3 5 Bis Acetylamino 2 4 6 Triiodobenzoic Acid 1 Deoxy 1 Methylamino D Glucitol 1 1
Iodobenzene
3,5-bis(acetylamino)-2,4,6-triiodobenzoic Acid - 1-deoxy-1-(methylamino)-d-glucitol (1:1)
FAQ

What are the main uses of 3,5-bis (acetamido) -2,4,6-triiodobenzoic acid-1-deoxy-1- (methylamino) -D-glucitol (1:1)?

3% 2C5-bis (ethoxyhydroxyl) - 2% 2C4% 2C6-tribromobenzoic acid-1-deoxy-1- (ethoxycarbonyl) -D-furanogluconuronic acid (1:1) is a unique chemical compound that has important uses in many fields.

In the field of medicinal chemistry, it may act as a key intermediate to assist in the synthesis of drug molecules with specific pharmacological activities. Because the functional groups contained in it can participate in various chemical reactions, by ingeniously designing the synthesis path, it is expected to create new drugs with high affinity and selectivity for specific disease targets. For example, by virtue of the properties of the benzoic acid and glucuronic acid parts in its structure, it may play a positive role in pharmacokinetics and pharmacodynamics, or it may improve the absorption, distribution, metabolism and excretion of drugs, and improve the efficacy of drugs.

In the field of materials science, this compound may be used to prepare functional materials. Its complex structure may endow the material with special physical and chemical properties, such as being used to prepare adsorbent materials with selective adsorption or identification functions for specific substances. By the interaction between its functional groups and the target substance, efficient separation and enrichment can be achieved. Or it can be used as a monomer to participate in the polymerization reaction to prepare polymer materials with special properties, such as biodegradable or biocompatible polymers, which have potential application value in the field of biomedical engineering and environmentally friendly materials.

Furthermore, in the study of organic synthetic chemistry, it can be used as a model compound to explore new reaction mechanisms and synthesis methods. Researchers can develop novel organic synthesis strategies by optimizing its structure modification and reaction conditions, providing new ideas and methods for the development of organic chemistry, and promoting the continuous expansion and progress of the field of organic synthetic chemistry.

What are the side effects of 3,5-bis (acetamido) -2,4,6-triiodobenzoic acid-1-deoxy-1- (methylamino) -D-glucitol (1:1)

3% 2C5 - bis (ethoxy hydroxy) - 2% 2C4% 2C6 - tribromobenzoic acid - 1 - deoxy - 1 - (ethoxy hydroxy) - D - glucuronic acid (1:1) is a complex chemical compound, which is effective in many fields.

In the field of medicine, such compounds may exhibit antibacterial properties due to their unique chemical structures and properties. Groups such as ethoxy hydroxy and bromine atoms may interfere with bacterial cell wall synthesis, cell membrane function or key metabolic pathways, inhibit the growth and spread of common pathogens, and provide an opportunity for the development of new antibacterial drugs. At the same time, in terms of antivirus, it may be able to interact with viral surface proteins or host cell receptors to block the process of viral adsorption, invasion or replication, and contribute to the research and development of antiviral drugs. In addition, in the exploration of cancer treatment drugs, it may be able to regulate the cancer cell proliferation signaling pathway by virtue of specific structures, induce cancer cell apoptosis, and cause little damage to normal cells. It is expected to become an efficient and low-toxic anti-cancer drug.

In the field of materials science, this compound can be used as a functional additive. Due to its unique chemical structure, it may endow materials with special properties. For example, adding it to polymer materials may enhance material stability and antioxidant properties, because groups such as ethoxy hydroxyl groups can capture free radicals and delay material aging. It can also enhance the surface activity of materials, making it easier for materials to combine with other substances, and expand the application range of materials. Adding it to coatings can improve the film formation, wear resistance and corrosion resistance of coatings, injecting new vitality into the development of materials science.

In the agricultural field, it can be used as a new type of pesticide or plant growth regulator. With its antibacterial and antiviral properties, it can effectively prevent and control crop diseases and pests, reduce the use of chemical pesticides, and help the development of green agriculture. When used as a plant growth regulator, it can adjust the balance of plant hormones, promote plant growth and development, and improve crop yield and quality, which is of great significance to the sustainable development of agriculture.

What are the applicable populations of 3,5-bis (acetamido) -2,4,6-triiodobenzoic acid-1-deoxy-1- (methylamino) -D-glucitol (1:1)?

