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What is the chemical structure of 4-ethyl-3-methyl-N- [2- [4- [ (4-methylcyclohexyl) carbamoylsulfamoyl] phenyl] ethyl] -5-oxo-2H-pyrrole-1-carboxamide?
This is a rather complex nomenclature for organic compounds. To clarify its chemical structure, it is necessary to gradually analyze it according to the nomenclature.
"4-ethyl-3-methyl-N - [2 - [4 - [ (4 - methylcyclohexyl) carbamoylsulfamoyl] phenyl] ethyl] - 5 - oxo - 2H - pyrrole - 1 - carboxamide". "4 - ethyl - 3 - methyl" is shown in the main structure, with ethyl and methyl groups connected at specific positions (4th and 3rd positions), respectively. " 2H - pyrrole - 1 - carboxamide "The main structure of the table is a pyrrole ring, and the 1 position is connected with a formamide group." 5 - oxo "indicates that the 5 position has a carbonyl group.
" N - [2- [4- [ (4 - methylcyclohexyl) carbamoylsulfamoyl] phenyl] ethyl] "This part is the substituent attached to the nitrogen atom. First "[2 - [4 - [ (4 - methylcyclohexyl) carbamoylsulfamoyl] phenyl] ethyl]", where "ethyl" is ethyl, which is connected to the benzene ring, and the 4-position of the benzene ring is connected to "[ (4 - methylcyclohexyl) carbamoylsulfamoyl]", that is, 4 - methylcyclohexyl is connected to the benzene ring through the carbamoyl group and the sulfamoyl group.
In summary, this compound takes the pyrrole ring as the core, and the ring is connected with a specific alkyl group, a carbonyl group and a formamido group. The formamido nitrogen atom is also connected with a substituent group containing complex structures such as benzene ring and cyclohexyl group. Its chemical structure is complex, and it is necessary to follow the naming rules carefully to clarify the connection and spatial arrangement of each atom and group.
What are the main uses of 4-ethyl-3-methyl-N- [2- [4- [ (4-methylcyclohexyl) carbamoylsulfamoyl] phenyl] ethyl] -5-oxo-2H-pyrrole-1-carboxamide?
This is an organic compound with a long and complicated name. Looking at the name of this compound, it may be used in the field of pharmaceutical research and development. In the exploration of modern medicine, it is often necessary to design and synthesize complex organic molecules. This compound may be a key intermediate for a new type of drug. After subsequent reaction transformation, it is expected to become a pharmaceutical entity with specific pharmacological activities.
Furthermore, it may be used in the field of materials science. With the advancement of science and technology, the demand for materials with special properties is increasing. Such complex structural organic compounds may endow materials with unique electrical, optical or mechanical properties, and then be applied to cutting-edge fields such as electronic devices and optical materials.
It may also play a role in the fine chemical industry. Fine chemicals focus on high added value and specific functions of products. This compound may be used as a special additive to improve product quality and performance, such as in coatings, inks, adhesives and other products, to enhance its stability, durability and other characteristics.
However, according to its name, it is difficult to determine its specific use. It is necessary to combine more background information and research information to clarify its exact application and potential value in various fields.
What are the physical properties of 4-ethyl-3-methyl-N- [2- [4- [ (4-methylcyclohexyl) carbamoylsulfamoyl] phenyl] ethyl] -5-oxo-2H-pyrrole-1-carboxamide?
This compound is named 4-ethyl-3-methyl-N - [2 - [4 - [ (4 - methylcyclohexyl) carbamoyl sulfonyl] phenyl] ethyl] -5 -oxo-2H -pyrrole-1 -formamide. Its physical properties are generally as follows:
In terms of appearance, this compound has a solid state shape and is often white or white-like powder. Due to the interaction between molecules, it forms a regular arrangement.
When it comes to melting point, due to the existence of many polar groups in the molecule, such as amide groups, they can form hydrogen bonds and strengthen intermolecular forces, so the melting point is quite high, roughly between 150 and 200 ° C.
In terms of solubility, because the molecule contains polar and non-polar parts, polar amide groups, etc. make it soluble in polar organic solvents, such as dimethyl sulfoxide (DMSO), N, N-dimethylformamide (DMF); while non-polar alkyl groups, cyclohexyl groups, etc., make it difficult to dissolve in non-polar solvents, such as n-hexane. In water, although there are polar groups that can interact with water, the overall molecule is large and the proportion of non-polar parts is not small, so the solubility is limited.
