2 Chloro 5 Pyridinesulfonyl Chloride
pyridine pyrrole pyrazine piperidine piperazine

2-Chloro-5-pyridinesulfonyl chloride

    Specifications

    HS Code

    903608

    Chemical Formula C5H3Cl2NO2S
    Molecular Weight 212.05
    Appearance Typically a solid
    Color May be colorless to pale yellow
    Odor Pungent odor
    Solubility Soluble in some organic solvents
    Melting Point Varies, but usually in a certain range
    Density Data depends on conditions
    Reactivity Reactive towards nucleophiles
    Hazard Class Corrosive, harmful

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    Frequently Asked Questions

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    What are the physical properties of 2-Chloro-5-pyridinesulfonyl chloride?
    2-Chloro-5-pyridine sulfonyl chloride is an important compound in organic chemistry. It has unique physical properties, which are described in detail by you today.
    This substance is mostly in the form of a solid state at room temperature, but it also changes slightly depending on the specific purity and environmental conditions. Looking at its appearance, it is usually a white to off-white crystalline powder, which is like a fine particle agglomeration, uniform and delicate.
    When it comes to melting point, it is about a certain range (although the exact value varies depending on the measurement method and conditions), usually in a relatively high temperature range, due to the intermolecular forces. When heated to the melting point, the substance gradually melts from the solid state to the liquid state, and this phase transition process is crucial for its subsequent processing and application.
    In terms of solubility, it exhibits different solubility characteristics in common organic solvents. In halogenated hydrocarbon solvents such as dichloromethane and chloroform, it has good solubility and can be uniformly dispersed to form a solution. This property is conducive to being used as a reactant or intermediate in organic synthesis reactions, enabling the reaction to proceed efficiently in a homogeneous system. In alcohol solvents, the solubility is relatively limited and can only be partially dissolved, which is due to the difference in molecular structure and the force between alcohol molecules. In water, 2-chloro-5-pyridyl sulfonyl chloride is almost insoluble. Due to the mismatch between the polarity of the molecule and the polarity of the water molecule, and the weak ability of the chlorine-containing and sulfonyl chloride groups to form hydrogen bonds with water, it is difficult to disperse in the aqueous phase.
    Its density is also an important physical property. Although the exact value needs to be accurately determined, it can be roughly inferred that it is a denser substance than water. This density characteristic is crucial when it comes to operations such as phase separation. In some reaction systems, its phase position can be determined based on this, so as to optimize the reaction process and separation process.
    In addition, 2-chloro-5-pyridine sulfonyl chloride has a certain volatility and will slowly emit an odor in the air. The odor is pungent and irritating. When used, it needs to be operated in a well-ventilated environment to prevent damage to the human respiratory tract.
    The above is the main physical properties of 2-chloro-5-pyridine sulfonyl chloride, which are related to each other and affect its application in many fields such as organic synthesis and chemical production.
    What are the chemical properties of 2-Chloro-5-pyridinesulfonyl chloride?
    2-Chloro-5-pyridine sulfonyl chloride is a key reagent in organic synthesis. Its chemical properties are unique and it has significant reactivity.
    First of all, the presence of chlorine atoms in this compound makes it electrophilic substitution activity. The chlorine atoms on the pyridine ring can participate in nucleophilic substitution reactions due to the characteristics of the electron cloud distribution of the pyridine ring. Nucleophilic reagents such as alcohols and amines can attack the carbon atoms attached to the chlorine atoms, causing the chlorine atoms to leave, and then form new carbon-oxygen, carbon-nitrogen and other chemical bonds.
    Furthermore, the sulfonyl chloride group (-SO 2O Cl) is also highly reactive. It can react violently with water to hydrolyze to form the corresponding sulfonic acid and hydrogen chloride. This hydrolysis reaction is very rapid and can be carried out spontaneously in a humid environment. And sulfonyl chloride groups can react with alcohols to form sulfonates. This reaction is often used in the preparation of sulfonates in organic synthesis. Sulfonates can be used as excellent leaving groups in many reactions to promote subsequent reactions.
    At the same time, 2-chloro-5-pyridine sulfonyl chloride can also react with amine compounds to form sulfonamides. Sulfonamides are widely used in the field of medicinal chemistry, and many drug molecules contain this group because of their unique biological activity and pharmacological properties.
    In addition, the electronic structure of the pyridine ring causes the whole molecule to exhibit unique electronic and spatial effects in some reactions, which affect the selectivity and rate of the reaction. In metal-catalyzed reactions, the pyridine ring can coordinate with the metal, changing the activity and selectivity of the metal catalyst, and then affecting the reaction path and product distribution of 2-chloro-5-pyridine sulfonyl chloride.
    What are the main uses of 2-Chloro-5-pyridinesulfonyl chloride?
    2-Chloro-5-pyridine sulfonyl chloride is a crucial chemical reagent in organic synthesis. It has a wide range of uses and is used in many fields such as medicine, pesticides and materials science.
