3 Bromo 2 Thiophenecarboxylic Acid
quinoline thiophene imidazole thiazole

3-Bromo-2-thiophenecarboxylic acid

Taiy Chemical

    Specifications

    HS Code

    193836

    Chemical Formula C5H3BrO2S
    Molar Mass 209.04 g/mol
    Appearance Solid (usually white to off - white)
    Melting Point 138 - 142 °C
    Solubility In Water Slightly soluble
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Acidity Weakly acidic due to carboxylic acid group
    Stability Stable under normal conditions, but can react with strong bases, oxidizing agents
    Odor Odorless or very faint odor

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    General Information
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    Frequently Asked Questions

    As a leading 3-Bromo-2-thiophenecarboxylic 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 chemistry of 3-Bromo-2-thiophenecarboxylic acid?
    3-Bromo-2-thiophenecarboxylic acid is one of the organic compounds. Its appearance is often white to light yellow crystalline powder. This substance is acidic, because it contains carboxyl groups, it can react with bases to form corresponding carboxylic salts. In the field of organic synthesis, this is a key intermediate.
    In terms of physical properties, the melting point is about 168-172 ° C. This melting point characteristic is very important for the purification and identification of compounds. Due to the different melting points of different compounds, its purity and authenticity can be preliminarily determined by accurately measuring the melting point.
    In terms of chemical properties, in addition to the acidic reaction of carboxyl groups, bromine atoms also give it unique activity. Bromine atoms can participate in many substitution reactions, such as nucleophilic substitution. In such reactions, bromine atoms can be replaced by other nucleophilic reagents, thereby constructing new organic compound structures and expanding the path of organic synthesis.
    In addition, the presence of thiophene rings makes molecules aromatic, affecting their electron cloud distribution and reactivity. Thiophene rings can undergo electrophilic substitution reactions, and the reactivity at specific locations is different, which provides the possibility for the synthesis of complex organic molecules.
    When storing, pay attention to its stability. Due to its certain chemical activity, it should be stored in a cool, dry, and well-ventilated place, away from fire sources and oxidants, to prevent accidental chemical reactions and ensure its chemical stability for subsequent use in organic synthesis.
    What are the main uses of 3-Bromo-2-thiophenecarboxylic acid?
    3-Bromo-2-thiophenecarboxylic acid has a wide range of uses. It is a key intermediate in the field of pharmaceutical synthesis. In the process of drug development, it can be converted into compounds with specific pharmacological activities through specific chemical reactions, which can be used to treat various diseases.
    In the creation of pesticides, 3-bromo-2-thiophenecarboxylic acid is also indispensable. Through ingenious chemical modification and synthesis paths, highly efficient and low-toxic pesticides can be prepared, which have significant control effects on crop diseases and pests, can effectively improve the yield and quality of crops, and ensure the stable development of agriculture.
    In the field of materials science, it also shows unique value. With its own chemical structure characteristics, it can participate in the synthesis of materials with special properties, such as some organic materials with specific photoelectric properties, which have potential application prospects in electronic devices, optical equipment and other fields.
    In addition, in the study of organic synthetic chemistry, 3-bromo-2-thiophenecarboxylic acid is often used as a basic raw material for researchers to explore and study various novel chemical reactions, and to promote the continuous progress and development of organic synthesis methodologies. In short, it plays an important role in many fields and has a positive and far-reaching impact on the development of related industries.
    What are the synthetic methods of 3-Bromo-2-thiophenecarboxylic acid?
    3-Bromo-2-thiophenecarboxylic acid has been synthesized in ancient times, and there are various ways.
    First, 2-thiophenecarboxylic acid is used as the starting material and prepared by bromination reaction. This process requires careful selection of suitable brominating reagents, such as liquid bromine, N-bromosuccinimide (NBS), etc. If liquid bromine is used, its reactivity is high, so it is necessary to pay attention to the precise control of the reaction conditions, such as temperature and solvent selection. Usually, the reaction can proceed smoothly at low temperature and in the presence of suitable catalysts. When NBS is selected, the reaction conditions are relatively mild and easy to control. In an organic solvent, such as carbon tetrachloride, the bromination of 2-thiophenecarboxylic acid can be achieved under the action of light or an initiator, and the target product is 3-bromo-2-thiophenecarboxylic acid.
