Z 2 2 Aminothiazole 4 Yl 2 Methoxycarbonylmethoxy Imino Acetic Acid
quinoline thiophene imidazole thiazole

(Z)-2-(2-Aminothiazole-4-yl)-2-(methoxycarbonylmethoxy-imino) acetic acid

    Specifications

    HS Code

    436839

    Chemical Formula C10H11N3O5S
    Molecular Weight 285.28
    Appearance Solid (usually white to off - white)
    Melting Point Data may vary, typically in a certain temperature range
    Solubility Solubility characteristics in different solvents like water, organic solvents
    Pka Value Value related to its acidic - basic properties
    Stability Thermal, chemical stability details
    Odor May have a characteristic odor or be odorless
    Crystal Structure Details of its crystal lattice if known
    Reactivity Reactivity with common reagents

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    General Information
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    Frequently Asked Questions

    As a leading (Z)-2-(2-Aminothiazole-4-yl)-2-(methoxycarbonylmethoxy-imino) acetic 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 (Z) -2- (2-aminothiazole-4-yl) -2- (methoxycarbonyl methoxy-imino) acetic acid?
    What is the chemical structure of (Z) - 2 - (2 - hydroxyvaleraldehyde - 4 - yl) - 2 - (methoxymethoxy - hydroxylidene) acetic acid? And please imitate "Tiangong Kaiwu" to answer this question in classical Chinese format.
    Fuzhuming (Z) - 2 - (2 - hydroxyvaleraldehyde - 4 - yl) - 2 - (methoxymethoxy - hydroxylidene) acetic acid The chemical structure of its components needs to be investigated in detail.
    The first word " (2-hydroxyvaleraldehyde-4-yl) ", valeraldehyde, is a pentacarbon aldehyde compound. The aldehyde group is the functional group at one end, and the 2-position hydroxyl group is added, and the 4-position is part of the compound connected elsewhere.
    The second view " (methoxy methoxy-hydroxylidene) ", methoxy, is the group connected to the methyl group and the oxygen group. Here there are two methoxy groups combined with hydroxylidene. hydroxylidene, a hydroxyl group with one less hydrogen atom.
    As for this acetic acid, the structure of glycolic acid is the group, and the carboxyl group is its significant functional group.
    Overall, the structure of (Z) -2- (2-hydroxyvaleraldehyde-4-yl) -2- (methoxymethoxy-hydroxylidene) acetic acid, with acetic acid as the main body, is connected at 2 positions (2-hydroxyvaleraldehyde-4-yl) and (methoxymethoxy-hydroxylidene). In its spatial structure, each atom is connected to each other by the force of chemical bonds to form this unique chemical structure. The carbon chain skeleton is arranged in sequence, and each functional group interacts at a specific position with its inherent chemical properties, so that this compound has specific chemical activities and physical properties. Although it is difficult to express its three-dimensional delicate structure in words, a rough outline of its chemical structure can be obtained based on this analysis.
    What are the main uses of (Z) -2- (2-aminothiazole-4-yl) -2- (methoxycarbonyl methoxy-imino) acetic acid?
    (Z) - 2 - (2 - hydroxypyridine - 4 - yl) - 2 - (methoxycarbonyl methoxy - hydroxylidene) acetic acid, although this compound was not recognized in modern times in "Tiangong Kaiwu", from an ancient perspective, the use of related substances can be speculated as follows.
    In the field of ancient medicine, many natural substances containing hydroxyl groups, carbonyl groups and other similar structures were often explored for medicinal value. If this substance was discovered at that time, doctors may observe its effects on human diseases based on experience and attempts. For example, traditional medicine often extracts ingredients from plants and minerals to treat diseases, and may try to relieve some heat toxicity and swelling and pain to see if it is equivalent to clearing away heat, detoxifying, and reducing swelling. However, due to the lack of modern scientific verification, the effect is difficult to accurately evaluate.
    In the ancient dyeing and weaving industry, some substances containing specific groups can be used as dyes or mordants. If this compound has some properties that can bind to fabrics and give color, it may be used in fabric dyeing to give fabrics a unique color and enhance the aesthetics and commercial value of fabrics. Like ancient times, various plant and mineral pigments were often used for dyeing, if this material can participate in it, or add new color options to the dyeing and weaving process.
    In ancient chemical exploration activities such as alchemy, alchemists were curious about all kinds of novel substances. They might include this compound in their alchemy experiments, hoping to obtain medicinal pills with magical effects through a special refining process. Although their knowledge and methods were unscientific, they reflected an attempt to excavate the properties of unknown substances.
    What are the synthesis methods of (Z) -2- (2-aminothiazole-4-yl) -2- (methoxycarbonyl methoxy-imino) acetic acid?
    There are many synthetic methods of (Z) - 2 - (2 - hydroxybutyraldehyde - 4 - yl) - 2 - (methoxycarbonyl methoxy - hydroxylidene) acetic acid, which are described in detail below.
    First, the target molecule can be gradually constructed through a multi-step reaction from the starting material. First, the aldehyde group is properly protected by a compound containing hydroxyl and aldehyde groups, and then the hydroxyl group is functionally converted, and a specific substituent is introduced to form a key intermediate. Subsequently, the protective group is removed, and through suitable reaction conditions, the intermediate is further reacted to construct a structural unit containing methoxycarbonyl methoxy-hydroxylene group. Finally, through condensation and other reactions, (Z) -2- (2-hydroxybutyraldehyde-4-yl) -2- (methoxycarbonyl methoxy-hydroxylene) acetic acid is synthesized.