    In the field of medicine, it is often a key intermediate for synthesizing drugs. Due to its unique chemical structure, it can combine with other molecules through chemical reactions to construct drug molecules with specific biological activities. For example, when developing new antibacterial drugs, 2-chloro-5-pyridine sulfonyl chloride can participate in the reaction, introducing key functional groups, giving the drug the ability to inhibit or kill specific bacteria.
    In the field of pesticides, it also plays an important role. It can be used to prepare highly efficient and low-toxicity pesticide products. By rationally designing the reaction path and reacting it with other organic compounds, the synthesized pesticide can accurately act on pests or weeds with little impact on the environment. For example, the synthesis of some new herbicides uses 2-chloro-5-pyridine sulfonyl chloride to build a unique chemical structure to enhance the herbicide effect on weeds, while reducing the harm to crops and surrounding ecosystems.
    In the field of materials science, 2-chloro-5-pyridine sulfonyl chloride can participate in the synthesis of functional materials. It can give materials special properties, such as improving the conductivity, optical properties or mechanical properties of materials. Taking the preparation of conductive polymers as an example, 2-chloro-5-pyridine sulfonyl chloride participates in the reaction, which helps to regulate the molecular structure of polymers, improve the electrical conductivity of materials, and make them suitable for electronic devices and other fields.
    In short, 2-chloro-5-pyridine sulfonyl chloride plays an indispensable role in the synthesis process of many fields due to its unique chemical properties, and is of great significance to promote the development of technologies in various fields.
    What are the synthetic methods of 2-Chloro-5-pyridinesulfonyl chloride?
    There are several common methods for the synthesis of Fu 2-chloro-5-pyridine sulfonyl chloride.
    First, pyridine is used as the starting material. First, pyridine is reacted with chlorosulfonic acid under specific conditions, and the hydrogen atom on the pyridine ring is replaced by a sulfonic acid group to obtain a pyridine sulfonic acid intermediate. This reaction requires temperature control, time control, and attention to the proportion of reactants. Then, the intermediate interacts with chlorinating agents such as phosphorus pentachloride or phosphorus oxychloride, and the sulfonic acid group is converted into a sulfonyl chloride group. In this process, the amount of chlorinating agent and the reaction environment are very critical. If it is not appropriate, side reactions will easily occur.
    Second, start from the corresponding pyridine derivatives. If suitable 2-substituted-5-pyridine derivatives are available, chlorine atoms and sulfonyl chloride groups can be introduced through specific steps. For example, chlorine atoms are introduced at specific positions with suitable halogenating reagents, and then sulfonyl chloride groups are constructed through sulfonation and chlorination steps. This approach requires fine design of the reaction sequence, and precise regulation of the reaction conditions at each step. For example, the choice of catalyst during halogenation, reaction temperature and time, etc., will affect the purity and yield of the product.
    Third, the reaction is catalyzed by transition metals. The target molecular structure is gradually constructed by coupling reactions with chlorine and sulfur-containing reagents in the presence of transition metal catalysts. Although this method is innovative, it requires strict reaction conditions. The selection and dosage of transition metal catalysts, the design of ligands, etc. are all related to the success or failure and efficiency of the reaction.
    All this synthesis method has its own advantages and disadvantages. In practical application, it is necessary to comprehensively consider factors such as raw material availability, cost, and product purity requirements.
    What to pay attention to when storing and transporting 2-Chloro-5-pyridinesulfonyl chloride
    2-Chloro-5-pyridine sulfonyl chloride is a chemical substance, and many matters must be paid attention to when storing and transporting it.
    Bearing the brunt, this substance is potentially harmful to the human body, touching the skin, eyes, or being inhaled or ingested can cause injury. Therefore, during storage and transportation, operators must wear protective clothing, goggles and gloves to avoid contact with it. The operating environment must also be well ventilated to avoid inhalation of its volatile gas.
    In addition, 2-chloro-5-pyridine sulfonyl chloride is active and easily reacts with water, alkalis, etc. When storing, a dry place must be selected, and it must be isolated from water and alkalis. The container should also be tightly sealed to prevent it from being damp or in contact with water vapor in the air, causing it to deteriorate.
    During transportation, also ensure that the packaging is intact to prevent it from leaking. If it unfortunately leaks, it should be disposed of immediately according to the corresponding emergency method. First adsorb with inert materials such as sand and vermiculite, and then collect it in a closed container and dispose of it properly according to regulations.
    In addition, temperature and light also affect its stability. It should be stored in a cool, dark place, protected from heat or direct light to prevent decomposition or other chemical reactions.
    In short, the storage and transportation of 2-chloro-5-pyridine sulfonyl chloride requires careful attention and strict adherence to relevant safety procedures to ensure the safety of personnel and the environment, and to avoid the occurrence of chemical accidents.