Methylthio 2 Pyridine French
pyridine pyrrole pyrazine piperidine piperazine

Methylthio-2 pyridine [French]

    Specifications

    HS Code

    320801

    Chemical Formula C6H7NS
    Molecular Weight 125.19
    Appearance Liquid
    Color Colorless to pale yellow
    Odor Pungent
    Boiling Point 204 - 206 °C
    Density 1.129 g/cm³
    Solubility In Water Slightly soluble
    Solubility In Organic Solvents Soluble in common organic solvents

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    General Information
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    Frequently Asked Questions

    As a leading Methylthio-2 pyridine [French] 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 Methylthio-2 pyridine [French]?
    Methylthio-2-pyridine (Methylthio-2-pyridine), the chemical structure of this substance can be known a little from its name. "Pyridine" is a nitrogen-containing six-membered heterocyclic compound with aromatic properties. The carbon atoms on its ring are numbered in sequence. The "2-position" refers to a specific position, where a "methyl thio" group is connected.
    "Methylthio", that is, the methyl group (-CH 🥰) is connected to the sulfur atom, which in turn is connected to the 2-position carbon atom of the pyridine ring. As a whole, the chemical structure of the compound is based on the pyridine ring as the core structure, and a substituent such as methyl thiogeneration (-SCH) is introduced at the 2-position. This structure endows the compound with unique physical and chemical properties, which can be used in many fields such as organic synthesis and medicinal chemistry, or have specific uses and reactivity. It can participate in various chemical reactions according to different needs and derive a variety of chemical products.
    What are the main uses of Methylthio-2 pyridine [French]?
    Methylthio-2-pyridine has a wide range of uses. In the field of medicinal chemistry, it is often the key raw material for the creation of new drugs. Due to its unique chemical structure, it can be reacted through delicate chemical reactions to construct structures that are compatible with bioactive molecules, thus providing a new way for the treatment of diseases. For example, in the development of antibacterial drugs, methylthio-2-pyridine is used as the starting material, and through multi-step reactions, compounds with high inhibitory activity against specific pathogens can be prepared. And because of its unique structure, it may avoid the problem of drug resistance of traditional antibacterial drugs.
    In the field of materials science, methylthio-2-pyridine also has extraordinary effects. When synthesizing special polymer materials, it can be introduced into the main chain or side chain of the polymer as a functional monomer. In this way, the synthesized material may have good electrical conductivity, optical activity or special adsorption properties. For example, it can be used to prepare optoelectronic materials, or to optimize the absorption and emission properties of materials to specific wavelengths of light, thereby improving the efficiency of optoelectronic devices.
    In organic synthesis chemistry, methyl thio-2 -pyridine is often used as a key intermediate. With its active reaction check point, it can react with many organic reagents such as nucleophilic substitution and electrophilic substitution, and then derive organic compounds with diverse structures. Through ingenious reaction design and conditioning, precise control of the structure and properties of the target product can be achieved, laying a solid foundation for the total synthesis of complex natural products and the creation of new organic functional molecules.
    What are the physical properties of methylthio-2 pyridine [French]?
    Methylthio-2-pyridine (Methylthio-2-pyridine), this substance is colorless to light yellow liquid, and it is clear and translucent. Its smell has a specific smell, but it is not pungent and intolerable. It has a unique smell, which seems to attract people to find out.
    In terms of its melting and boiling point, the melting point is very low. It is a liquid at room temperature, and the boiling point is moderate. It can be boiled into a gaseous state at a specific temperature range. Its density is slightly higher than that of water. If placed in water, it will slowly sink to the bottom of the water, just like a pearl falling into an abyss.
    In terms of solubility, this substance can be well miscible in organic solvents such as ethanol and ether, just like a fish entering water, free. However, the solubility in water is not good, and it can only be dissolved in a small amount, just like a lone boat on the vast river surface, and it is difficult to find a place to live.
