5 7 Dichloro 8 Hydroxy 2 Methylquinoline
quinoline thiophene imidazole thiazole

5,7-Dichloro-8-hydroxy-2-methylquinoline

Taiy Chemical

    Specifications

    HS Code

    206839

    Chemical Formula C10H7Cl2NO
    Molecular Weight 228.074 g/mol
    Appearance Solid (usually)
    Color May vary, often off - white or light - colored
    Odor Typically odorless or very faint odor
    Solubility In Water Low solubility in water
    Solubility In Organic Solvents Soluble in some organic solvents like ethanol, acetone
    Stability Stable under normal conditions if stored properly

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    General Information
    Where to Buy 5,7-Dichloro-8-hydroxy-2-methylquinoline in China?
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    Frequently Asked Questions

    As a leading 5,7-Dichloro-8-hydroxy-2-methylquinoline 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 chemical properties of 5,7-dichloro-8-hydroxy-2-methylquinoline?
    5% 2C7-dioxo-8-fluoro-2-methylbenzaldehyde, which is an organic compound. Its chemical properties are unique, with the typical characteristics of aldehyde groups, and many reactions can occur.
    The reduction of aldehyde groups is significant. When encountering weak oxidants such as Torun reagent (silver ammonia solution), a silver mirror reaction can occur. The aldehyde group is oxidized to a carboxyl group, and metal silver is formed at the same time, which adheres to the wall of the container. It is like a silver mirror. The reaction is exquisite and amazing; when encountering Feilin reagent, it can also reduce copper hydroxide to cuprous oxide, showing a brick-red precipitation. This reaction is often used for the identification of aldose. < Br >
    Because of its benzene ring structure, it also has the properties of aromatic hydrocarbon derivatives. The electron cloud density of the benzene ring is high, and it is prone to electrophilic substitution reactions. For example, under appropriate conditions, it can be substituted with halogens, nitric acid, sulfuric acid and other electrophilic reagents to generate corresponding halogens, nitro compounds and sulfonic acid compounds.
    Furthermore, the methyl group of its side chain and the substituents such as dioxy and fluoro will affect the electron cloud distribution of the benzene ring, thereby changing the reactivity and substitution position selectivity of the benzene ring. The interaction between the aldehyde group and its adjacent groups, or the electron storage effect and the space effect, exhibits different activities and selectivity in chemical reactions. These unique chemical properties enable them to occupy an important position in the fields of organic synthesis, medicinal chemistry, etc., and can be used as key intermediates for the synthesis of many complex and functional organic compounds.
    What are the common uses of 5,7-dichloro-8-hydroxy-2-methylquinoline?
    5% 2C7-dioxy-8-fluoryl-2-methacrylic acid, this substance is a very special chemical substance. In ancient times, although there was no such fine chemical understanding as modern times, if you explore its common uses from the perspective of that time, you can consider the following aspects.
    In the field of pill refining, ancient alchemists refined pills and often tried various strange substances. This compound contains fluorine, oxygen and other elements, and its unique chemical properties may attract the attention of alchemists. The activity of fluorine elements may be expected to be used to stimulate the special effects of pills, such as giving pills a unique "spiritual energy", so that those who take pills can strengthen their health and prolong their life. Although this idea lacks scientific basis in today's view, it can be regarded as a direction of exploration in the context of ancient alchemy.
    In terms of pigment modulation, ancient painters have never stopped pursuing pigments. The structure of this compound may show a unique color under certain conditions. If properly treated, it may become a special pigment for painting exquisite paintings, adding different colors and textures to the painting, helping the painter to paint a more realistic and colorful picture, which plays a role in the inheritance of painting art.
    As for metallurgical technology, ancient craftsmen in the metal smelting and processing, or found that the addition of this compound to certain metal smelting processes can change the characteristics of metals. Such as improving the hardness and toughness of metals, making them more suitable for making weapons, utensils, etc. Although it was difficult to clarify the chemical principles in ancient times, such phenomena were observed in practice and applied to the improvement of metallurgical technology.
    Although the ancient understanding was limited, the spirit of exploring various substances laid the foundation for the development of chemistry in later generations, leaving a unique historical trace in the exploration of the use of 5% 2C7-dioxy-8-fluoro-2-methacrylic acid.
    What is the synthesis method of 5,7-dichloro-8-hydroxy-2-methylquinoline?
    The synthesis of 5,7-dibromo-8-hydroxy-2-methylquinoline is a crucial research in the field of chemical synthesis. The synthesis steps are often complex and require many delicate operations and conditions to control.
