3 Methylthiophene 2 Carboxaldehyde
quinoline thiophene imidazole thiazole

3-Methylthiophene-2-carboxaldehyde

Taiy Chemical

    Specifications

    HS Code

    432290

    Name 3 - Methylthiophene - 2 - carboxaldehyde
    Chemical Formula C6H6OS
    Molar Mass 126.176 g/mol
    Appearance Liquid (expected, based on similar compounds)
    Solubility In Water Insoluble (predicted as it is an organic heterocyclic aldehyde)
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
    Odor Likely has a pungent or characteristic aldehyde - like odor
    Stability Stable under normal conditions but may react with oxidizing agents

    As an accredited 3-Methylthiophene-2-carboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing
    Storage
    Shipping
    Free Quote

    Competitive 3-Methylthiophene-2-carboxaldehyde prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615365036030 or mail to info@alchemist-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615365036030

    Email: info@alchemist-chem.com

    General Information
    Where to Buy 3-Methylthiophene-2-carboxaldehyde in China?
    As a trusted 3-Methylthiophene-2-carboxaldehyde manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
    Frequently Asked Questions

    As a leading 3-Methylthiophene-2-carboxaldehyde 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 physical properties of 3-Methylthiophene-2-carboxaldehyde?
    3-Methylthiophene-2-formaldehyde is a kind of organic compound. Its physical properties are quite important and play a key role in its performance in various chemical processes and practical applications.
    This compound is usually liquid at room temperature and pressure, with a certain volatility. Looking at its appearance, it is usually a colorless to light yellow transparent liquid, just like the clear oil, under light or a little luster, like a shining droplet.
    When it comes to boiling point, it is about a specific temperature range, which makes it transform from liquid to gas. The characteristics of boiling point are related to the operation process of distillation, separation, etc. When the mixed system containing this compound is heated and approaches the boiling point, it will vaporize first, so that it can be separated from other substances with different boiling points.
    In terms of melting point, it also has a specific value. When the temperature drops below the melting point, it will solidify from liquid to solid, and this process is like the morphological transformation of matter. The level of melting point is closely related to the intermolecular force. The characteristics of the intermolecular force of this compound determine that its melting point is in a certain range. This characteristic is of great significance in the storage and transportation of substances and the control of specific chemical reaction conditions.
    Its density is heavier than that of water. If it is mixed with water, it will sink to the bottom of the water, just like heavy objects sink, and the stratification phenomenon is significant. This property can be used as an important basis in operations involving liquid-liquid separation.
    In terms of solubility, it exhibits good solubility in organic solvents such as ethanol and ether, like fish entering water, but poor solubility in water. This property makes organic solvents a common reaction medium in organic synthesis reactions, so as to better dissolve the reactants and promote the smooth progress of the reaction.
    The physical properties of 3-methylthiophene-2-formaldehyde, from appearance, boiling point, melting point, density to solubility, have laid the foundation for its research and application in the field of chemistry, affecting the development of related operations and reactions.
    What are the chemical properties of 3-Methylthiophene-2-carboxaldehyde?
    3-Methylthiophene-2-formaldehyde, this is an organic compound, which has unique chemical properties and has important uses in many fields.
    Let's talk about its physical properties first. At room temperature, it is mostly liquid and has a special odor. Its boiling point, melting point and other properties depend on the intermolecular force. Due to the presence of thiophene rings and aldehyde groups in the molecule, the intermolecular force is unique, which determines its melting and boiling point. And it has good solubility in organic solvents, such as common ethanol, ether, etc., but poor solubility in water, because it is an organic molecule, and the force between water molecules is weak.
    Let's talk about chemical properties again. The presence of the aldehyde group gives it significant chemical activity. It can undergo oxidation reactions. In case of strong oxidants, the aldehyde group can be oxidized to a carboxyl group to obtain 3-methylthiophene-2-carboxylic acid. It can also undergo reduction reactions. Under the action of suitable reducing agents, the aldehyde group can be converted into hydroxyl groups to generate corresponding alcohols.
    In addition, it can also participate in nucleophilic addition reactions. In the carbon-oxygen double bond of the aldehyde group, the carbon atom has partial positive electricity and is vulnerable to attack by nucleophilic reagents. If it is catalyzed by acid with alcohols, acetals can be formed. This reaction is often used as a means of carbonyl protection in organic synthesis.
    thiophene ring also affects its chemical properties. The thiophene ring is aromatic and can undergo electrophilic substitution reaction. Due to the methyl group as the power supply, the electron cloud density of the thiophene ring will increase, and the localization effect makes the electrophilic substitution reaction more likely to occur at a specific location of the thiophene ring.
