What is the chemical structure of 1-n, 3-n-bis (2,3-dihydroxypropyl) -5- [ (2-hydroxyacetyl) amino] -2,4,6-triiodobenzene-1,3-dicarboxamide?
This is the name of the chemical substance. To clarify its chemical structure, it should be analyzed according to the system nomenclature. "1 - n% 2C3 - n - bis% 282% 2C3 - dihydroxypropyl% 29 - 5 -% 5B% 282 - hydroxyacetyl%29amino%5D - 2% 2C4% 2C6 - triiodobenzene - 1% 2C3 - dicarboxamide", first look at the main body, "2,4,6 - triiodobenzene - 1,3 - dicarboxamide", it can be seen that the main body is a benzene ring, with diformamide groups at the 1st and 3rd positions of the benzene ring, and iodine atoms at the 2nd, 4th, and 6th positions.
Look at the substituent again, "1 - n% 2C3 - n - bis% 282% 2C3 - dihydroxypropyl% 29", which means that there are two 2,3 - dihydroxypropyl groups attached to the nitrogen atom at the 1st and 3rd positions. And "5 -% 5B% 282 - hydroxyacetyl%29amino%5D" indicates that there is an (2 - hydroxyacetyl) amino group attached to the 5th position of the benzene ring.
In summary, the structure of this chemical substance takes the benzene ring as the core, and the benzene ring is connected with specific substituents, diformamide group, iodine atom, dihydroxypropyl group and (2-hydroxyacetyl) amino group according to their positions, thus forming a complex chemical structure.
What are the main uses of 1-n, 3-n-bis (2,3-dihydroxypropyl) -5- [ (2-hydroxyacetyl) amino] -2,4,6-triiodobenzene-1,3-dicarboxamide?
1 -\ (n\%\), 3 -\ (n\) -bis (2,3-dihydroxypropyl) - 5 - [ (2-hydroxyacetyl) amino] - 2,4,6-triiodobenzene-1,3-diformamide, an organic compound with a wide range of uses.
In the field of medical imaging, this compound is often used as a contrast agent. In X-rays, CT and other examinations, contrast agents can improve the contrast between tissues and organs, making imaging clearer and helping doctors accurately detect lesions. For example, during angiography, it is injected into blood vessels to make blood vessels clearly visible in the image, which is conducive to the diagnosis of vascular diseases.
At the scientific level, this compound can be used as an intermediate for chemical research. Chemists have created new compounds with specific properties through the modification and derivatization of their chemical structures, providing key basic substances for the exploration of drug development, materials science and many other fields.
In industrial production, it may be used in the synthesis of some special materials. With its unique chemical structure, it endows materials with specific properties, such as improving the stability of materials and improving the optical properties of materials, etc., to meet the needs of different industrial scenarios.
In summary, 1-\ (n\%\), 3-\ (n\) -bis (2,3-dihydroxypropyl) -5- [ (2-hydroxyacetyl) amino] -2,4,6-triiodobenzene-1,3-diformamide plays an important role in many aspects of medicine, scientific research and industry, and is of great significance to promote the development of related fields.
How safe is 1-n, 3-n-bis (2,3-dihydroxypropyl) -5- [ (2-hydroxyacetyl) amino] -2,4,6-triiodobenzene-1,3-dicarboxamide?
1 - n% 2C3 - n - bis (2,3 - dihydroxypropyl) - 5 - [ (2 - hydroxyacetyl) amino] - 2,4,6 - triiodobenzene - 1,3 - diformamide, the safety of this substance is related to many aspects.
In terms of its chemical structure, it contains triiodobenzene and many special groups. The iodine-containing structure may cause allergic reactions in some individuals, because it may be misjudged by the immune system as foreign matter, causing allergic symptoms, mild rash, itching, severe breathing difficulties and shock.
From the perspective of its production process, if the process is not properly controlled, impurities will remain or affect safety. If the raw materials and catalysts used in synthesis are not removed, or toxic, they are harmful to the human body.
Application scenarios are also key. If used in medical imaging, its metabolism and distribution in the body are crucial. Although it is designed to develop in a specific part, if it cannot be excreted in time, it will accumulate or damage organ function for a long time, such as increased burden on the kidneys, resulting in abnormal kidney function.