    Second, you can start from thiophene. First, the thiophene is acylated, and the carboxyl group is introduced into the prototype, and then the bromination step is carried out. The acylation reaction can use suitable acylation reagents and catalysts, such as anhydrous aluminum trichloride, to react with the corresponding acyl halogen. The subsequent bromination is based on the above-mentioned similar method, and the appropriate brominating reagents and conditions are selected to realize the transition to 3-bromo-2-thiophenecarboxylic acid.
    Third, other compounds containing thiophene structures are also used as starters and synthesized through multi-step reactions. First, the starter is modified and transformed with specific functional groups to construct a structure close to the target product, and then through the key bromination and carboxylation steps, the final product is 3-bromo-2-thiophenecarboxylic acid. Although this approach is slightly complicated, the synthesis route can be flexibly adjusted according to the availability of raw materials and the selectivity of the reaction to achieve the purpose of efficient synthesis.
    What is the market price of 3-Bromo-2-thiophenecarboxylic acid?
    3-Bromo-2-thiophenecarboxylic acid, the market price of this product, it is difficult to say in a word. Prices in the city often fluctuate due to changes in time, place, quality and supply and demand.
    In the past, in the market of chemical raw materials, the price was always determined by supply and demand. If there are many people in need and few producers, the price will rise; on the contrary, if the supply exceeds the demand, the price may fall.
    Looking at the past market, when the raw materials are abundant and the output is stable, the price is still stable. However, if raw materials are scarce or production is blocked, such as natural disasters, man-made disasters, policy changes affecting the supply of upstream raw materials, or production processes are difficult to innovate, resulting in higher costs, the price will also fluctuate.
    And in different places, the price is also different. Prosperous commercial ports, smooth transportation, convenient logistics, their price may be easier due to competition; remote places, inconvenient transportation, cost superposition, price may be slightly higher.
    And product quality is also related to price. Those with high purity and few impurities are often better than those with inferior quality.
    To sum up, in order to know the current market price of 3-bromo-2-thiophenecarboxylic acid, it is advisable to consult chemical raw material distributors, trading platforms, or visit the chemical market in person, in order to obtain a certain number. It is absolutely impossible to measure its price at one end.
    What to pay attention to when storing and transporting 3-Bromo-2-thiophenecarboxylic acid
    3-Bromo-2-thiophenecarboxylic acid, this is an organic compound. When storing and transporting, many things need to be paid attention to.
    Bear the brunt. When storing, choose a cool, dry and well-ventilated place. This compound is easy to decompose and deteriorate when heated, so it needs to be kept away from heat sources and fires. If placed in a high temperature environment, it may cause chemical reactions, resulting in damage to its quality or even danger.
    Furthermore, it is quite sensitive to humidity, which can easily cause reactions such as hydrolysis to affect its quality. Therefore, the storage container must be tightly sealed to prevent moisture from invading. Sealed containers such as glass bottles or metal drums lined with plastic can be used.
    In terms of transportation, caution is also required. It should be ensured that the means of transportation are clean and dry, and there are no other substances that may react with them. And during transportation, severe vibrations and collisions should be avoided to prevent the container from breaking and causing the compound to leak.
    Because it is a chemical, transportation and storage must follow relevant regulations and standards. Operators should have professional knowledge and be familiar with the characteristics of the compound and emergency treatment methods. In the event of an accident such as leakage, it can be disposed of quickly and properly to prevent the expansion of the hazard.
    In addition, storage places and transportation vehicles should also be equipped with corresponding fire protection and leakage emergency treatment equipment, such as fire extinguishers, adsorption materials, etc., for emergency needs. Only in this way can the safety and quality of 3-bromo-2-thiophenecarboxylic acid be ensured during storage and transportation.