2 Chloro 5 Thiophenecarboxaldehyde
quinoline thiophene imidazole thiazole

2-Chloro-5-thiophenecarboxaldehyde

Taiy Chemical

    Specifications

    HS Code

    863638

    Chemical Formula C5H3ClOS
    Molecular Weight 146.59
    Appearance A yellow - to - orange solid or liquid
    Boiling Point Approximately 108 - 110 °C at 10 mmHg
    Melting Point Around 33 - 35 °C
    Solubility Soluble in common organic solvents like dichloromethane, chloroform, and ethyl acetate
    Pungent Odor Yes
    Reactivity Reactive towards nucleophiles due to the presence of the aldehyde group and the electron - withdrawing chlorine on the thiophene ring

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    Frequently Asked Questions

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    What are the chemical properties of 2-Chloro-5-thiophenecarboxaldehyde?
    2-Chloro-5-thiophenylformaldehyde is one of the organic chemicals. It has unique chemical properties and is widely used in the field of organic synthesis.
    This compound contains chlorine atoms, thiophene rings and aldehyde groups. Chlorine atoms have certain electronegativity, which can affect the electron cloud distribution and reactivity of molecules. Because of its electronegativity, the electron cloud density of the carbon atoms connected to it can be reduced, making the carbon atoms more vulnerable to nucleophilic reagents attack, so it can participate in many nucleophilic substitution reactions, such as with alcohols under alkali catalysis, or nucleophilic substitution can occur to form ether derivatives.
    The thiophene ring is a five-membered heterocycle, which has aromatic properties and enhances molecular stability. At the same time, the electron cloud distribution is different from that of the benzene ring, and the activity and substitution position selectivity are also different in the electrophilic substitution reaction. The aldehyde group is an active functional group, and many typical reactions can occur. If it can condensate with ammonia and its derivatives to form Schiff base; it can also be oxidized to carboxylic acid, common oxidants such as potassium permanganate, potassium dichromate, etc. can be achieved; under the action of reducing agent, aldehyde group can be reduced to alcohol hydroxyl group. For example, using sodium borohydride or lithium aluminum hydride as reducing agent can reduce 2-chloro-5-thiophenaldehyde to the corresponding alcohol.
    In addition, the aldehyde group of 2-chloro-5-thiophene formaldehyde interacts with the adjacent thiophene ring and chlorine atoms, which enriches the chemical properties of the whole molecule. Due to the electron-absorbing effect of the aldehyde group, the electron cloud density on the thiophene ring decreases, which affects the electrophilic substitution reaction activity and position selectivity; and there is also an electronic effect interaction between the chlorine atom and the aldehyde group, which jointly determines the performance of the compound in various chemical reactions. In short, the chemical properties of 2-chloro-5-thiophene formaldehyde are determined by the functional groups contained and their interactions, and are of great significance in the fields of organic synthesis and medicinal chemistry.
    What are the common synthetic methods of 2-Chloro-5-thiophenecarboxaldehyde?
    The common synthesis methods of 2-chloro-5-thiophene formaldehyde are quite important in the field of organic synthesis. There are many synthesis paths, and the following are the common ones described in detail by Jun.
    One is to use thiophene as the starting material. First, thiophene is reacted through a specific reaction, and an aldehyde group is introduced at a specific position, and then a chlorine atom is introduced at a designated position. This process requires fine regulation of the reaction conditions, such as the reaction temperature, the proportion of reactants, and the catalyst used. In the aldehyde group introduction step, a specific acylating agent is often used, and under the catalysis of a suitable catalyst, the aldehyde group is introduced at a specific position of thiophene. The introduction of chlorine atoms requires the selection of suitable chlorination reagents and the appropriate reaction process to achieve the purpose of introducing chlorine atoms precisely at the predetermined position.
    Second, it can also be started from other compounds containing thiophene structures. Such compounds may already have some structural fragments of the target molecule, and the target product 2-chloro-5-thiophene formaldehyde is gradually constructed through a series of subsequent reactions, such as functional group conversion and substitution reactions. The key to this approach lies in the selection of the starting compound and the rational design and precise control of the subsequent reactions.
    Furthermore, the reaction strategy using transition metal catalysis is also a common method. Transition metal catalysts can effectively promote the reaction, improve the selectivity and yield of the reaction. For example, with the help of transition metal catalysts such as palladium and copper, the coupling reaction between halogenated aromatics and nucleophiles containing thiophene structures is realized, and then the carbon-carbon bond or carbon-hetero bond of the target molecule is constructed, and the synthesis of 2-chloro-5-thiophenylformaldehyde is gradually completed. In this process, factors such as the type of transition metal catalyst, the choice of ligand and the reaction solvent all play a crucial role in the effectiveness of the reaction.
    The common methods for synthesizing 2-chloro-5-thiophenylformaldehyde have their own advantages and disadvantages, and the most suitable synthetic route should be selected according to actual needs, such as the availability of raw materials, the cost of reaction, and the purity requirements of the target product.
    In what areas is 2-Chloro-5-thiophenecarboxaldehyde applied?
