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What is the chemical structure of N, n '-bis (2,3-dihydroxypropyl) -5- [ (hydroxyacetyl) (2-hydroxyethyl) amino] -2,4,6-triiodobenzene-1,3-dicarboxamide?
Alas! This is a high-grade chemical name, and its chemical name is. This name "N, N '- (2,3-dipropyl) -5 - [ (acetyl) (2-ethyl) amino] -2,4,6-triiodobenzene-1,3-diformamide".
First, its main benzene group, above monobenzene, is a formamide group at positions 1 and 3, and this benzene-bis substituent, the characteristic of the amide group plays an important role in this group. At the 5th position, a phase is connected to the amino group, [ (acetyl) (2-ethyl) amino], which is composed of the acetyl group and 2-ethyl group together on the amino group, adding to the water content and versatility of the molecule.
And the 2,4,6 positions of benzene, each of which is an iodine atom. The introduction of iodine atoms will affect the properties of the molecule, such as density and refractive index. Furthermore, N, N '- (2,3-dipropyl), that is to say, the nitrogen atom is connected to a 2,3-dipropyl group, and the dipropyl group has more dipropyl groups, which greatly enhances the water quality of the molecule, and the dipropyl group may form dipropyl, which also has a great effect on the molecular image and properties.
Of course, this reduction is due to the combination of multiple special groups, which has special physical and chemical properties, and may have important uses in the chemical field.
What are the main uses of N, n '-bis (2,3-dihydroxypropyl) -5- [ (hydroxyacetyl) (2-hydroxyethyl) amino] -2,4,6-triiodobenzene-1,3-dicarboxamide?
N, N '-bis (2,3-dihydroxypropyl) -5- [ (hydroxyacetyl) (2-hydroxyethyl) amino] -2,4,6-triiodobenzene-1,3-diformamide is a chemical substance. It has a wide range of uses and is often used as a contrast agent in the field of medical imaging. Because of its structure containing iodine atoms, it has a high electron density. After being injected into the human body, it can effectively change the X-ray absorption characteristics of tissues and help doctors clearly observe the morphology and function of organs and blood vessels. It plays a key role in examinations such as cardiovascular angiography, urography, and CT enhanced scanning.
And in the process of drug development, this compound may be used as a lead compound to provide the basis for the creation of new contrast agents or drugs with specific physiological activities. Researchers can use its structural modification and modification to optimize performance, such as improving hydrophilicity, reducing toxicity, enhancing targeting, etc., to meet multiple clinical needs.
In the field of materials science, or because of its special chemical structure and properties, it has applications in the preparation of specific functional materials, such as the preparation of X-ray sensitive materials, for non-destructive testing, imaging technology related materials research and development. In short, this compound has important value and wide application prospects in the fields of medicine, scientific research and materials.
How safe is N, n '-bis (2,3-dihydroxypropyl) -5- [ (hydroxyacetyl) (2-hydroxyethyl) amino] -2,4,6-triiodobenzene-1,3-dicarboxamide?
This drug is called N, N '-bis (2,3-dihydroxypropyl) -5 - [ (hydroxyacetyl) (2-hydroxyethyl) amino] -2, 4, 6-triiodobenzene-1, 3-diformamide. The safety of this drug needs to be reviewed in detail.
Its metabolic process in the body is complex, and many metabolic links will affect safety. After oral intake, the first-pass effect will cause some drugs to be inactivated or transformed. If the metabolism is abnormal, or accumulated in the body, it will lead to adverse reactions. Entering the blood circulation, the degree of binding to plasma proteins is also related to safety. The binding rate is unstable, which will cause fluctuations in the concentration of free drugs. If the concentration is too high or the risk of toxic side effects is increased.
From a toxicological point of view, long-term or high-dose use, or damage to specific organs such as liver and kidney. Because of its iodine content, some individuals may be allergic to iodine. Before use, a detailed history of allergies should be consulted to prevent allergic reactions, ranging from rash and itching to anaphylactic shock, which is life-threatening.
