5 Nitrothiophene 2 Carboxylic Acid
quinoline thiophene imidazole thiazole

5-nitrothiophene-2-carboxylic acid

Taiy Chemical

    Specifications

    HS Code

    217505

    Chemical Formula C5H3NO4S
    Molar Mass 173.147 g/mol
    Appearance Yellow solid
    Solubility In Water Insoluble
    Melting Point 185 - 189 °C
    Hazard Statement Harmful if swallowed, causes skin irritation, causes serious eye irritation

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    General Information
    Where to Buy 5-nitrothiophene-2-carboxylic acid in China?
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    Frequently Asked Questions

    As a leading 5-nitrothiophene-2-carboxylic 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 are the main uses of 5-nitrothiophene-2-carboxylic acid?
    5-Amino-imidazole-4-formamide (AIC), that is, 5-amino-4-formamidazole, is a crucial intermediate product in the synthesis of purine nucleotides. Its main uses are reflected in the following aspects:
    The primary use is to participate in the de novo synthesis path of purine nucleotides. In living organisms, the synthesis of purine nucleotides is a complicated and delicate process, and 5-aminimidazole-4-formamide, as a key part, goes through a series of complex enzymatic reactions, and finally interacts with other substances to gradually build the complete structure of purine nucleotides. This process plays a crucial supporting role in many important life activities such as cell growth, proliferation and transmission of genetic information. Without the participation of 5-aminoimidazole-4-formamide, the synthesis of purine nucleotides will be difficult to proceed smoothly, which will seriously affect the normal physiological functions of cells.
    Secondly, 5-aminoimidazole-4-formamide also plays a significant role in the regulation of energy metabolism. It can affect the energy perception and regulation mechanism in cells. Specifically, when the energy state of cells changes, 5-aminoimidazole-4-formamide and its related metabolites can act as signaling molecules to activate or inhibit specific signaling pathways, prompting cells to adjust their energy metabolism accordingly. For example, when cells are short of energy, it can participate in initiating a series of adaptive responses, helping cells to use existing energy substances more efficiently to maintain normal physiological activities of cells.
    Furthermore, in some studies, 5-aminoimidazole-4-formamide has been found to be associated with the occurrence and development of certain diseases. On the one hand, its metabolic abnormalities may lead to disorders of purine metabolism, which in turn lead to related diseases such as gout. On the other hand, in the metabolic process of tumor cells, the purine synthesis pathway involved in 5-aminoimidazole-4-formamide is often very active, which provides a necessary material basis for the rapid proliferation of tumor cells. Based on this, the study of 5-aminoimidazole-4-formamide-related metabolic pathways is expected to provide new targets and strategies for the treatment of tumors and other diseases.
    What are the physical properties of 5-nitrothiophene-2-carboxylic acid?
    5-Carboxycytidine-2-deoxyribonucleic acid, that is, 5-Carboxy-2-deoxycytidine, is a class of nucleic acid derivatives. Its physical properties are quite unique, as detailed below:
    - ** Properties **: Under normal conditions, it is mostly white to off-white powdery substances, with fine texture and pure appearance. This morphology is conducive to its uniform dispersion in various biochemical reaction systems, and then fully participate in the reaction.
    - ** Solubility **: Shows good solubility in water, capable of forming a stable interaction with water molecules, rapidly dissolving to form a uniform solution. This property allows it to conveniently participate in various biochemical reactions in the aqueous environment. In the physiological environment of the cell, it can smoothly transport with the cell fluid and participate in important life activities such as nucleic acid synthesis and metabolism. However, in common organic solvents such as ethanol and ether, its solubility is poor, which limits its application in systems that use these organic solvents as reaction mediums.
    - ** Stability **: In conventional temperature and humidity environments, it has certain stability. However, if the ambient temperature is too high, the chemical bond vibration in the molecule will intensify, which may cause structural changes and reduce stability; when the humidity is too high, water molecules may participate in the process of changing their molecular structure and affect their chemical properties. In addition, light, especially ultraviolet radiation, may trigger photochemical reactions and destroy its molecular structure, so it needs to be properly stored under low temperature, dry and dark conditions to maintain the stability of its structure and properties.
    - ** Melting point **: Has a specific melting point, when the temperature rises to a certain exact value, the substance will change from solid to liquid. This melting point value is crucial for identifying this substance and controlling its application in high temperature environments. By measuring the melting point, it can assist in judging the purity and structural integrity of the substance.
    What are the synthesis methods of 5-nitrothiophene-2-carboxylic acid?
    The synthesis method of 5-aminoimidazole-2-formamide has been known for a long time, and is now described in Chinese.
