Ethyl 2 Amino Alpha Hydroxyimino 4 Thiazoleacetate
quinoline thiophene imidazole thiazole

Ethyl 2-amino-alpha-(hydroxyimino)-4-thiazoleacetate

    Specifications

    HS Code

    265687

    Chemical Formula C7H9N3O4S
    Molecular Weight 231.23 g/mol
    Appearance White to off - white crystalline powder
    Solubility In Water Poorly soluble
    Solubility In Organic Solvents Soluble in some polar organic solvents like methanol, ethanol
    Melting Point 160 - 163 °C
    Purity Typically high - purity products are around 98% or higher
    Odor Odorless or very faint odor
    Stability Stable under normal conditions, but sensitive to strong acids and bases

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    General Information
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    Frequently Asked Questions

    As a leading Ethyl 2-amino-alpha-(hydroxyimino)-4-thiazoleacetate 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 Ethyl 2-amino-alpha- (hydroxyimino) -4-thiazoleacetate?
    Ethyl + 2 - amino - alpha - (hydroxyimino) - 4 - thiazoleacetate is 2 - amino - α - ( hydroxyimino) - 4 - thiazolium ethyl acetate, its chemical structure is as follows.
    The core structure of this compound is a thiazole ring, which is a five-membered heterocyclic structure composed of a sulfur atom and a nitrogen atom in adjacent positions. At position 4 of the thiazole ring, an ethyl acetate group is connected. In the ethyl acetate group, the ethyl ester group is connected by an ethyl group to the carbonyl group, and the carbonyl group is connected to the carboxyl group of the acetic acid. An oxygen atom in this carboxyl group is connected to the thiazole ring at position 4 in the form of a single bond.
    An amino group is connected at position 2 of the thiazole ring. And a hydroxyimino group is connected to the α position of the acetic acid group connected to position 4 of the thiazole ring (that is, the carbon atom directly connected to the carboxyl group). The hydroxyimino group is connected by a hydroxyl group to the imino group, and the imino group is connected to the α-carbon atom through the nitrogen atom.
    Overall, the compound is composed of a thiazole ring as the core, which is connected to a side chain with specific functional groups, including amino groups, hydroxyimino groups, and ethyl acetate groups, which together constitute Ethyl + 2 - amino - alpha - (hydroxyimino) - 4 - thiazoleacetate unique chemical structure, different functional groups endow the compound with specific chemical properties and reactivity.
    What are the main uses of Ethyl 2-amino-alpha- (hydroxyimino) -4-thiazoleacetate?
    Ethyl + 2 - amino - alpha - (hydroxyimino) -4 - thiazoleacetate is 2 - amino - α - ( hydroxyimino) - 4 - thiazoleacetate ethyl acetate, which has a wide range of uses.
    In the field of medicine, it is a key intermediate for the synthesis of cephalosporins. Many such antibiotics, such as cefoxime and cefodil, rely on this material for their preparation. By reacting with other compounds, the core structure of antibiotics can be constructed. These antibiotics have broad-spectrum antibacterial effects and can respond to a variety of bacterial infections, such as respiratory tract infections, urinary tract infections, etc., and make great contributions to the treatment of human diseases. < Br >
    In the field of pesticides, it is also important. It can be converted into compounds with bactericidal and insecticidal activities through specific reactions. Such pesticides can effectively prevent and control crop diseases and pests, ensure crop growth, improve crop yield and quality, and help agricultural production.
    In the field of organic synthetic chemistry, as a compound with a unique structure, it can be used as a building block for organic synthesis. Chemists can create organic compounds with diverse structures and specific properties by modifying and transforming their functional groups, laying the foundation for the research and development of new drugs and new materials, and promoting the continuous development of organic synthetic chemistry.
    What is the preparation method of Ethyl 2-amino-alpha- (hydroxyimino) -4-thiazoleacetate?
    The ancient method of preparing ethyl 2-amino-alpha-4-thiazoleacetate has also been traced. 2-Amino-4-thiazoleacetic acid is often used as the starting material, and it is first reacted with appropriate reagents to form an ester. For example, ethyl 2-amino-4-thiazoleacetate can be obtained by esterification of ethanol and acid under the action of a catalyst.
    Then, to introduce the structure of alpha- (hydroxyimino), suitable oximizing reagents are often used to react with it. Common oximing reagents, such as hydroxylamine hydrochloride, are mixed with the above-mentioned esterides under appropriate reaction conditions. The pH, temperature and reaction time of the reaction system are all key factors.
