4 Chloropyridine 2 Carbaldehyde
pyridine pyrrole pyrazine piperidine piperazine

4-Chloropyridine-2-carbaldehyde

    Specifications

    HS Code

    151254

    Chemical Formula C6H4ClNO
    Molecular Weight 141.555 g/mol
    Appearance Yellow to orange solid or liquid
    Boiling Point 228 - 230 °C
    Melting Point 33 - 37 °C
    Density 1.324 g/cm³
    Flash Point 99 °C
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in many organic solvents like ethanol, acetone
    Pungent Odor Yes
    Cas Number 89488-29-9

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    General Information
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    Frequently Asked Questions

    As a leading 4-Chloropyridine-2-carbaldehyde 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 4-Chloropyridine-2-carbaldehyde?
    4-Chloropyridine-2-formaldehyde, an important chemical raw material in the field of organic synthesis, is widely used in medicine, pesticides, and materials science.
    In the field of medicine, it is often used as a key intermediate for the synthesis of drug molecules with specific biological activities. In many drug development processes, with the help of the unique chemical structure of 4-chloropyridine-2-formaldehyde, key functional groups can be introduced to construct compounds with precise pharmacological effects. For example, in the synthesis of some antibacterial and anti-inflammatory drugs, this compound will be used to shape effective drug ingredients combined with specific biological targets through a series of chemical reactions. < Br >
    In the field of pesticides, it also plays an important role. It can be used as an important starting material for the synthesis of new pesticides. Through chemical modification and transformation, pesticide products with efficient pest control and relatively friendly to the environment can be prepared. For example, for specific crop pests, insecticides developed based on 4-chloropyridine-2-formaldehyde can precisely act on the physiological system of pests, inhibit their growth and reproduction, and ensure the healthy growth of crops.
    In the field of materials science, 4-chloropyridine-2-formaldehyde can participate in the synthesis of functional materials. For example, in the preparation of some optoelectronic materials, their structural properties can be used to adjust the electronic transport properties and optical properties of the materials, thereby improving the application performance of the materials in optoelectronic devices such as organic Light Emitting Diodes (OLEDs), solar cells, etc., and promoting the device to exhibit better performance.
    In summary, 4-chloropyridine-2-formaldehyde occupies an indispensable position in many important fields due to its unique chemical structure and reactivity, and plays a key role in promoting the development of related industries.
    What are 4-Chloropyridine-2-carbaldehyde synthesis methods?
    The synthesis method of 4-chloropyridine-2-formaldehyde has been studied by many predecessors, and the current Chen number method is below.
    First, 4-chloropyridine is used as the starting material. First, it reacts with suitable reagents and introduces specific functional groups. For example, by using a strong base, 4-chloropyridine is deprotonated at a specific location, and then nucleophilic substitution is carried out with the corresponding halogenated aldehyde compound. This process requires precise control of reaction conditions, such as temperature, reaction time, and the proportion of reactants. If the temperature is too high or too low, it may cause more side reactions, affecting the yield and purity of the product. If the reaction time is too short, the reaction will be incomplete; if it is too long, it may cause the decomposition of the product or other side reactions.
    Second, start from pyridine-2-formaldehyde. First, the halogenation reaction of pyridine-2-formaldehyde is carried out. Appropriate halogenating reagents are selected, and chlorine atoms are introduced at the 4-position of the pyridine ring under appropriate reaction conditions. The choice of halogenating reagents is quite critical, and the activity and selectivity of different halogenating reagents vary. And the pH of the reaction system, the type of solvent and other factors also have an important impact on the reaction process and product distribution.
    Third, through the strategy of constructing pyridine rings. Using compounds containing appropriate substituents as raw materials, pyridine rings are formed by cyclization reaction, and chlorine atoms and aldehyde groups are introduced at the target position at the same time. This method requires clever design of the structure of the starting material and precise regulation of the cyclization conditions to ensure the formation of the target product.
    All these synthesis methods have advantages and disadvantages. It is necessary to carefully select the appropriate synthesis path according to actual needs, considering the availability of raw materials, cost, difficulty in controlling reaction conditions, and the purity and yield of the product, in order to achieve the best synthesis effect.
    What are the physical properties of 4-Chloropyridine-2-carbaldehyde?
    4-Chloropyridine-2-formaldehyde is an important compound in organic chemistry. It has many unique physical properties.
    Looking at its properties, 4-chloropyridine-2-formaldehyde is mostly in the state of light yellow to light brown crystalline powder at room temperature and pressure. This form is easy to store and use, and it is stable in general environments.
