1h Pyrrole 3 Carboxamide N 2 Ethylamino Ethyl 5 Formyl 2 4 Dimethyl
pyridine pyrrole pyrazine piperidine piperazine

1H-Pyrrole-3-carboxamide,N-[2-(ethylamino)ethyl]-5-formyl-2,4-dimethyl-

    Specifications

    HS Code

    187402

    Chemical Formula C13H21N3O2
    Molecular Weight 251.325 g/mol
    Iupac Name N-(2-(Ethylamino)ethyl)-5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxamide
    Physical State Solid (assumed)
    Solubility Solubility characteristics would depend on solvent, likely somewhat soluble in polar organic solvents
    Vapor Pressure Low vapor pressure expected for a solid organic compound

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    Frequently Asked Questions

    As a leading 1H-Pyrrole-3-carboxamide,N-[2-(ethylamino)ethyl]-5-formyl-2,4-dimethyl- supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    1H-Pyrrole-3-carboxamide, what is the chemical structure of N- [2- (ethylamino) ethyl] -5-formyl-2,4-dimethyl-
    1H-pyrrole-3-formamide, N- [2- (ethylamino) ethyl] -5-formyl-2,4-dimethyl, the chemical structure of this compound is an important topic in organic chemistry. Looking at its name, it can be seen that it is based on a pyrrole ring. On the pyrrole ring, there is a formamide group at the 3rd position, and the nitrogen atom in this amide group is connected to [2- (ethylamino) ethyl], which is like a by-product of branches and leaves, and the structure is more complicated. And it is connected to a formyl group at the 5th position, which seems to add a special logo to the ring. Furthermore, the 2 and 4 positions each have methyl substitution, just like the two sides of the ring are decorated with specific groups.
    Its overall structure, the interaction of various groups, affects the whole body, making this compound have unique chemical properties and reactivity. The existence of formamide groups endows it with certain nucleophilicity and hydrogen bonding ability; the ethylaminoethyl chain segment may affect its solubility and steric resistance; formyl groups are often reactive activity check points and can participate in many organic reactions; and the introduction of dimethyl groups changes the electron cloud distribution and spatial shape of molecules. Such a structural design may have special uses and potential value in the fields of organic synthesis, drug research and development, etc. It is a chemical structure worthy of in-depth investigation.
    What are the physical properties of 1H-Pyrrole-3-carboxamide, N- [2- (ethylamino) ethyl] -5-formyl-2,4-dimethyl-
    1H-pyrrole-3-formamide, N- [2- (ethylamino) ethyl] -5-formyl-2,4-dimethyl This substance has the following physical properties:
    From the perspective, this substance may be in a specific crystalline form, the color may be pure white, or slightly yellowish, the crystal shape is regular, the luster is delicate, and it has a unique visual appearance. Touch it, the texture may be solid, but it is not as hard and brittle as gold stone, and its subtle texture can be felt when pinching.
    Smell it, its smell is specific, not pungent or unpleasant, nor is it fragrant. It is a subtle and unique smell, or it can trigger special memories of smell.
    As for its melting point, after rigorous experiments, the melting point is in a specific temperature range. At this temperature, the substance gradually melts from solid to liquid, and the process is smooth and orderly; the boiling point also has its fixed value. At this temperature, the liquid substance will be violently converted into gaseous state.
    In terms of solubility, in the solvent of water, the degree of solubility is limited, only slightly soluble, or a few particles are suspended and dispersed in it; however, in specific organic solvents, such as ethanol, acetone, etc., it can be well miscible and form a uniform and stable solution system. < Br >
    density is also one of its important physical properties. After accurate measurement, the mass per unit volume has its exact value, which is of key significance in related research and applications. All these physical properties are the basis for in-depth exploration of the chemical nature and application potential of this substance.
    What is the main use of 1H-Pyrrole-3-carboxamide, N- [2- (ethylamino) ethyl] -5-formyl-2,4-dimethyl-
    1H-pyrrole-3-formamide, N- [2- (ethylamino) ethyl] -5-formyl-2,4-dimethyl This substance is very important for modern uses. It may be a key raw material for the development of new drugs in the field of medicine. Due to its unique chemical structure, it may interact with specific targets in the human body and help in the treatment of diseases, such as fighting tumors and relieving inflammation.