    Usually, the reaction system is adjusted to a suitable alkalinity so that hydroxylamine hydrochloride can participate in the reaction in a suitable form. The temperature may be controlled within a moderate range, such as heating to tens of degrees Celsius, for a period of time to allow the reaction to proceed fully. During this period, the oximizing reagent reacts with the α-site carbonyl group of the esteride to gradually form an α- (hydroxyimino) structure, and finally ethyl 2-amino-α- (hydroxyimino) -4-thiazole acetate is obtained. Although there are many steps in this preparation method, the compound can be obtained by following appropriate reaction conditions and operations.
    What are the physicochemical properties of Ethyl 2-amino-alpha- (hydroxyimino) -4-thiazoleacetate
    Ethyl + 2 - amino - alpha - (hydroxyimino) - 4 - thiazoleacetate, the Chinese name is often referred to as 2 - amino - α - ( hydroxyimino) - 4 - thiazole ethyl acetate, the physical and chemical properties of this substance are as follows:
    View, under normal temperature, it is mostly white to light yellow crystalline powder, its shape is delicate, uniform texture, eyesight view, no obvious impurities mixed in it.
    Smell, this substance has little smell, no strong pungent smell, only a very light special smell, placed under the nose to smell, can be detected.
    As for the melting point, it is about 120-125 ° C. When the temperature gradually rises to the vicinity of the melting point, it gradually melts from solid to liquid, and this process is clearly observable. In this temperature range, the thermal movement of the substance molecules intensifies, the lattice structure is gradually destroyed, and the phase state transition occurs.
    In terms of solubility, it exhibits good solubility in organic solvents such as methanol and ethanol. Taking ethanol as an example, if an appropriate amount of the substance is placed in ethanol and stirred slightly, it can be seen slowly dissolving to form a uniform solution. However, in water, its solubility is poor, and although it is stirred for a long time, there are still more substances that sink to the bottom of the water and are difficult to dissolve. This is because in the molecular structure of the substance, there are both groups that interact with organic solvents and parts that interact weakly with water, so there is such a difference in solubility.
    Its chemical stability is quite stable under normal mild conditions. However, in the case of strong acid, strong alkali environment, or extreme conditions such as high temperature and high humidity, its chemical structure is easily damaged. For example, if it is placed in a strong acid solution, after a period of time, it can be found by chemical analysis that some chemical bonds in its molecular structure have broken and new chemical substances have been formed, which shows its sensitivity to a specific chemical environment.
    Ethyl 2-amino-alpha- (hydroxyimino) -4-thiazoleacetate during use
    Fuethyl - 2 - amino - α -( hydroxyimino) - 4 - thiazole acetate, when using, there are a number of things to pay attention to, need to pay attention to.
    First, this material has a specific chemical activity, so when storing, it must be placed in a dry, cool and well ventilated place. If placed in a humid and warm place, it may cause its chemical properties to change and affect its effectiveness. And it needs to be separated from oxidizing agents, acids, bases and other substances to prevent dangerous chemical reactions.
    Second, during use, the operator must strictly abide by safety procedures. Appropriate protective equipment such as protective clothing, gloves and goggles should be worn. Because it may be irritating to the skin, eyes and respiratory tract. If you accidentally contact the skin, you should immediately rinse with a lot of water. If you contact the eyes, you need to rinse with flowing water quickly and seek medical treatment in time.
    Furthermore, when measuring and using, it is necessary to operate with precision. Due to its special chemical properties, the amount of dosage has a great impact on the reaction result. Slight deviation, or the reaction is not as expected, or unexpected side reactions. And the equipment used should also be clean and dry to avoid the introduction of impurities and interfere with the reaction process.
    Also, after use, the remaining materials and waste should not be discarded at will. It needs to be properly disposed of in accordance with relevant regulations. Because of its potential harm to the environment, environmental protection requirements should be followed to ensure that the surrounding environment is not polluted.
    In general, the use of ethyl - 2 - amino - α -( hydroxyimino) - 4 - thiazole acetate should be used with caution, pay attention to the above things, in order to ensure the safety and effect of use.