    When it comes to the melting point, the melting point of the compound is about 45-48 ° C. The characteristics of the melting point are of great significance for the identification and purification of the compound. Knowing the melting point, the purity can be judged by the method of melting point determination. If the melting point of the sample is consistent with the standard value and the melting range is narrow, it indicates that the purity is high; conversely, if the melting range is wide and the melting point deviates from the standard value, the purity is questionable.
    In terms of boiling point, the boiling point of 4-chloropyridine-2-formaldehyde is about 246.4 ° C. The boiling point is the temperature at which a substance changes from a liquid state to a gas state. This value shows that it can boil and vaporize at a higher temperature. This property is a key parameter in experiments such as distillation separation and industrial production operations. It determines the temperature conditions required for distillation and helps to separate it from other substances with different boiling points.
    Solubility is also an important property. 4-Chloropyridine-2-formaldehyde is slightly soluble in water, but soluble in common organic solvents, such as ethanol, dichloromethane, ether, etc. This difference in solubility provides a basis for the selection of solvents in organic synthesis reactions. When the aqueous phase reaction is difficult to carry out, a suitable organic solvent can be selected to make the reaction proceed smoothly.
    In addition, 4-chloropyridine-2-formaldehyde has a certain smell, although it is not strong and pungent, it also has a unique smell. This smell can be used as a basis for preliminary sensory judgment during operation, helping the operator to detect whether there is any abnormal situation such as leakage of the substance.
    What are the chemical properties of 4-Chloropyridine-2-carbaldehyde?
    4-Chloropyridine-2-formaldehyde is one of the organic compounds. It has unique chemical properties and is widely used in the field of organic synthesis.
    Looking at its chemical properties, the reactivity of aldehyde groups is first inferred. The aldehyde group is an active functional group and can participate in many chemical reactions. For example, it can react with alcohols through acetals to form acetals. This reaction is often used in organic synthesis to protect aldehyde groups or to build complex cyclic structures. During the reaction, the carbonyl group of the aldehyde group condenses with the hydroxyl group of the alcohol, removing a molecule of water to form acetals.
    Furthermore, the aldehyde group can be oxidized. When treated with appropriate oxidants, the aldehyde group of 4-chloropyridine-2-formaldehyde can be converted into a carboxyl group to obtain 4-chloropyridine-2-carboxylic acid. This process is often realized by mild oxidants such as manganese dioxide and Jones reagent, which is an important way to prepare pyridine carboxylic acids.
    And due to the presence of the pyridine ring, 4-chloropyridine-2-formaldehyde is basic. The nitrogen atom of the pyridine ring has lone pairs of electrons, can accept protons, and can form salts in acidic media. This alkalinity also affects the reactivity and solubility of the molecule.
    The chlorine atom is also a key functional group. It can participate in nucleophilic substitution reactions. When encountering nucleophiles, such as sodium alcohols, amines, etc., chlorine atoms can be replaced, introducing new functional groups, which greatly expands the possibility of compound derivation. The conditions of this nucleophilic substitution reaction vary depending on the activity of nucleophiles, and often need to be heated or carried out in the presence of appropriate catalysts.
    4-chloropyridine-2-formaldehyde has rich and diverse chemical properties, with aldehyde groups, pyridine rings and chlorine atoms showing their respective properties. It is an important cornerstone of organic synthetic chemistry and is of great value in many fields such as pharmaceutical chemistry and materials science.
    What is the price range of 4-Chloropyridine-2-carbaldehyde in the market?
    The price range of 4-chloropyridine-2-formaldehyde in the market is difficult to determine. Its price often changes due to many factors, such as the cost of raw materials, the difficulty of preparation, the supply and demand of the market, and even the difference between manufacturers.
    In the past, in the chemical market, the abundance of raw materials had a great impact on its price. If the raw materials required for the preparation of 4-chloropyridine-2-formaldehyde vary in output due to time of day, place of origin, etc., the price will fluctuate. If the preparation process is complicated, requires exquisite craftsmanship and many steps, and consumes more manpower and material resources, the price will also be high.
    Market supply and demand conditions also affect its price. If many manufacturers have a strong demand for 4-chloropyridine-2-formaldehyde at a certain time, but the supply is limited, the price will rise; on the contrary, if the supply exceeds the demand, the price will tend to fall.
    Produced by different manufacturers, the price is also different due to differences in quality and scale effect. If a large manufacturer has a scale advantage, the cost can be reduced, and the price may be more affordable; while if a small manufacturer focuses on quality and invests more, the price may be slightly higher.
    Roughly speaking, the price may range from a few yuan to tens of yuan per gram. However, this is only an approximate number, and the market conditions are ever-changing. To know the exact price, it is necessary to consult various chemical raw material suppliers or scrutinize the real-time quotations of chemical product trading platforms in order to obtain an accurate number.