    2-Chloro-5-thiophenylformaldehyde is useful in many fields. In the field of medicinal chemistry, it is often a key intermediate for the synthesis of drugs. Because of its unique chemical structure, it can be combined with other compounds through various chemical reactions to produce a variety of drugs with specific pharmacological activities. For example, it can be used to develop antibacterial and antiviral drugs. By virtue of its structural properties, it can act on specific targets of pathogens, interfere with their physiological processes, and achieve the effect of treating diseases.
    In the field of materials science, there are also many examples. Can participate in the preparation of special functional materials, such as photoelectric materials. Due to its thiophene ring and aldehyde group, the material has special photoelectric properties, and can be used in organic Light Emitting Diode (OLED), solar cells and other devices to help the material absorb and convert light energy more efficiently and improve the performance of the device.
    In the field of organic synthetic chemistry, 2-chloro-5-thiophenylformaldehyde is an important cornerstone. Chemists can build complex organic molecular structures based on its structure through many reactions such as halogenation reaction, aldehyde group addition and oxidation reduction. Through ingenious reaction design and conditioning conditions, a series of organic compounds with unique structures and functions have been synthesized, contributing to the development of organic chemistry. < Br >
    In the fragrance and flavor industry, it may be used as a raw material for fragrance synthesis. With its own chemical properties, it generates compounds with unique aromas through specific reactions, adding different flavors to fragrance formulations, which are used to prepare perfumes, food flavors and other products to meet people's diverse needs for aroma.
    What are the physical properties of 2-Chloro-5-thiophenecarboxaldehyde?
    2-Chloro-5-thiophenylformaldehyde, this is an organic compound with specific physical properties. It is solid at room temperature, and it may appear white to light yellow crystalline. Its texture is delicate, like finely crushed jade, with a warm color.
    The melting point is about 60-64 ° C, just like ice melts when it is warm. When the temperature reaches this range, it gradually changes from solid to liquid, which is its important phase transition temperature. The boiling point is about 253-255 ° C. If it continues to heat up to this point, it will boil into a gaseous state, such as cloud evaporation.
    2-Chloro-5-thiophene formaldehyde is insoluble in water, like oil floating on the water surface in water, and the two are difficult to blend. However, it is soluble in many organic solvents, such as ethanol, ether, dichloromethane, etc., such as salt, which dissolves in water, and can be evenly dispersed in these solvents. Its solubility characteristics are closely related to its molecular structure. The chlorine atom, thiophene ring, and aldehyde group contained in the molecule cause it to interact weakly with water, but it can be combined with the organic solvent through specific intermolecular forces.
    In addition, its density is slightly larger than that of water, and when placed in water, it will slowly sink, like a stone falling in water, which is also one of its physical characteristics. And this thing has a certain smell, although it is difficult to describe accurately, it is unique and recognizable, just as each unique fragrance has its own special smell.
    What is the market price of 2-Chloro-5-thiophenecarboxaldehyde?
    2-Chloro-5-thiophene formaldehyde, an important intermediate in the field of organic synthesis, is widely used in many industries such as medicine, pesticides and materials. However, its market price is difficult to say in a word, because there are many factors affecting the audience.
    The first to bear the brunt is the market supply and demand relationship. If the demand for 2-chloro-5-thiophene formaldehyde is extremely strong at a certain time, but the supply is relatively short, its price will rise; on the contrary, if the market supply is sufficient, but the demand is small, the price will drop easily. For example, when the pharmaceutical industry develops a best-selling new drug with 2-chloro-5-thiophene formaldehyde as a key raw material, the demand for it will increase sharply, and the price will also rise.
    Furthermore, production costs are also a key factor. The price of raw materials, the complexity of the production process, energy consumption, etc. are all closely related to the cost. If the price of raw materials required to produce 2-chloro-5-thiophene formaldehyde rises, or the production process is complicated, a lot of manpower, material resources and technology need to be invested, and the cost will be high, which will lead to an increase in market prices.
    In addition, the price varies depending on the manufacturer. Well-known large factories, because of their high quality and good reputation, may have higher prices than some small factories. And large factories have large production scales, or can reduce costs by virtue of scale effects, but their brand added value and other factors will also affect the price.
    Regional factors should not be ignored. Different regions have different levels of economic development and market competition, and prices will fluctuate. Economically developed regions may have more reasonable prices due to diverse market demand and intense competition; while some remote areas may have higher prices due to high logistics costs and poor market liquidity. Therefore, in order to know the exact market price of 2-chloro-5-thiophene formaldehyde, it is necessary to pay attention to market trends in real time, comprehensively consider the above factors, or consult relevant chemical product suppliers and distributors to obtain more accurate price information.