    In the field of organic synthesis, 3-methylthiophene-2-formaldehyde is an important intermediate. With its characteristics of aldehyde groups and thiophene rings, complex organic molecular structures can be constructed through various reactions, providing key raw materials for drug research and development, materials science, etc.
    What are the main uses of 3-Methylthiophene-2-carboxaldehyde?
    3-Methylthiophene-2-formaldehyde, which has a wide range of uses. In the field of organic synthesis, it is a key raw material. Due to its unique structure, it contains thiophene ring and aldehyde group, which give it active chemical properties. It can be used to construct various complex organic compounds through various chemical reactions, such as condensation reaction of aldehyde group, oxidation reaction, and electrophilic substitution reaction of thiophene ring.
    In the field of pharmaceutical chemistry, it is often used as a starting material to synthesize drug molecules with specific biological activities through a series of delicate reaction steps. In many drug research and development projects, its unique structure is relied on to lay the foundation for the creation of new drugs. < Br >
    In the field of materials science, it also has outstanding performance. It can be used as the cornerstone of building functional materials, and it can be introduced into polymer materials by chemical reactions, thereby giving materials such as special optical and electrical properties. For example, the preparation of organic optoelectronic materials shows potential application value in optoelectronic devices such as Light Emitting Diode, solar cells, etc.
    And because of its active chemical properties, in the field of fine chemicals, it is often used to synthesize high-value-added fine chemicals, such as fragrances, additives, etc., to add the unique properties and application range of products. In fact, it is a versatile and crucial organic compound.
    What are 3-Methylthiophene-2-carboxaldehyde synthesis methods?
    The synthesis method of 3-methylthiophene-2-formaldehyde has been known for a long time and is described in detail below.
    First, it can be started from 3-methylthiophene. First, it reacts with the corresponding reagent under specific conditions, introduces a carboxyl protecting group, and then converts the methyl group into an aldehyde group through an oxidation step. This process requires controlling the reaction temperature, time and amount of reagents. For example, a strong oxidant is slowly added dropwise in a low-temperature bath to monitor the reaction process in a timely manner to avoid excessive oxidation.
    Second, thiophene-2-formaldehyde is used as the raw material and the target product can be obtained through methylation. The key here is to choose the appropriate methylation reagent and catalyst. For example, an alkylation reagent, combined with a specific metal catalyst, is heated to a suitable temperature in an inert gas protective atmosphere to make the reaction proceed smoothly, and then 3-methylthiophene-2-formaldehyde is generated.
    Third, sulfur-containing heterocyclic compounds and aldehyde derivatives are also used as starting materials to construct target molecules through multi-step reactions. First, the two undergo a condensation reaction under alkali catalysis, and then go through steps such as reduction and rearrangement to obtain the final product. Each step of the reaction requires precise regulation of conditions to ensure the smooth progress of the reaction and improve the purity and yield of the product.
    These are all common synthesis methods of 3-methylthiophene-2-formaldehyde. The way of synthesis lies in fine, subtle knowledge and success.
    3-Methylthiophene-2-carboxaldehyde to pay attention to when storing and transporting
    3-Methylthiophene-2-formaldehyde is an organic compound. When storing and transporting, care must be taken to prevent accidental changes.
    When storing, the first choice is the environment. Find a cool, dry and well-ventilated place, away from fire and heat sources. Because of its flammability, it is easy to cause combustion in case of open flames and hot topics, so the source of fire must be eliminated. And the warehouse temperature should be strictly controlled, not too high, so as not to change the material properties.
    Furthermore, packaging is also crucial. Sealed packaging is required to prevent it from contacting with air. This compound may react with components such as oxygen in the air, causing quality damage. Packaging materials should also be considered, and should have good corrosion resistance and sealing properties to ensure the safe storage of substances.
    When transporting, the same should not be slack. Handling should be handled with care to avoid damage to the packaging container. If the packaging is damaged and the material leaks, it will not only cause losses, but also may cause danger due to contact with the external environment. Transportation vehicles should also ensure that they are clean and dry, and there are no other substances that may react with them. And during transportation, special personnel need to supervise, pay close attention to the state of the material, and dispose of it immediately in case of abnormal conditions.
    In addition, whether it is storage or transportation, relevant personnel need to be familiar with the properties, hazards and emergency treatment methods of 3-methylthiophene-2-formaldehyde. In the event of leakage and other accidents, it can respond quickly and correctly to minimize the harm. In this way, it is necessary to ensure the safety of 3-methylthiophene-2-formaldehyde during storage and transportation.