4 Bromo 1 3 Thiazole 2 Carboxaldehyde
quinoline thiophene imidazole thiazole

4-Bromo-1,3-thiazole-2-carboxaldehyde

    Specifications

    HS Code

    528505

    Chemical Formula C4H2BrNOS
    Molecular Weight 192.03 g/mol
    Appearance Solid (usually)
    Melting Point Data - specific value needed
    Boiling Point Data - specific value needed
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane
    Density Data - specific value needed
    Flash Point Data - specific value needed
    Purity Can be high - purity (e.g., 95%+ in some cases)
    Chemical Reactivity Reactive towards nucleophiles due to aldehyde group

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    General Information
    Where to Buy 4-Bromo-1,3-thiazole-2-carboxaldehyde in China?
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    Frequently Asked Questions

    As a leading 4-Bromo-1,3-thiazole-2-carboxaldehyde supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    4-Bromo-1, what are the chemical properties of 3-thiazole-2-carboxaldehyde
    4-Bromo-1,3-thiazole-2-formaldehyde, this is an organic compound. Looking at its structure, the thiazole ring is the group, the bromine atom is at the 4th position, and the aldehyde group is at the 2nd position. Its chemical properties are unique and interesting. The presence of the
    aldehyde group gives it significant chemical activity. The aldehyde group has strong reducing properties and can react with many oxidants. For example, when interacted with weak oxidants such as Torun reagent (silver ammonia solution), a silver mirror reaction can occur. The aldehyde group is oxidized to a carboxyl group to precipitate metallic silver, such as forming a beautiful silver mirror on the inner wall of a clean test tube. The reaction with Feilin reagent can also reduce the blue copper ions to form a brick-red cuprous oxide precipitate. The characteristics of the
    bromine atom cannot be ignored. Because the bromine atom has electron-absorbing properties, it affects the electron cloud distribution of the thiazole ring, which in turn changes the reactivity of the molecule. This bromine atom can participate in nucleophilic substitution reactions, such as substitution with nucleophilic reagents such as alcohols and amines, to form new organic compounds, thereby expanding the derivatization path of the substance. The
    thiazole ring itself is a five-membered heterocycle containing sulfur and nitrogen, which endows the compound with certain stability and unique electronic effects. The electron cloud distribution on the ring is more complex due to the existence of bromine and aldehyde groups, which makes this substance a key intermediate in the field of organic synthesis, participating in the construction of many complex organic molecules, providing rich possibilities and broad application prospects for the creation of novel and specific functional organic compounds.
    What are the common synthesis methods of 4-Bromo-1, 3-thiazole-2-carboxaldehyde
    4-Bromo-1,3-thiazole-2-formaldehyde is also an important intermediate in organic synthesis. There are various common synthesis methods, and each has its own advantages and disadvantages, which are described in detail below.
    First, based on thiazole ring, obtained by bromination and formylation. First, take a suitable thiazole derivative, use a brominating agent, such as bromine or N-bromosuccinimide (NBS), in a suitable solvent, such as dichloromethane or carbon tetrachloride, control the reaction temperature and time to bromide the thiazole ring at a specific position. Then, the formylation reaction is carried out with formylation reagents, such as Vilsmeier-Haack reagent composed of DMF and phosphorus oxychloride (POCl 🥰). This process requires attention to the dosage of reagents and reaction conditions to avoid side reactions. For example, the temperature during bromination is too high, which may lead to polybrominated products; the proportion of reagents during formylation is improper, which also affects the yield and purity.
    Second, it is prepared by cyclization with a raw material containing bromine and an aldehyde group. For example, β-aminothiol containing bromine and a suitable carbonyl compound are cyclized and condensed under acidic or basic catalysis to obtain the target product. Acetic acid or hydrochloric acid are commonly used in acidic catalysis, and sodium hydroxide or potassium carbonate are used in alkaline catalysis. This path requires a suitable raw material ratio and reaction environment to promote the smooth progress of cyclization. If the proportion of raw materials is unbalanced or the cyclization is incomplete, the product is complex and difficult to separate.
    Third, it is converted from other thiazole derivatives. Some thiazole compounds with specific substituents can be synthesized by 4-bromo-1,3-thiazole-2-formaldehyde after functional group transformation, such as oxidation, reduction, and substitution of specific groups. This approach requires a deep understanding of the reaction mechanism, and careful design of reaction steps according to the characteristics of raw materials and the structure of target products.