    First, the molecular structure is gradually built by using specific starting materials and ingenious reaction paths. For example, starting with a compound containing quinoline parent nucleus, using brominating reagents to carefully adjust the reaction conditions, such as temperature, solvent, catalyst, etc., so that the bromination reaction occurs precisely at position 5,7. The key to this step is to ensure the selectivity and yield of bromination. The choice of brominating reagents is also very important, such as liquid bromine, N-bromosuccinimide (NBS), etc., and different reagents have different reactivity and selectivity.
    Then, for the introduction of the 8-position hydroxyl group, it is often necessary to use a suitable hydroxylation method. Or through a nucleophilic substitution reaction, a nucleophilic reagent containing hydroxyl groups is reacted with the corresponding intermediate; or through an oxidation reaction, a specific functional group is oxidized to obtain a hydroxyl group. In this process, the optimization of reaction conditions has a profound impact on the location and efficiency of hydroxylation.
    As for the introduction of 2-methyl, methylation reagents such as iodomethane and dimethyl sulfate can be used at an appropriate stage to achieve effective connection of methyl based on 2-position under alkali catalysis. In this step, attention should be paid to the dosage of methylation reagents, reaction time, and the type and dosage of bases to prevent excessive methylation or other side reactions.
    After each step of reaction, it is often necessary to separate and purify the product by means such as column chromatography and recrystallization to obtain high-purity 5,7-dibromo-8-hydroxy-2-methylquinoline. The entire synthesis process requires in-depth understanding and precise regulation of each step of the reaction in order to achieve efficient and high-quality synthesis.
    What are the precautions for storing and transporting 5,7-dichloro-8-hydroxy-2-methylquinoline?
    5,7-Dioxo-8-fluoro-2-methylbenzaldehyde is a special chemical substance. During storage and transportation, pay attention to the following things:
    First, when storing, it must be placed in a cool, dry and well-ventilated place. This is because the substance may be sensitive to heat and humidity. If it is exposed to high temperature and humidity, it may cause deterioration and damage its chemical properties and quality. As "Tiangong Kaiwu" said: "Everything has its own nature, and it will exist if it follows its nature, and it will die if it goes against its nature." This material likes dryness and coolness, and it will be harmful if it is not.
    Second, keep away from fire and heat sources. Because of its flammability, in case of open flames and hot topics, it is easy to cause combustion or even explosion. The ancients also knew the danger of fire and candles, so they must be careful where they are hidden. This chemical is even more so, and it should not be slack a little.
    Third, the storage container must be tightly sealed to prevent it from coming into contact with oxygen, moisture and other substances in the air and causing chemical reactions. Just like the ancients who hid wine, they must seal it with a pottery urn to keep it mellow. The same is true for this substance. A tight seal can protect its quality.
    Fourth, when transporting, make sure that the container is stable and will not be dumped or collided. Because if it is damaged and leaked during transportation, it will not only pollute the environment, but also pose a threat to personnel safety. In the past, when transporting fragile porcelain, it would also be handled with soft cushions and careful handling. In the transportation of this chemical substance, it should be imitated and fully protected.
    Fifth, transportation and storage should follow relevant laws and standards. Do not operate in violation of regulations, so as not to cause major disasters. Everything in the world has rules to follow, and if you follow them, it will be safe, and if you follow them, it will be chaotic. The storage and transportation of 5,7-dioxy-8-fluoryl-2-methylbenzaldehyde should also be carried out in accordance with regulations, so as to be worry-free.
    What are the effects of 5,7-dichloro-8-hydroxy-2-methylquinoline on the environment and human health?
    5% 2C7-dioxy-8-fluoryl-2-methacrylic acid has many effects on the environment and human health. If released in the environment, this compound can be toxic to aquatic organisms. In water bodies, it may interfere with the normal physiological activities of aquatic organisms, such as hindering their growth, development and reproduction. In severe cases, it can cause a large number of aquatic organisms to die and destroy the water ecological balance.
    In the soil environment, it may affect the structure and function of soil microbial community, interfere with material circulation and energy conversion in the soil, and then have an indirect impact on plant growth, resulting in poor plant growth and reduced yield.
    For human health, after entering the human body through respiration, skin contact or accidental ingestion, it may be irritating. If it comes into contact with the skin, it can cause redness, swelling, itching and even burning of the skin; when it comes into contact with the eyes, it can cause eye pain, tears and blurred vision.
    Inhalation of this substance, or irritation of the respiratory tract, causing symptoms such as cough, asthma, breathing difficulties, etc. Long-term exposure may be potentially carcinogenic and genotoxic, interfering with the normal cell metabolism and genetic information transmission of the human body, increasing the risk of cancer and the probability of genetic diseases. Therefore, when producing, using and handling substances containing this ingredient, it is necessary to take proper protective and handling measures to reduce the harm to the environment and human health.