2 Methyl 3 Tetrahydrothiophene
quinoline thiophene imidazole thiazole

2-Methyl-3-tetrahydrothiophene

Taiy Chemical

    Specifications

    HS Code

    666657

    Name 2-Methyl-3-tetrahydrothiophene
    Chemical Formula C5H10S
    Molar Mass 102.198 g/mol
    Appearance Colorless to light yellow liquid
    Odor Characteristic sulfur - like odor
    Density ~0.99 g/cm³
    Boiling Point 135 - 137 °C
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in common organic solvents
    Flash Point Approximately 27 °C
    Vapor Pressure At 20°C, relatively low but measurable

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    General Information
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    Frequently Asked Questions

    As a leading 2-Methyl-3-tetrahydrothiophene 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 2-Methyl-3-tetrahydrothiophene?
    2-Methyl-3-tetrahydrothiophene is one of the organic compounds. It has a wide range of uses and has important applications in many fields.
    In the fragrance industry, 2-methyl-3-tetrahydrothiophene has unique aroma characteristics and can be used as a fragrance component. Because it can give products a special smell, it is often used in the preparation of various flavors, such as food flavors, daily chemical flavors, etc. In food flavors, it can add unique flavor and make food more attractive; in daily chemicals such as perfumes, air fresheners, etc., it can create a unique fragrance atmosphere.
    In the field of pharmaceutical chemistry, it is an important organic synthesis intermediate. Chemists can modify and transform their structures to synthesize a variety of biologically active compounds for the development of new drugs. The special structure of this compound provides a unique framework for the design of drug molecules, or can endow drugs with specific pharmacological activities and pharmacokinetic properties.
    Furthermore, in the field of materials science, 2-methyl-3-tetrahydrothiophene may participate in the synthesis of some functional materials. For example, it can be used as a monomer to build a specific polymer structure, endowing materials with special electrical, optical or mechanical properties, providing new avenues and possibilities for the development of new materials. Therefore, although 2-methyl-3-tetrahydrothiophene is an organic small molecule, it plays an indispensable role in many fields such as fragrances, medicine and materials, and is of great significance to the development of related industries.
    What are the physical properties of 2-Methyl-3-tetrahydrothiophene?
    2-Methyl-3-tetrahydrothiophene is one of the organic compounds. Its physical properties are quite specific, and are described in detail as follows:
    First of all, its appearance, under room temperature and pressure, is mostly colorless to light yellow transparent liquid, clear in appearance, luster flowing, like jade liquid. This state is convenient for it to participate in many chemical reactions and industrial processes. Because of its good fluidity, it is easy to mix and transfer.
    As for the smell, it has a special sulfur ether smell, unique and bright, and the smell is impressive. Although this odor is not as pleasant as a floral fragrance, it is an important characteristic in the field of chemistry to identify its existence. Chemical engineers often use this odor to determine whether this substance is present in the system.
    Its boiling point is also a key physical property. Boiling in a specific temperature range, this temperature value is of great significance in the separation and purification process. With precise temperature control and the use of its boiling point characteristics, it can be effectively separated from the mixture to obtain a pure product.
    Furthermore, the melting point cannot be ignored. Under the corresponding low temperature conditions, this material will change from liquid to solid. This transition temperature point provides a key reference for storage and transportation, ensuring that it maintains the required physical form under a suitable temperature environment, and will not affect the quality and use due to improper temperature.
    In terms of density, there is a specific value, which is lighter or heavier than water and other common solvents. This property is related to its distribution in the mixed system. It is closely watched by chemical practitioners in phase separation, extraction and other operations.
    Solubility is also an important characteristic. In organic solvents such as alcohols and ethers, it exhibits good solubility and can dissolve with them to form a uniform and stable solution. This property greatly expands its application in organic synthesis reactions, provides a suitable environment for reactions, and helps various chemical reactions proceed smoothly.
    2-methyl-3-tetrahydrothiophene has rich and diverse physical properties, and each property is interrelated. It plays an indispensable role in chemical research, industrial production and many other fields, laying a solid foundation for the development of related work.
    What is the chemistry of 2-Methyl-3-tetrahydrothiophene?
    2-Methyl-3-tetrahydrothiophene is a kind of organic compound. This substance has unique chemical properties and is often used as a key intermediate in the field of organic synthesis. It has a wide range of uses in perfumes, medicines and pesticides.
    In terms of its chemical properties, the molecular structure contains thiophene rings and methyl groups, which cause it to exhibit specific reactivity. Thiophene rings are electron-rich aromatic heterocycles and have aromatic properties. They can undergo many aromatic electrophilic substitution reactions, such as halogenation, nitrification, sulfonation, etc. For example, under appropriate conditions, they can react with halogens to introduce halogen atoms on thiophene rings. This halogenated product is an important raw material for the subsequent synthesis of more complex compounds.
