2 Thiophenecarboxylic Acid 3 Chloro
quinoline thiophene imidazole thiazole

2-Thiophenecarboxylic acid, 3-chloro-

Taiy Chemical

    Specifications

    HS Code

    638973

    Name 3 - chloro - 2 - thiophenecarboxylic acid
    Molecular Formula C5H3ClO2S
    Molar Mass 162.599 g/mol
    Appearance Solid (usually white to off - white)
    Melting Point 155 - 159 °C
    Solubility In Water Slightly soluble
    Pka Around 2.79
    Density Approx. 1.58 g/cm³
    Boiling Point Decomposes before boiling

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    General Information
    Where to Buy 2-Thiophenecarboxylic acid, 3-chloro- in China?
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    Frequently Asked Questions

    As a leading 2-Thiophenecarboxylic acid, 3-chloro- supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What are the chemical properties of 3-chloro-2-thiophenecarboxylic acid?
    Mercury diacetic acid, also known as mercury oxalic acid, has unique chemical properties.
    In mercury diacetic acid, mercury element presents a specific chemical valence state, which makes mercury diacetic acid exhibit unique activity in chemical reactions. From the perspective of redox, mercury in mercury diacetic acid can change in valence state under specific conditions. When encountering strong reducing agents, mercury ions may be reduced to metallic mercury, and mercury diacetic acid itself participates in the reaction as an oxidizing agent.
    Furthermore, the acetic acid radical group in mercury diacetic acid also affects its chemical properties. Acetate has certain nucleophilic properties, and in some reaction systems, it can react with other electrophilic reagents, such as nucleophilic substitution reactions. For example, if there are suitable halogenated hydrocarbons in the system, acetate may replace halogen atoms to form new organic compounds.
    In addition, mercury diacetic acid will undergo a certain degree of dissociation in aqueous solution. Although mercury diacetic acid is not a strong acid and alkali salt, it will partially ionize in water to produce mercury ions and acetate ions. This dissociation equilibrium is affected by factors such as pH and temperature of the solution. When the acidity of the solution increases, the hydrolysis of acetate will be inhibited, thereby affecting the existence form and reactivity of mercury diacetic acid in the solution.
    In the field of organic synthesis, mercury diacetic acid can sometimes be used as a special catalyst or reagent. Due to the special electronic structure and coordination ability of mercury ions, they can form specific complexes with certain organic molecules, thereby changing the reaction path and rate, and catalyzing specific organic reactions, exhibiting unique chemical properties and application value.
    What are the main uses of 3-chloro-2-thiophenecarboxylic acid?
    3 + - -2-pentanoacetic acid has important uses in a wide range of fields.
    In the field of synthesis, it is an important factor in the production of multiple compounds. Taking the synthesis of some painkillers as an example, 3 + - -2-pentanoacetic acid is a series of reversals, which can introduce specific chemicals and enhance the pain activity of the compounds. Its ability to accurately reverse the reaction, making the molecules of the compounds have ideal rationality, and relieving the pain of patients is of paramount importance.
    In terms of research, this compound also has outstanding performance. It can be used as a raw material for the synthesis of new types of chemicals. Through chemical repair, it can create a specific crop disease with efficient control effect. Due to its specialization, the synthesized chemical can cause various biological reactions, such as nuclear substitution and acylation, in a specific way, to achieve a good control effect, thus ensuring the health of crops and improving productivity.
    Furthermore, in the field of synthesis, 3 + -2-pentanoacetic acid is like a clever "spoon". It can provide a variety of chemical compounds. With the active groups such as atoms and acylates it contains, it can generate multiple biological reactions, such as nuclear substitution, acylation, etc., to build up various carbon-carbon and carbon-carbon atoms, expand the diversity of molecules, and provide a powerful tool for synthesizers to explore new molecules and functions.
    What are the synthesis methods of 3-chloro-2-thiophenecarboxylic acid?
    To prepare 3-bromo-2-butanoic acid, the following synthesis methods can be used:
    First, butanoic acid is used as the starting material, and bromine atoms are introduced by halogenation reaction. In a suitable solvent, such as dichloromethane, under the action of a suitable temperature and catalyst, butanoic acid and bromine undergoes a substitution reaction. The α-hydrogen of butanoic acid has a certain activity and can be replaced by bromine atoms. This process requires attention to the fine regulation of reaction conditions. If the temperature is too high or the bromine is excessive, it may cause the formation of polyhalogenated by-products.
    Second, it can be achieved through a series of reactions such as esterification, halogenation and hydrolysis. First, butanoic acid and alcohols, such as ethanol, are esterified under acid catalysis to form butanoic acid esters. This ester compound is relatively stable. Subsequent to the reaction with brominating reagents under specific conditions, such as N-bromosuccinimide (NBS), bromine atoms selectively replace α-hydrogen atoms. Subsequently, hydrolysis under basic or acidic conditions converts the ester group into a carboxyl group to obtain 3-bromo-2-butanoic acid.
    Third, start with the construction of the carbon skeleton from the raw material and the introduction of functional groups. For example, the carbon chain is constructed by a reaction such as hydroxyaldehyde condensation with suitable alters and ketones and carboxyl-containing compounds, and then bromine atoms are introduced through steps such as halogenation. Although there are many steps in this approach, it can be flexibly designed according to the availability of raw materials and the feasibility of reaction conditions. For example, acetone and diethyl oxalate are used as the starting materials, through a series of reactions such as condensation, hydrolysis, decarboxylation, etc. Butanoic acid analogues are generated, and then halogenated to obtain the target product.
    Synthesis methods have their own advantages and disadvantages, and need to be weighed according to various factors such as raw material cost, reaction conditions, yield and product purity, and choose the best one to use.
    What are the precautions for 3-chloro-2-thiophenecarboxylic acid in storage and transportation?
    For those with 3 + -2-tert-butylacetic acid, there is no need to pay attention to it when it is hidden away.
























