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4-[2-(2-Methoxy-5-Chlorobenzamido)Ethyl]Benzene Sulfonamide

Linshang Chemical

Specifications

HS Code

949696

Chemical Formula C16H17ClN2O4S
Molar Mass 368.839 g/mol

As an accredited 4-[2-(2-Methoxy-5-Chlorobenzamido)Ethyl]Benzene Sulfonamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage
Packing 500g of 4 - [2 - (2 - methoxy - 5 - chlorobenzamido)ethyl]benzene Sulfonamide in sealed bags.
Storage Store 4-[2-(2 - methoxy - 5 - chlorobenzamido)ethyl]benzene Sulfonamide in a cool, dry place. Keep it away from heat sources and direct sunlight, which could potentially degrade the chemical. Store in a tightly - sealed container to prevent moisture absorption and exposure to air, safeguarding its chemical integrity. Avoid storing near incompatible substances to prevent chemical reactions.
Shipping Ship 4-[2-(2 - methoxy - 5 - chlorobenzamido)ethyl]benzene Sulfonamide in sealed, corrosion - resistant containers. Ensure proper labeling for chemicals. Ship via approved freight carriers following all safety regulations for chemical transport.
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4-[2-(2-Methoxy-5-Chlorobenzamido)Ethyl]Benzene Sulfonamide 4-[2-(2-Methoxy-5-Chlorobenzamido)Ethyl]Benzene Sulfonamide
General Information
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Frequently Asked Questions

As a leading 4-[2-(2-Methoxy-5-Chlorobenzamido)Ethyl]Benzene Sulfonamide supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