    Second, the reverse synthesis analysis strategy can be adopted. The target molecule is reversely disassembled into several relatively simple precursors. Starting from the structural characteristics of the target molecule, consider cutting some chemical bonds to obtain possible intermediates. For example, the methoxycarbonyl methoxy-hydroxylene moiety is cut off from the main structure, and the corresponding fragments are synthesized separately, and then these fragments are spliced together through suitable ligation reactions, such as esterification, condensation, etc., to achieve the synthesis of the target compound.
    Third, we can also learn from the synthesis methods of similar structural compounds in the literature, and appropriately optimize and adjust the existing synthesis routes according to the structural differences of the target molecules. By changing the reaction conditions and selecting different reagents or catalysts, the reaction was more selective and efficient, and (Z) -2- (2-hydroxybutyraldehyde-4-yl) -2- (methoxycarbonyl methoxy-hydroxylidene) acetic acid was successfully synthesized. Each method has its own advantages and disadvantages, and it is necessary to comprehensively consider many factors such as the availability of raw materials, the difficulty of reaction conditions, cost and yield, and select the most suitable synthesis path.
    What are the physicochemical properties of (Z) -2- (2-aminothiazole-4-yl) -2- (methoxycarbonyl methoxy-imino) acetic acid?
    (Z) - 2 - (2 - hydroxybutyraldehyde - 4 - yl) - 2 - (acetoxy acetoxy - hydroxylidene) acetic acid, which is an organic compound with unique physical and chemical properties.
    In terms of physical properties, it is liquid under normal conditions and has certain fluidity. However, due to the molecular structure containing a variety of functional groups, the intermolecular force is complex, resulting in a higher boiling point, and more energy is required to overcome the intermolecular attractive force to achieve gasification. And because it contains polar hydroxyl and carbonyl functional groups, it may have a certain solubility in polar solvents (such as water, ethanol), but limited solubility in non-polar solvents (such as benzene, carbon tetrachloride).
    From the perspective of chemical properties, the hydroxyl groups in the molecule can undergo esterification reaction, and the corresponding esters can be formed with acids under the action of catalysts. This reaction is a common means of organic synthesis, which can change the properties and uses of compounds. Carbonyl groups are electrophilic and can undergo addition reactions with nucleophiles. For example, when reacted with Grignard reagents, carbon chains can grow and complex organic structures can be constructed. The acetoxy group part may be hydrolyzed under alkaline conditions or under alkaline conditions to form acetate ions and corresponding alcohols. This hydrolysis reaction may be of great significance in organic synthesis and metabolism in vivo. Hydroxylene groups also have certain reactivity and can participate in redox reactions, which affect the chemical transformation of compounds. In short, the physical and chemical properties of this compound make it potentially valuable in organic synthesis, medicinal chemistry and other fields.
    What are the market prospects for (Z) -2- (2-aminothiazole-4-yl) -2- (methoxycarbonyl methoxy-imino) acetic acid?
    (Z) - 2 - (2 - hydroxypyridine - 4 - yl) - 2 - (acetoxyacetoxy - hydroxylidene) acetic acid in the market, its scene is as follows:
    This compound in the market scene, related to many elements. First of all, its use, in the field of pharmaceutical research and development, or as a key intermediate, can be used to synthesize specific drugs, with therapeutic effect on specific diseases, if it can be successfully developed and approved for marketing, the market demand may be considerable due to the number of patients with symptoms. In the chemical industry, or as raw materials for the preparation of special materials, if the relevant materials have unique applications in high-tech industries, such as electronics, aerospace and other fields, their market prospects will also be bright.
    However, its market prospects also pose challenges. From a competitive perspective, if similar compounds are already available in the industry and the technology is mature, new entrants need to demonstrate their advantages in terms of performance and cost if they want to seize market share. Furthermore, regulations and policies strictly regulate chemical and pharmaceutical products, and their production, sales and use need to follow complicated regulations. If they fail to meet the requirements, the products will be difficult to market and circulate.
    In addition, market dynamics and consumer preferences also affect their prospects. If the market demand for green and environmentally friendly products is growing, and the production process of this compound does not conform to the concept of environmental protection, or it encounters obstacles in the promotion and sales. On the contrary, if it can conform to the current trend of environmental protection and high efficiency, it may stand out in the market and gain considerable profits and development space.