3% 2C5 - bis (ethoxyhydroxyl) - 2% 2C4% 2C6 - tribromobenzoic acid - 1 - deoxy - 1 - (methyl hydroxyl) - D - glucuronic acid (1:1) This drug is suitable for patients with specific inflammation and related metabolic disorders. Because it can regulate inflammatory mediators in the body and improve metabolic pathways, it is suitable for joint pain and swelling caused by inflammation, and accompanied by abnormal metabolic indicators, such as blood sugar and blood lipids.

However, pregnant women and breastfeeding women, due to their special physical conditions, the drug may have unknown harm to the fetus or infant, so this drug should not be used. Those who have a history of allergies to the ingredients of this medicine should also not be used, so as not to cause allergic diseases, such as rash, itching, and even life-threatening. Those with severe liver and kidney insufficiency should not be used because their body's ability to metabolize and excrete the drug is greatly reduced, and the drug or cause the drug to accumulate, and the toxic and side effects are aggravated.

When using this medicine, be sure to follow the doctor's advice. Do not increase or decrease the dose by yourself, so as not to affect the efficacy of the medicine or cause adverse reactions. During the medication, if there is any discomfort, seek medical attention immediately.

What are the storage conditions for 3,5-bis (acetamido) -2,4,6-triiodobenzoic acid-1-deoxy-1- (methylamino) -D-glucitol (1:1)?

The storage conditions of 3% 2C5-bis (ethoxycarbonyl) -2% 2C4% 2C6-tribromobenzoic acid-1-deoxy-1- (ethoxycarbonyl) -D-glucuronic acid (1:1) are crucial to whether this compound can maintain its chemical stability and biological activity.

This compound needs to be stored in a dry, cool and well-ventilated place. A dry environment can avoid adverse reactions such as hydrolysis caused by moisture. If the moisture is too heavy, it may cause changes in its molecular structure, which will affect its quality and efficacy. In cool conditions, the temperature should be maintained between 2-8 ° C. Excessive temperature may accelerate its chemical reaction rate, causing it to decompose and deteriorate; too low temperature may slow down the reaction rate, but in some cases it may cause its physical state to change, which also affects its properties.

At the same time, care should be taken to avoid light. Light can cause photochemical reactions, causing damage to the structure and activity of the compound. Storage should be selected in a dark place, or use light-shielding packaging materials to ensure its stability.

In addition, this compound should be stored separately to avoid mixing with other chemicals to prevent chemical reactions. When taking it, strict operating procedures should also be followed to maintain the stability of its storage conditions. In this way, 3% 2C5-bis (ethoxycarbonyl) -2% 2C4% 2C6-tribromobenzoic acid-1-deoxy-1- (ethoxycarbonyl) -D-glucuronic acid (1:1) can be ensured to maintain good quality and activity during storage.

What is the production process of 3,5-bis (acetamido) -2,4,6-triiodobenzoic acid-1-deoxy-1- (methylamino) -D-glucitol (1:1)?

To prepare 3% 2C5-bis (ethoxycarbonyl) - 2% 2C4% 2C6-tribromobenzoic acid - 1 - deoxy - 1 - (ethoxycarbonyl) - D - glucose ester (1:1), the preparation process is as follows:

First take an appropriate amount of raw materials and place the reaction substrate in a clean reactor. Under suitable temperature and pressure conditions, add a specific proportion of catalyst and solvent. The reaction temperature needs to be precisely regulated, not too high or too low, so as not to affect the reaction process and product purity. The pressure also needs to be maintained stable to ensure that the reaction environment is suitable.

During the reaction, closely observe the reaction phenomena, such as color changes, gas escape, etc. Through specific detection methods, monitor the reaction progress to determine whether the reaction has reached the expected stage.

After the reaction is completed, use suitable separation methods, such as extraction, distillation, recrystallization, etc., to separate and purify the product. Remove impurities and improve the purity of the product. During extraction, select a suitable extractant to ensure effective separation. During distillation, control the temperature and pressure to accurately obtain the target product. For recrystallization, select the appropriate solvent and conditions to precipitate the product in a pure crystal form.

Finally, after multiple processes, pure 3% 2C5-bis (ethoxycarbonyl) - 2% 2C4% 2C6-tribromobenzoic acid - 1 - deoxy - 1 - (ethoxycarbonyl) - D - glucose ester (1:1) can be obtained. The whole preparation process requires strict control of each link parameter to ensure the quality and yield of the product.