What is the chemical structure of 4- [2- (2-methoxy-5-chlorobenzamido) ethyl] benzenesulfonamide?
To understand this chemical structure, it is necessary to clarify the groups and reactions involved. Groups such as ethyl and methoxy are mentioned here. The given formula "4 - [2 - (2 - methoxy - 5 - chlorophenylacetyl) ethyl] phenylacetic acid" can be analyzed step by step.
First look at the main structure, using phenylacetic acid as the basic structure. A substituent with a complex structure is attached at position 4 of the benzene ring. Looking from the outside to the inside, this substituent is first connected to an ethyl group at position 4 of the benzene ring. At one end of the ethyl group is connected to a larger structure, namely 2- (2-methoxy-5-chlorophenylacetyl).
Specifically, on a benzene ring, there is a methoxy group at position 2 and a chlorine atom at position 5. This benzene ring is connected to the aforementioned ethyl group through an acetyl group. In this way, the chemical structure of the compound is clearly presented. Its structure revolves around phenylacetic acid and is modified by substituents at different positions to form a unique chemical structure. Each group affects each other, giving the compound specific chemical properties and reactivity.
What are the main uses of 4- [2- (2-methoxy-5-chlorobenzamido) ethyl] benzenesulfonamide?
4- [2- (2-methoxy-5-bromobenzyloxy) ethyl] benzyloxybenzoic acid, this compound has significant uses in the field of medicinal chemistry. First, it can be used as an intermediate in organic synthesis to help build complex organic molecular structures. After a specific chemical reaction, it is combined with other reagents to form new compounds with specific functions, laying the foundation for the development of new drugs.
In the process of drug development, due to its unique chemical structure, it can be used to explore potential biological activities. By adjusting the molecular structure and changing the way it interacts with biological targets, lead compounds with therapeutic effects on specific diseases are screened, and the pace of new drug development is accelerated.
In the field of materials science, it may participate in the preparation of functional materials. Because it contains specific functional groups, it can endow materials with special properties, such as improving material solubility and stability, or giving materials the ability to recognize and respond to specific substances, and play a role in sensors, separation materials and other fields.
In addition, in the field of organic electronics, such compounds are expected to become key materials for building organic electronic devices. Using their electrical and optical properties, they can be used to fabricate organic Light Emitting Diodes, organic field effect transistors and other devices to promote the development of organic electronics.
What are the physical properties of 4- [2- (2-methoxy-5-chlorobenzamido) ethyl] benzenesulfonamide?
4 - [2 - (2 - methyl - 5 - bromobenzyloxy) ethyl] benzyloxybenzaldehyde, this is an organic compound. Its physical properties are diverse and closely related to the molecular structure.
First of all, the appearance properties, at room temperature and pressure, it is mostly white to pale yellow crystalline powder. This is due to intermolecular forces and crystal structures. The molecules are arranged in an orderly manner, resulting in a crystalline form of the substance, and the color is related to the intramolecular electron transition and conjugate system.
The melting point is of great significance in determining the purity and characteristics of the compound. The melting point is determined by experiments to be within a specific range. The melting point depends on the intermolecular forces, such as hydrogen bonds, van der Waals forces, etc. The stronger the intermolecular forces, the higher the energy required for melting, and the higher the melting point. The intermolecular forces of this compound determine its melting point characteristics. At a specific temperature, the thermal motion of the molecules intensifies enough to overcome the intermolecular forces, thus transforming from a solid state to a liquid state.
In terms of solubility, it has good solubility in organic solvents, such as common dichloromethane, chloroform, tetrahydrofuran, etc. This is attributed to the principle of "similar miscibility". The compound molecule has a certain hydrophobicity and can form a weak interaction with the organic solvent molecules, which promotes its dissolution. However, the solubility in water is poor. Due to the lack of strong interaction groups with water molecules in its molecular structure, the molecular force between water and the compound is weak, making it difficult to disperse it in water.
In addition, the density of the compound is also one of its physical properties. The density is closely related to the molecular mass and molecular accumulation. The molecular mass is large and the accumulation is close, and the density is relatively large. It has a specific density value under specific conditions, which is of great significance for the conversion of mass and volume in practical applications.
In practical operation and research, these physical properties provide a key basis for the separation, purification, identification and application of this compound. The purity can be determined by melting point determination; the appropriate solvent is selected for reaction, crystallization or extraction according to solubility; and the density data is helpful for accurately formulating the solution and designing the reaction system.
What are the synthesis methods of 4- [2- (2-methoxy-5-chlorobenzamido) ethyl] benzenesulfonamide?
To prepare 4 - [2 - (2 - methoxy - 5 - bromobenzyloxy) ethyl] benzyloxybenzoic acid, there are many ways to synthesize it.
First, you can take appropriate starting materials, such as aromatics containing methoxy and bromine atoms, and introduce halogen atoms precisely through halogenation reaction to determine the position of their substituents. Then make halogenated aromatics and compounds with hydroxyl groups under the catalysis of bases, carry out nucleophilic substitution reactions to obtain ether-linked intermediates. Then, by suitable oxidation steps, the specific group is converted into carboxyl groups, and the final target product is obtained.
Second, the structure of the benzyloxy group can also be constructed first, and suitable benzyloxy derivatives can be selected to react with halogenated hydrocarbons or sulfonates under suitable conditions to form benzyloxy groups. Subsequently, the obtained product is modified, such as the introduction of methoxy and bromine atoms. Or through Fu-gram reaction, etc., the corresponding substituent is added to the aromatic ring. After multi-step reaction, the required molecular skeleton is gradually constructed, and then oxidized to obtain the target carboxyl structure.
Third, a compound with a similar structure is used as the starting material and converted into a functional group. For example, the existing ester group is hydrolyzed into a carboxyl group; or the ether bond is broken and reconnected under specific conditions to adjust the molecular structure. The purpose of synthesizing 4- [2- (2-methoxy-5-bromobenzyloxy) ethyl] benzoxybenzoic acid can also be achieved through the transformation and modification of polyphanic functional groups.
All synthesis methods have their own advantages and disadvantages. In actual operation, many factors such as the availability of raw materials, the difficulty of reaction conditions, the yield and the impact on the environment need to be considered in order to choose the optimal synthesis path.
What are the precautions for using 4- [2- (2-methoxy-5-chlorobenzamido) ethyl] benzenesulfonamide?
4 - [2 - (2 - methyl - 5 - chlorobenzyl) ethyl] benzyl chlorobenzene should pay attention to the following matters during use:
First, this is a chemical substance, which is potentially dangerous, and safety procedures must be strictly followed during operation. Before starting the operation, be sure to know its physical and chemical properties, dangerous characteristics and other relevant information, such as its solubility, stability, flammability, toxicity, etc. Due to the lack of specific toxicological data, the operation should be assumed to be toxic, avoid skin contact, mouth and nose inhalation and accidental ingestion. During the operation, protective clothing, protective gloves and gas masks should be worn, and the contact area should be thoroughly cleaned after the operation.
Second, there is also attention to storage. It should be stored in a cool, dry and well-ventilated place, away from fire and heat sources, and protected from direct sunlight. Because it may react with certain substances, it should be stored separately from oxidants, acids, and alkalis. Do not mix storage to prevent dangerous reactions.
Third, the use environment should not be ignored. The operation should be carried out in a fume hood to ensure air circulation, discharge volatile steam in time, reduce the concentration of harmful substances in the air, and avoid the formation of explosive mixed gases. At the same time, the site should be equipped with corresponding fire equipment and leakage emergency treatment equipment, so as to respond quickly in case of emergencies.
Fourth, the use process should be strictly standardized. Precisely control the dosage and reaction conditions, and precisely adjust the concentration and dosage according to the experimental purpose or production requirements. Strictly control the reaction conditions such as temperature, pressure, reaction time, etc., to prevent accidents caused by runaway conditions. If the reaction is too violent, it will cause an explosion, or the formation of impurities will affect the quality of the product.
Fifth, waste treatment should not be underestimated. Residual substances, reaction products and waste packaging after use should not be discarded at will, and should be properly disposed of in accordance with relevant environmental protection regulations. Recyclable substances should be recycled; hazardous waste should be sent to a professional treatment institution for harmless disposal to prevent environmental pollution.