatly affect the chemical activity and physical properties of the compound.
    In the 4-position of the naphthalene ring, methoxybenzyl is connected. Among them, benzyl is benzyl (C H CH ² -), which has a certain stability and reactivity due to the conjugation effect of the benzene ring. And benzyl is connected with methoxy (-OCH 🥰), which is the power supply group. Through induction and conjugation effects, it affects the electron cloud distribution of the whole molecule, and then affects the reaction check point and reaction activity of the compound. < Br >
    The overall structure of methoxybenzyl [b] naphthalene-2-carboxylic acid, the interaction of various parts, endows the compound with unique physical and chemical properties, and may have important applications and research values in organic synthesis, medicinal chemistry and other fields.
    What are the main uses of 4-methoxybenzo [b] thiophene-2-carboxylic acid?
    4-Methylaminobenzo [b] thiazole-2-carboxylic acid, which has a wide range of uses. In the field of medicine, it is a key intermediate in the synthesis of many drugs. Due to its unique chemical structure, it can participate in the construction of molecular structures with specific pharmacological activities. For example, in the development of antibacterial drugs, its structural modification can enhance the inhibitory or killing ability of drugs against specific bacteria; in the exploration of anti-tumor drugs, or by combining with other active groups, new drugs with targeted effects on tumor cells can be designed.
    In the field of materials science, it also has its uses. It can be used to prepare functional polymer materials and endow materials with special optical and electrical properties. If it is treated by a special process, the polymer material containing this component exhibits unique fluorescence characteristics, which may have important applications in the field of optical sensors, can keenly perceive changes in specific substances or physical quantities, and is presented in the form of fluorescence signals.
    In organic synthetic chemistry, it is often used as an important starting material or reaction intermediate. With its active reaction check point, through various organic reactions, such as nucleophilic substitution, addition reaction, etc., numerous organic compounds with rich structures are derived, providing diverse possibilities for the development of organic synthetic chemistry, and helping chemists create more novel and unique organic molecules.
    What are the physical properties of 4-methoxybenzo [b] thiophene-2-carboxylic acids?
    4-Methoxybenzyl [b] quinoline-2-carboxylic acid is an organic compound with unique physical properties, which are described as follows:
    1. ** Appearance properties **: Usually in the state of white to light yellow crystalline powder. This appearance characteristic is convenient for preliminary identification and judgment in experiments and production. Due to different purity and crystallization conditions, the appearance may be slightly different, but it is mostly in the category of white to light yellow powder.
    2. ** Melting point Boiling point **: The melting point is about [X] ° C, and the boiling point is about [X] ° C under specific pressure. The melting point is of great significance for the identification of compounds, and the purity of the substance can be judged by melting point determination. If the purity is high, the melting point range is narrow and close to the theoretical value; if it contains impurities, the melting point decreases and the melting range becomes wider. The boiling point is related to the separation and purification of the substance, and it is separated from other substances by distillation and other means according to the difference in boiling point.
    3. ** Solubility **: Slightly soluble in water, easily soluble in common organic solvents, such as ethanol, dichloromethane, acetone, etc. This solubility makes it possible to choose a suitable organic solvent as the reaction medium according to the reaction requirements to ensure the smooth progress of the reaction. During separation and purification, the difference in solubility can also be used to separate it from the mixture by extraction and other operations.
    4. ** Density and stability **: The density is about [X] g/cm ³. Under normal conditions, the compound has certain stability, but when it encounters strong oxidants, strong acids, and strong bases, it may undergo chemical reactions to cause structural changes. High temperature and high humidity environments may also affect its stability, so it should be stored in a cool, dry, well-ventilated place away from incompatible substances.
    What are the synthesis methods of 4-methoxybenzo [b] thiophene-2-carboxylic acid?
    To prepare 4-methoxybenzo [b] thiophene-2-carboxylic acid, the method is as follows:
    First, start with 4-methoxybenzo [b] thiophene, and introduce an acyl group through acylation. If a suitable acylating agent is used, under suitable reaction conditions, the acyl group is attached to a specific position of the benzothiophene ring. Then the acyl group is oxidized to convert it to a carboxyl group. This oxidation step can be selected from a suitable oxidizing agent, such as potassium permanganate, etc., and react under appropriate reaction systems, such as suitable solvents, temperatures, etc., to obtain the target 4-methoxybenzo [b] thiophene-2-carboxylic acid.
    Second, the benzothiophene ring system can be constructed by condensation reaction from suitable raw materials containing sulfur and benzene rings. For example, the benzothiophene structure is formed by condensation of o-halogenated benzoic acid and sulfur-containing compounds in the presence of bases and catalysts. After that, the obtained product is methoxylated and modified. Suitable methoxylating reagents can be selected to introduce methoxy groups under suitable reaction conditions. Finally, through carboxylation reaction, a carboxyl group is introduced at the 2-position of the benzothiophene ring to synthesize 4-methoxybenzo [b] thiophene-2-carboxylic acid.
    Third, a compound with a similar structure is used as a raw material and converted into a functional group. For example, benzothiophene derivatives containing appropriate substituents are first introduced into the methoxy group through a substitution reaction, and then other suitable functional groups are converted into carboxyl groups through a series of reactions. For example, if the raw material contains oxidizable functional groups, the carboxyl group is obtained through oxidation reaction; or by reacting with carboxyl-containing reagents, through substitution, rearrangement and other steps, 4-methoxybenzo [b] thiophene-2-carboxylic acid is finally synthesized.
    What is the price range of 4-methoxybenzo [b] thiophene-2-carboxylic acid in the market?
    In the Wuguan market, the price of 4-methoxybenzyl [b] naphthylamine-2-carboxylic acid varies depending on various factors such as quality, source, and season.
    Generally speaking, if its quality is high and the source is orthodox, in the medicinal herb industry or in the general professional market, the price per tael may be between ten and thirty taels of silver. However, if the quality is slightly inferior, or the source is mixed, the price may be reduced to fifty to fifteen taels of silver per tael.
    And in different places, the price also varies. In most prosperous cities, due to the large demand, merchants gather, and the price may be slightly higher; in remote towns, the demand is weak, and the supply is also small, and the price may be slightly lower.
    Furthermore, the change of season also affects its price. When new products are listed, the supply is sufficient, and the price may stabilize and decline; while when the supply is scarce, the price may rise.
    Therefore, to know the exact price, you need to go to the market in person and consult all merchants in detail before you can get it.