    < Therefore, the place where the gas is dry, or supplemented by the gas is dry, to prevent the damage of moisture.
    It is also necessary to use a container with a corrosion-resistant material. The compound may have a certain degree of corrosion. If the container is not resistant, it is easy to cause leakage, which not only affects the material, but also stains the environment, and is safe for health.
    When it comes to the gas, the first thing to do is to fix the package. Wrap it with suitable materials to prevent the container from being damaged due to shocks and collisions on the way. The road is rough and the moving is careless, so that the package can be damaged and the material can be released.
    The environment of the tool is also appropriate. Keep it cool and dry, and the requirements of hiding are different. If there is any leakage, etc., you can quickly take appropriate measures, such as isolation, cleaning, neutralization, etc. according to the nature, so as to prevent harm. Therefore, in the storage of 3 + - 2-tert-butylacetic acid, you should pay attention to the general situation to ensure its safety and effectiveness.
    What is the market price of 3-chloro-2-thiophenecarboxylic acid?
    In today's world, the market for ethyl lactate in the sea is a commercial thing, and it fluctuates due to factors such as fluctuations. If you want to know about it, you can use the business conditions.
    Those who are in the sea, where there is a lot of land, have a lot of money in the land, and are guided by the method of extraction, the way of transportation, and the supply and demand. For example, the coastal area is not convenient, or it is slightly flat; and the land is not large, and the increase is low, or it is high. And if the weather is not good, the amount is small, the number of seekers is small, and the supply is small, and the supply is limited. On the contrary, if the amount is abundant, the market is low and the price is high, there will be a reduction.
    Ethyl lactate, as a chemical raw material, is also subject to multi-terminal control. If the raw materials required for synthesis are high, the cost of ethyl lactate will be reduced. The technology of production, if the new technology is promoted, the efficiency will be improved, and the cost may be reduced, which will also be reduced. In addition, the requirements of production and protection can affect the cost of production, which will affect the market.
    If you want to know the quality of the two cities, you can go to the level of business, or the business and experts of the industry, in order to get the help of the business.