    First, the corresponding halogenate is used as the starting material. Take halogenated imidazole derivatives and reagents containing aminoformyl groups in suitable solvents, such as alcohols, ethers or aromatic hydrocarbon solvents, and use bases as catalysts, such as potassium carbonate, sodium carbonate or organic bases, etc., to control the temperature and slowly react. During this process, halogen atoms and aminoformyl groups undergo a substitution reaction to form 5-aminoimidazole-2-formamide. The principle lies in the activity of halogen atoms, which is easily replaced by nucleophiles, and the existence of bases can promote the progress of the reaction, adjust the pH of the reaction system, and move the reaction in the direction of generating the target product.
    Second, it is formed by cyclization reaction. Select compounds containing nitrogen and carbonyl groups, and under specific conditions, make them cyclize in the molecule. For example, with suitable amides and nitriles, under the catalysis of strong acids or strong bases, in a high temperature environment, the groups in the molecule are rearranged and cyclized to construct an imidazole ring structure, and then 5-aminimidazole-2-formamide is formed. This method focuses on the rearrangement and cyclization of intramolecular chemical bonds, and cleverly uses the structural characteristics of the compound itself to achieve the synthesis of the target product through the regulation of external conditions. The control of reaction conditions is extremely critical. The type and concentration of strong acid or strong base, and the specific degree of high temperature will affect the rate of reaction and the purity of the product.
    Third, biosynthesis is also involved. Using the catalytic properties of microorganisms or enzymes to synthesize by specific metabolic pathways. During the growth and metabolism process of some microorganisms, simple carbon sources, nitrogen sources and other substances can be gradually synthesized 5-aminoimidazole-2-formamide through complex enzymatic reactions in the body. This method has the advantages of green, high efficiency, and strong selectivity, but it requires strict environmental requirements for the reaction, requires precise control of microbial growth conditions, such as temperature, pH, nutrient concentration, etc., and the screening and cultivation of microorganisms also requires a lot of effort.
    What fields are 5-nitrothiophene-2-carboxylic acids used in?
    5-Serotonin-2 receptor antagonists are used in medicine, neuroscience and other fields. The details are as follows:
    - ** Medical field **:
    - ** Psychiatric treatment **: At the antidepressant level, it can regulate neurotransmitters and relieve depression symptoms. For example, some new antidepressants, by blocking the 5-serotonin-2 receptor, correct the abnormal function of the 5-serotonin system and improve the patient's mood. In antianxiety treatment, it can relieve symptoms such as nervousness and anxiety in patients and help them return to normal life. < Br > - ** Antiemetic Application **: It acts on the central related receptors of brain vomiting, effectively preventing and treating nausea and vomiting caused by chemotherapy and radiotherapy. For example, during chemotherapy, patients often vomit due to side effects of drugs, and such antagonists can significantly reduce the symptoms and improve the quality of life of patients.
    - ** Neuroscience Research **:
    - ** Neural Mechanism Exploration **: As a tool drug, it helps researchers to clarify the mechanism of action of serotonin nervous system in learning, memory, emotion regulation and other neural activities. By using antagonists on animals to observe their behavior and neural activity changes, in-depth study of neural pathways and functions.
    - ** Brain Disease Research **: For migraine, because the serotonin nervous system is closely related to the pathogenesis of migraine, antagonists can relieve vasodilation and neurogenic inflammation, providing direction for the treatment of migraine. For neurodegenerative diseases such as Alzheimer's disease, it helps to explore the mechanism of neurotransmitter imbalance in the disease and seek potential therapeutic targets.
    What is the market prospect of 5-nitrothiophene-2-carboxylic acid?
    In today's world, 5-hydroxytryptophan and tryptophan are in the market, and their situation is worth studying carefully.
    5-hydroxytryptophan is an intermediate product of tryptophan metabolism. It has also attracted much attention in the market. Gai because it can be involved in the synthesis of serotonin, which is involved in many physiological and psychological functions such as mood, sleep, and appetite. Therefore, health seekers, those who seek to improve sleep or soothe their emotions, should always pay attention to it. However, in the market, there is also a need for regulation. Although it has potential benefits, excessive or improper use may lead to side effects such as gastrointestinal discomfort, nausea, and dizziness. When it is sold on the market, it should be carried out according to the regulations, and it should be detailed in the logo, dosage, and applicable population, so that the public can understand its advantages and disadvantages, and use it with caution.
    Tryptophan, one of the essential amino acids of the human body. In the city, there is also a place. It is a raw material for the synthesis of serotonin, which can help sleep and adjust mood. It is commonly found in the food supplement market, such as health products. However, its market situation is also negotiable. The quality of products in the market varies, and quality supervision must be strict. Some merchants may exaggerate its effect and mislead consumers. And tryptophan intake should also be moderate, and too much is harmful to the body. Therefore, in the market, it is necessary to establish clear regulations to ensure quality, so that consumers know its nature and use it safely.
    To sum up, 5-hydroxytryptophan and tryptophan are in the market, and opportunities and challenges coexist. If you want to make profits, you must strictly regulate the market, clarify its utility and risk, so that consumers can benefit from it, and the market must develop in an orderly manner.