In addition, when used in combination with other drugs, there may be interactions. If taken with certain nephrotoxic drugs, it may increase the risk of kidney damage. Therefore, when using this drug, the doctor should carefully check the patient's medical history and medication history, weigh the pros and cons, and closely monitor between medications to detect whether there are any adverse reactions, and treat it in a timely manner to ensure the safety of the patient's medication.
What are the advantages of N, n '-bis (2,3-dihydroxypropyl) -5- [ (hydroxyacetyl) (2-hydroxyethyl) amino] -2,4,6-triiodobenzene-1,3-dicarboxamide over other similar compounds?
N, N '-bis (2,3-dihydroxypropyl) -5- [ (hydroxyacetyl) (2-hydroxyethyl) amino] -2,4,6-triiodobenzene-1,3-diformamide, this is a rather unique chemical substance. Compared with other similar compounds, its advantages are full.
Bear the brunt, it has excellent water solubility. Just like a river can hold ten thousand streams, this compound is easily soluble in water due to its special molecular structure. In this way, in many reactions or applications that need to be carried out in an aqueous environment, there is no need to worry about dissolution problems, just like a boat in water, unobstructed, which greatly enhances the convenience of its application.
Furthermore, this compound exhibits a high degree of affinity for specific tissues or cells. Like a magnet attracting iron filings, it can precisely combine with certain tissues or cells. In the field of medical imaging, this property is invaluable, enabling doctors to observe specific parts more clearly and accurately, just like adding a sharp mirror to the doctor's eye, which is helpful for the early and accurate diagnosis of diseases.
Not only that, the stability of this compound is also outstanding. No matter how the temperature and pH of the external environment change, it can maintain the stability of its own structure and properties, just like a strong fortress, not afraid of wind and rain. This stability ensures that it will not easily deteriorate or decompose during storage and use, thus ensuring the quality and effect of the product.
From the perspective of Shi Zhi, N, N '-bis (2,3-dihydroxypropyl) -5- [ (hydroxyacetyl) (2-hydroxyethyl) amino] -2,4,6-triiodobenzene-1,3-diformamide has unique advantages over other similar compounds in terms of water solubility, affinity and stability. Like a shining star in the night sky, it shines uniquely in chemistry and related fields.
What is the production process of N, n '-bis (2,3-dihydroxypropyl) -5- [ (hydroxyacetyl) (2-hydroxyethyl) amino] -2,4,6-triiodobenzene-1,3-dicarboxamide?
To prepare N, N '-bis (2,3-dihydroxypropyl) -5- [ (hydroxyacetyl) (2-hydroxyethyl) amino] -2,4,6-triiodobenzene-1,3-diformamide, the preparation method is as follows:
Prepare various materials first, and the required materials should be carefully selected to ensure their purity. Among the materials, the key is a compound containing a benzene ring, which requires a specific substituent to meet the needs of the subsequent reaction.
In the cleaning vessel, the main reactant is first placed and dissolved with an appropriate amount of solvent. The choice of this solvent is related to the smoothness and inversion of the reaction, and is selected as one that is soluble with the reactants and does not hinder the reaction.
Then, slowly add specific reagents to initiate the reaction. When adding, the rate should be stable, not fast or slow, so as not to affect the reaction process. The temperature of the reaction also needs to be precisely controlled, either at room temperature or heated, depending on the characteristics of the reaction. When heating, use suitable equipment to raise the temperature evenly, so as not to overheat or overcool.
During the reaction, it is often necessary to stir to fully mix the reactants and promote the speed of the reaction. Looking at the reaction phenomenon, or the change of color, or the generation of precipitation, are all signs of the reaction process. When the reaction is appropriate, stop it with a suitable method.
After the product is separated and purified. Or use the method of filtration to remove its insoluble impurities; or use the technology of distillation to divide its different boiling points. After multiple purifications, pure N, N '-bis (2,3-dihydroxypropyl) -5- [ (hydroxyacetyl) (2-hydroxyethyl) amino] -2,4,6-triiodobenzene-1,3-diformamide. The whole process requires fine operation and attention to each step to achieve its work.
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