As for the density, due to the large number of atoms and tight arrangement in the molecular structure, the density is slightly higher than that of water, about 1.2-1.3 g/cm ³.
In addition, the compound contains a conjugated system and may absorb under specific wavelengths of ultraviolet light, which can be used for qualitative and quantitative analysis.
What is the synthesis method of 4-ethyl-3-methyl-N- [2- [4- [ (4-methylcyclohexyl) carbamoylsulfamoyl] phenyl] ethyl] -5-oxo-2H-pyrrole-1-carboxamide?
To prepare 4 - ethyl - 3 - methyl - N - [2 - [4 - [ (4 - methylcyclohexyl) carbamoylsulfamoyl] phenyl] ethyl] - 5 - oxo - 2H - pyrrole - 1 - carboxamide, the method is not the same, can follow the ancient way of organic synthesis, and follow various reactions.
At the beginning, appropriate starting materials can be taken first, such as pyrrole derivatives with specific substituents, phenethylamine derivatives and sulfonamides containing 4 - methylcyclohexyl groups. At the beginning of the reaction, the key fragments may be connected by double condensation reaction. For example, an acid chloride or anhydride is reacted with an amine group to perform an amidation reaction, and the carboxyl group on the pyrrole ring is connected to the amine group of the phenethylamine derivative to form an amide bond. This step may be required in a suitable solvent, such as dichloromethane, N, N-dimethylformamide, etc., accompanied by an alkali agent, such as triethylamine, pyridine, etc., to promote the progress of the reaction, so that the reaction system maintains a suitable pH, which is conducive to the formation of amide bonds.
Furthermore, in order to obtain the structure of 4 - [ (4 - methylcyclohexyl) carbamoylsulfamoyl], 4 - methylcyclohexylamine can be reacted with sulfonyl chloride, and the corresponding sulfonamide structure can be obtained through a series of steps such as aminolysis and condensation. In this process, the temperature, reaction time and other conditions need to be carefully controlled. If the temperature is too high, or side reactions may occur; if the time is too short, the reaction is not completed, and the product is impure.
Then, the two parts that have been generated are connected by organic synthesis methods, such as coupling reactions, etc., and the final product is obtained. Among this, the choice of catalyst is also crucial, such as the coupling reaction catalyzed by palladium, which can precisely connect different fragments. However, the amount of catalyst and the regulation of the reaction conditions need to be tried repeatedly to achieve the best synthesis effect, so that the yield and purity of the product are good. The process of synthesis requires caution, and every step is related to success or failure. Only by carefully observing the details of the reaction can the preparation of this compound be achieved.
What is the safety and toxicity of 4-ethyl-3-methyl-N- [2- [4- [ (4-methylcyclohexyl) carbamoylsulfamoyl] phenyl] ethyl] -5-oxo-2H-pyrrole-1-carboxamide?
This is a rather complex organic compound named 4-ethyl-3-methyl-N - [2 - [4 - [ (4-methylcyclohexyl) carbamoyl sulfonylamino] phenyl] ethyl] -5 -oxo-2H-pyrrole-1-formamide. However, it is difficult to directly judge its safety and toxicity based on its chemical name.
Generally speaking, the safety and toxicity of compounds need to be investigated through many rigorous experiments. At the laboratory level, cell experiments are often used to observe the effects of the compound on the growth, proliferation, morphology and function of various types of cells to preliminarily evaluate its potential toxicity. For example, if it can cause apoptosis, necrosis or metabolic disorders in cells, it suggests that it has certain toxicity.
Then, animal experiments are also a key link. Taking rodents such as mice and rats as objects, the compound is administered through different routes, such as oral administration and injection, to observe the animal's behavior, physiological indicators, and pathological changes of organs. If animals show weight loss, abnormal behavior, and organ damage, it can indicate that the compound is toxic.
In practical application scenarios, the exposure route and dosage need to be considered. If toxicity only appears under high concentrations and long-term exposure, and the human exposure dose is very low under normal use conditions, the actual safety may be relatively high. On the contrary, if it can have adverse effects on organisms at lower doses, and people are easily exposed to this compound in daily life, its safety is of concern.
Because we have not obtained specific experimental data and research data on this compound, it is difficult to determine its safety and toxicity with certainty. To accurately know its safety and toxicity characteristics, it is necessary to consult professional chemical and toxicological literature or conduct targeted experimental studies.