    The connection of methyl to a specific position of the thiophene ring affects the distribution and spatial structure of the molecular electron cloud, which in turn affects the reaction selectivity. In the electrophilic substitution reaction, methyl as the power supply group will increase the electron cloud density of the adjacent and para-position of the thiophene ring, making it easier for the electrophilic reagents to attack the adjacent and para-position, showing specific regioselectivity.
    The sulfur atom of 2-methyl-3-tetrahydrothiophene also gives it special chemical properties. The sulfur atom has lone pairs of electrons and can be used as an electron donor to participate in the reaction, forming coordination bonds with metal ions, which may play an important role in some organometallic catalytic reactions. At the same time, sulfur atom-related reactions, such as oxidation reactions, can convert them into sulfoxides or sulfone compounds, expanding their applications in organic synthesis.
    In addition, 2-methyl-3-tetrahydrothiophene has certain flammability due to the presence of carbon, hydrogen, sulfur and other elements. When storing and using, it is necessary to pay attention to the safety issues caused by its flammability, follow relevant safety regulations, and ensure the safety of the operating environment.
    In short, 2-methyl-3-tetrahydrothiophene has diverse chemical properties due to its unique structure, which is of great significance in organic synthesis and other fields. However, its reaction characteristics and safety issues should be taken into account when using it.
    What are 2-Methyl-3-tetrahydrothiophene synthesis methods?
    The synthesis method of 2-methyl-3-tetrahydrothiophene has been known for a long time, and now it is detailed for you.
    First, it can be formed by condensation reaction of compounds containing sulfur and corresponding carbon chains. If an appropriate halogenated hydrocarbon and a sulfur-containing nucleophile are used, under suitable solvent and alkali catalysis conditions, the two interact, and the halogen atom is replaced by a sulfur atom, thereby constructing the basic skeleton of tetrahydrothiophene. And if the halogenated hydrocarbon has a methyl substituent, this structure can be retained during the reaction, and the final product is 2-methyl-3-tetrahydrothiophene. The reaction solvent is commonly selected as a polar aprotic solvent, such as dimethylformamide, which can promote the activity of nucleophiles and accelerate the reaction process. Potassium carbonate is mostly used as a base, which can provide an alkaline environment and promote the positive progress of the reaction.
    Second, it is prepared by cyclization reaction. Sulfide compounds containing unsaturated bonds and appropriate substituents are selected, and under the action of a specific catalyst, intramolecular cyclization occurs. In this process, the unsaturated bonds are opened and connected to the sulfur atom to form a tetrahydrothiophene ring, while retaining the corresponding position of methyl. The catalysts used, or metal salts, such as some transition metal salts, can effectively reduce the activation energy of the reaction and improve the selectivity and rate of the reaction. The reaction conditions need to be precisely controlled, and the temperature and pressure are all exquisite. Generally speaking, moderate heating can speed up the reaction rate, but too high temperature may lead to more side reactions.
    Third, natural products are used as the starting material and obtained through a series of chemical modifications. Some sulfur-containing compounds in nature have a similar structure to 2-methyl-3-tetrahydrothiophene, and are gradually converted into the target product through appropriate oxidation, reduction, substitution and other reactions. The advantage of this approach is that the starting material source is natural and green, but the reaction steps are often cumbersome, requiring fine separation and purification operations to obtain high-purity products.
    All these methods of synthesis have their own advantages and disadvantages, and they need to be considered comprehensively according to factors such as actual demand, availability of raw materials, and cost, and carefully selected to achieve the purpose of synthesis.
    2-Methyl-3-tetrahydrothiophene what are the precautions during use
    2-Methyl-3-tetrahydrothiophene is an organic compound. During use, many matters need to be carefully paid attention to. The details are as follows:
    First, it is related to safety. This compound is flammable. In the place of use, open flames and hot topics must be strictly avoided to prevent the risk of fire and explosion. At the same time, its volatile vapor may form an explosive mixture with the air, so the work site must be well ventilated to disperse the accumulated vapor. In addition, it may be irritating to the eyes, respiratory tract and skin. During operation, protective equipment such as goggles, masks, gloves, etc. are indispensable. Once inadvertently touched, rinse with plenty of water immediately and seek medical attention in time according to the injury.
    Second, about storage. It should be stored in a cool and ventilated warehouse, away from fire and heat sources. The temperature of the warehouse should be controlled within a suitable range to prevent its volatilization from being exacerbated or other hazards caused by excessive temperature. It should be stored separately from oxidizing agents, and should not be mixed with them, because they may react violently with certain substances. And the storage area should be equipped with suitable materials to contain leaks.
    Third, it involves operating specifications. The operation process strives to be airtight and ventilated. Operators must be specially trained and strictly abide by the operating procedures. When taking it, pay attention to accurate measurement to avoid waste and excessive use. After use, properly clean up the use site and appliances to prevent subsequent problems caused by residual substances. In addition, the waste generated during use must be properly disposed of in accordance with relevant regulations and cannot be discarded at will to avoid polluting the environment.