    It may also have its uses in the field of materials science. Or it can be specially treated to have unique optical and electrical properties, so that it can be applied to the creation of new optoelectronic devices, such as organic Light Emitting Diodes, solar cells, etc., to promote the advancement of related fields.
    In addition to scientific research and exploration, it can be used as a model compound to help scientists explore the mechanism of organic chemical reactions, contribute to the development of organic synthetic chemistry, and expand the boundaries of human understanding of chemical transformation and properties. In short, this material has shown potential value in many fields, and it is a chemical substance that cannot be underestimated.
    What are the synthesis methods of 1H-Pyrrole-3-carboxamide, N- [2- (ethylamino) ethyl] -5-formyl-2,4-dimethyl-
    To prepare 1H-pyrrole-3-formamide, N- [2- (ethylamino) ethyl] -5-formyl-2,4-dimethyl, the following ancient method can be followed.
    First take the appropriate starting material, with the pyrrole derivative with dimethyl as the base. This derivative is placed in a suitable reaction vessel, dissolved in an organic solvent, and the raw material is uniformly dispersed. This organic solvent must be compatible with the subsequent reaction reagents and does not interfere with the reaction process.
    Then, a formylating agent is introduced, and under appropriate temperature and reaction conditions, it reacts with the pyrrole derivative to add 5-formyl group. This step requires precise temperature control, because too high or too low temperature can affect the efficiency and selectivity of formylation.
    After formylation is completed, another ethylamine reagent containing ethylamino is prepared, and the reaction system is slowly added. Adjust the pH and temperature conditions of the reaction environment, so that ethylamine reacts with specific positions on the pyrrole derivative to form the structure of N - [2 - (ethylamino) ethyl]. This substitution reaction also needs to be carefully regulated to prevent side reactions from occurring.
    During the reaction process, the reaction process is often monitored by thin-layer chromatography or other suitable analytical methods to observe the consumption of raw materials and the formation of products. When the reaction reaches the expected level, the target product is purified from the reaction mixture by conventional separation and purification methods, such as column chromatography, recrystallization, etc., to obtain a pure 1H-pyrrole-3-formamide, N- [2 - (ethylamino) ethyl] -5-formyl-2,4-dimethyl product. The whole process requires strict adherence to operating standards, precise temperature control, time control and reagent dosage control to obtain ideal results.
    1H-Pyrrole-3-carboxamide, N- [2- (ethylamino) ethyl] -5-formyl-2,4-dimethyl-what are the safety precautions
    1H-pyrrole-3-formamide, N- [2- (ethylamino) ethyl] - 5-formyl-2,4-dimethyl This substance is related to many safety precautions, and I will tell you in detail.
    This chemical may be toxic and must not be brought into contact with the skin. If you accidentally touch it, rinse it with plenty of water immediately and seek medical attention as soon as possible. Its volatile gas should not be inhaled. When operating, be sure to ensure that the space is well ventilated. It is best to perform relevant operations in the fume hood to prevent inhalation of harmful gases and damage to the body.
    Furthermore, when the substance encounters an open flame or hot topic, there is a risk of combustion and explosion. Therefore, the storage place should be kept away from fire and heat sources, and placed in a cool and dry place. It must not be mixed with reactive substances such as oxidants to avoid danger.
    During use, the utensils used must be clean and dry to prevent impurities from reacting with it and generating unknown harmful substances. Operators should also take protective measures, wearing protective clothing, protective gloves and goggles, etc., to ensure their own safety in all aspects.
    After the operation is completed, the remaining materials and waste must not be discarded at will, and must be properly disposed of in accordance with relevant regulations to prevent pollution to the environment and harm to all parties. Overall, this chemical must be treated with extreme caution and must not be taken lightly to ensure safety.