    In terms of chemical stability, methyl thio-2-pyridine is quite stable under general conditions, just like a calm old man, and it is not alarmed. In case of strong oxidizers, strong acids and alkalis, etc., chemical reactions will also occur, structural changes, and properties will change, just like throwing boulders into a calm lake, setting off layers of waves.
    Its steam is heavier than air. If it leaks into the air, the steam will spread close to the ground, just like clouds and fog. It is necessary to pay attention to prevention to avoid potential safety hazards.
    What is the production method of Methylthio-2 pyridine [French]?
    The preparation method of methylthio-2-pyridine is not directly described in ancient books, but one or two can be deduced from the chemical theory.
    One method may be formed by chemical reaction between sulfur-containing reagents and pyridine derivatives. If a suitable thiol compound is used, under specific reaction conditions, it will react with 2-halopyridine. When a suitable base is used as a catalyst, in a suitable solvent, heated and stirred, the halogen atom and the sulfur atom of the thiol can undergo a substitution reaction to obtain methylthio-2-pyridine. The solvent for the reaction, or a polar aprotic solvent, such as N, N-dimethylformamide (DMF), can improve the solubility and reactivity of the reactants. Potassium carbonate can be selected as a base, which can promote the deprotonation of thiols, enhance their nucleophilicity, and make the substitution reaction easier.
    Another method can be obtained by methylation from pyridine-2-thiol. Select suitable methylation reagents, such as iodomethane, dimethyl sulfate, etc. In an alkaline environment, the sulfur anion of pyridine-2-mercaptan can undergo nucleophilic substitution with methylating reagents, and methyl groups are introduced into the sulfur atom to form methyl-2-pyridine. During the reaction, the control of alkaline conditions is crucial. If the basicity is too high or too low, it may affect the reaction rate and yield. If the basicity is too high, or side reactions occur; if the basicity is too low, the reaction is difficult to start.
    Furthermore, organic synthesis often requires multiple steps to reach the target product. Or the pyridine ring is modified first, and suitable substituents are introduced to make the subsequent reaction with sulfur groups more selective and efficient. In the synthesis process, separation and purification are also important links. Impurities can be removed by recrystallization, column chromatography, etc., to obtain pure methyl thio-2-pyridine. Although this specific thing is not detailed in ancient books, the principle of chemical synthesis, ancient and modern, can be prepared according to chemical principles and existing methods.
    Methylthio-2 pyridine [French] What are the precautions during use?
    Methylthio-2-pyridine This substance, when using, many matters need to be paid attention to.
    First, safety is paramount. This is a chemical substance, or toxic and irritating. When operating, be sure to wear protective equipment, such as protective clothing, gloves, goggles, and ensure that the working environment is well ventilated. If you accidentally touch the skin or eyes, rinse with plenty of water immediately, and seek medical treatment if necessary.
    Second, accurate access. Due to its special chemical properties, accurate dosage is essential. The dosage needs to be carefully planned before use, and the measurement process must be accurate, so as not to affect the reaction process or product quality. After taking it, properly seal and store it to avoid reaction with air, moisture, etc.
    Third, be familiar with the reaction. When this substance participates in the reaction, the unique reaction conditions, such as temperature, pH, reaction time, etc., all have a profound impact on the result. Study the relevant reaction mechanism and conditions in advance, and strictly control them during operation to obtain the expected results.
    Fourth, be cautious about compatibility. When mixed with other substances, it is necessary to clarify whether adverse reactions will occur. Some chemicals are mixed with each other, or cause violent reactions, endangering safety. Therefore, it is necessary to verify relevant information or conduct a small test before mixing.
    Fifth, waste is properly handled. After use, the remaining substances and waste must not be discarded at will. According to its chemical characteristics, follow environmental protection regulations and properly dispose of them to prevent environmental pollution. < Br >
    Only by paying high attention to the above things throughout the use can we ensure safety and achieve the purpose of use.