    All such synthesis methods need to be based on actual conditions, such as raw material availability, cost, equipment conditions, etc., to weigh the advantages and disadvantages and choose the best method to achieve high-efficiency and high-purity synthesis.
    4-Bromo-1, 3-thiazole-2-carboxaldehyde in which areas
    4-Bromo-1,3-thiazole-2-formaldehyde, which is used in various fields such as medicine, pesticides and materials science.
    In the field of medicine, it can be used as a key intermediate for the synthesis of various drugs. The unique chemical properties of the thiazole ring and aldehyde group can be combined with many biologically active molecules. For example, in the creation of antibacterial drugs, 4-bromo-1,3-thiazole-2-formaldehyde can be linked to specific antibacterial groups through a series of chemical reactions to develop new antibacterial agents to deal with the challenge of drug-resistant bacteria.
    In the field of pesticides, it also plays an important role. It can be used as a raw material for the synthesis of high-efficiency and low-toxicity pesticides. Using it as a starting material, through clever chemical transformation, pesticides with high selectivity to pests and environmental friendliness can be prepared, which can help the green development of agriculture and ensure crop yield and quality.
    In the field of materials science, 4-bromo-1,3-thiazole-2-formaldehyde can participate in the preparation of special materials. It can be polymerized with other organic or inorganic monomers to generate materials with special optical, electrical or mechanical properties. For example, the preparation of photoelectric functional materials can be applied to cutting-edge technologies such as organic Light Emitting Diode and solar cells to promote the progress of materials science.
    What is the market price of 4-Bromo-1,3-thiazole-2-carboxaldehyde?
    The price of 4-bromo-1,3-thiazole-2-formaldehyde in the market is difficult to determine. Its price often changes due to many reasons, such as the trend of supply and demand, the difficulty of preparation, the difference in quality, and even the change of luck.
    Looking at the city of the past, when the supply and demand of materials were in balance, the price was still stable. However, if there are many people in need and few suppliers, the price will increase; otherwise, it may decrease. And if the preparation method is complex, the consumables are laborious, and the cost will be high, the price in the market will also rise accordingly. Furthermore, those with high quality are often more expensive than usual.
    In addition, changes in luck also affect its price. If the current situation is stable and business is smooth, the price may be flat; in case of disasters, wars, or changes in government orders, materials are scarce, transportation is difficult, and the price fluctuates.
    Although it is difficult to know the exact price, according to past cases and market conditions, the price changes with changes in the market, with few gold, many or dozens of gold, or even more, it is difficult to determine, and it needs to be carefully studied in the city to obtain a real-time price.
    4-Bromo-1, what are the storage conditions for 3-thiazole-2-carboxaldehyde
    4-Bromo-1,3-thiazole-2-formaldehyde is an extremely delicate chemical substance. Its preservation method requires careful attention to ensure its quality.
    The first dry environment. This substance is very easy to contact with water vapor and deteriorate. Therefore, when placed in a place with extremely low humidity, it can be surrounded by a desiccant, such as silica gel, to absorb the surrounding water vapor and make the environment dry and clean. It is like being placed in the hinterland of a desert without the intrusion of water vapor.
    The second is temperature control. It should be stored in a low temperature place, usually 2-8 ° C, just like being placed in a cool cave, with a constant and cool temperature. Do not place it in high temperature or direct sunlight, because high temperature will accelerate its chemical reaction, and various rays in sunlight will also cause its structure to mutate, causing it to lose its original properties.
    Furthermore, tight packaging is indispensable. When it is in a well-sealed container, such as a glass bottle, and the mouth of the bottle must be tightly closed to prevent a trace of air from taking advantage of it. This is like building an indestructible fortress for it, outside air and impurities are not allowed to enter, so as to keep it pure as before.
    Also pay attention to avoid mixing with other chemicals. Because of its chemical activity, if it coexists with unsuitable substances, it may cause violent reactions and damage its quality. When storing, be sure to isolate it from other things and keep it in a separate place, just like a gentleman alone, not flowing with turbid matter.
    Such various preservation conditions must be carefully observed in order to keep 4-bromo-1,3-thiazole-2-formaldehyde in its quality for a long time, and it will play its due role in subsequent use.