In addition, although animal experiments can provide some reference, human and animal physiology are different, and the results should be extrapolated to humans with caution. Clinical studies are also necessary to comprehensively evaluate its safety in humans, such as adverse reactions at different doses, and effects on different populations (young and old, pregnant women, and other special groups).
Overall, 1-n% 2C3-n-bis (2,3-dihydroxypropyl) -5- [ (2-hydroxyacetyl) amino] -2,4,6-triiodobenzene-1,3-diformamide The safety of this product needs to be comprehensively studied in many aspects, and its safety for specific uses can only be determined after rigorous evaluation.
What is the production method of 1-n, 3-n-bis (2,3-dihydroxypropyl) -5- [ (2-hydroxyacetyl) amino] -2,4,6-triiodobenzene-1,3-dicarboxamide?
1 -\ (n\),\ (3 - n -\) bis\ ((2\),\ (3 -\) dihydroxypropyl\ () - 5 - [ (2 -\) hydroxyacetyl\ () \) amino \()] - 2\),\ (4\),\ (6 -\) triiodobenzene\ (-1\),\ (3 -\) diformamide, the preparation method of this substance has been based on specific methods throughout the ages.
At the beginning, benzene was often used as a base, and after many delicate changes, iodine atoms were introduced. First, iodine and catalytic substances are used to add iodine groups to the benzene ring to obtain iodine-containing benzene. This step requires strict control of conditions, such as temperature, pressure, and the amount of catalyst. If there is a slight difference in the pool, the reaction results will be different.
Then, in the iodine-containing benzene ring, a carboxyl group is introduced. Or a strong oxidizing agent, or a specific reaction path is used to side-chain the benzene ring into a carboxyl group. This change also requires fine regulation to ensure that the position of carboxyl group introduction is accurate.
Furthermore, the carboxyl group is converted into the state of dicarbonamide. With ammonia and specific reaction conditions, the carboxyl group is cleverly combined with ammonia to form a dicarbonamide structure. In this step, it is also necessary to pay attention to the rate and degree of the reaction, so as not to overdo or underdo it.
As for\ (n\),\ (3 - n -\) bis\ (2\),\ (3 -\) dihydroxypropyl\ () \) and\ (5 - [ (2 -\) hydroxyacetyl\ () \) amino\ () ], all follow the wonderful method of organic synthesis. Choose the appropriate reagent, in sequence, at a specific position of the benzene ring, and combine it with a delicate reaction. Each step is related to the success or failure of the whole, and careful study is required to obtain a pure product. During the whole process of preparation, the experimenter needs to be careful, observe the changes in the reaction of each step in detail, and fine-tune the conditions according to the situation before obtaining the good product of this compound.
What are the advantages of 1-n, 3-n-bis (2,3-dihydroxypropyl) -5- [ (2-hydroxyacetyl) amino] -2,4,6-triiodobenzene-1,3-dicarboxamide over other similar products?
1 - n, 3 - n - bis (2, 3 - dihydroxypropyl) -5 - [ (2 - hydroxyacetyl) amino] -2, 4, 6 - triiodobenzene - 1, 3 - diformamide, this is a special chemical substance. Compared with other similar products, its advantages are significant, and listen to me in detail.
First, in the imaging performance end, this substance is excellent. Its triiodide structure can efficiently absorb X-rays, making imaging clearer and more accurate. In terms of medical imaging, clear images can help doctors keenly understand the details of the lesion, just like the doctor's eye, accurately locate the disease, greatly improve the accuracy of diagnosis, and pave a solid way for subsequent treatment.
Second, from the perspective of safety, it also has extraordinary things. The introduction of many hydrophilic groups such as hydroxyl groups and amide groups into its molecules greatly enhances the solubility in water. In this way, after entering the human body, it can be quickly dispersed, reducing the stimulation and adverse reactions to human tissues. Like warm water, it quietly merges into the human body without causing violent waves, adding a guarantee for patient safety.
Furthermore, in terms of stability, the substance performs well. Its unique chemical structure endows it with good stability, and it is not easy to deteriorate due to external factors during storage and use. Just like a sturdy fortress, it can still maintain its inherent characteristics after years and environmental changes, ensuring consistent product quality.
With its excellent imaging performance, high safety and good stability, this substance stands out in congeneric products, and will definitely shine in the field of medical imaging and make extraordinary contributions to human health.