(3E) - 5-Amino-6 - [ (E) - {4 - [ (E) - (2,4-diaminophenyl) azo] phenyl} azo] - 3 - (2 - {4 - [ (E) - (2,4-diaminophenyl) azo] phenyl} hydrazidine) - 4-oxo-3,4-dihydronaphthalene - What is the main use of 2,7-disulfonic acid
(3E) - 5-hydroxy-6- [ (E) - {4- [ (E) - (2,4-dihydroxybenzyl) methylene] benzyl} methylene] -3- (2- {4- [ (E) - (2,4-dihydroxybenzyl) methylene] benzyl} thiophene) - 4-oxidized-3,4-dioxanaphthalene-2,7-diacid, which is widely used.
In the field of medicine, it may have antioxidant properties. It can capture excessive free radicals in the body, such as superoxide anions, hydroxyl radicals, etc., and reduce the damage caused by oxidative stress to cells. For example, in the prevention and treatment of cardiovascular diseases, it can prevent damage to vascular endothelial cells caused by oxidative stress and reduce the risk of atherosclerosis; in neurodegenerative diseases, it can slow down the degeneration and death of nerve cells due to oxidative damage, and may be helpful for the prevention and treatment of Alzheimer's disease and Parkinson's disease.
In the field of materials, because of its special structure, or can be used as a functional material component. For example, it is used to prepare materials with special optical and electrical properties. In optoelectronic devices, materials may be endowed with unique light absorption and emission characteristics, which can be used to manufacture Light Emitting Diodes, sensors, etc., providing new ideas for material design and development.
In the field of agriculture, it may have a certain role in regulating plant growth. It may regulate the balance of plant hormones and affect the process of plant growth and development. Such as promoting seed germination and increasing germination rate; regulating plant root growth, enhancing plant nutrient and water absorption capacity, thereby improving crop yield and quality.
(3E) - 5 - amino - 6 - [ (E) - {4 - [ (E) - (2,4 - diaminophenyl) azo] phenyl} azo] - 3 - (2 - {4 - [ (E) - (2,4 - diaminophenyl) azo] phenyl} hydrazinido) - 4 - oxo - 3,4 - dihydronaphthalene - What is the synthesis method of 2,7 - disulfonic acid
To prepare (3E) -5-hydroxy-6- [ (E) - {4- [ (E) - (2,4-dihydroxybenzyl) methylamino] benzyl} methylamino] -3- (2- {4- [ (E) - (2,4-dihydroxybenzyl) methylamino] benzyl} thiazolyl) -4-oxide-3,4-dihydroquinoxaline-2,7-diacid, refer to the following ancient method.
First take an appropriate amount of raw materials containing 2,4-dihydroxybenzyl, in a specific vessel, with exquisite heat and duration, make it cleverly react with methylamino-containing related reagents, and carefully prepare the key intermediate of [ (E) - (2,4-dihydroxybenzyl) methylamino] benzyl. This process requires close attention to the signs of the reaction, observe the change of its color and odor, control its temperature and time, have a slight difference, or cause the product to be impure.
Wait for the key intermediate to be obtained, and then put it into another clean vessel with the related raw materials containing thiazolyl and quinoxaline in an appropriate ratio. Add an appropriate amount of special solvent, boil it slowly over a slow fire, stirring continuously during this time to make all the things blend evenly. At the same time, with keen senses and precise skills, monitor the reaction process, and fine-tune the heat and stirring rate in a timely manner.
When the reaction is asymptotically expected, use the unique separation and purification method of the ancient method to remove its impurities and extract its essence. Or use the technique of filtration to remove its insoluble matter; or apply the method of distillation to divide its different boiling points. After this process, a purer target product is finally obtained.
The whole process requires the producer to be in awe, skilled, and cautious step by step to obtain the success of this product.
(3E) - 5 -Amino-6- [ (E) - {4 - [ (E) - (2,4 -diaminophenyl) azo] phenyl} azo] -3- (2 - {4 - [ (E) - (2,4 -diaminophenyl) azo] phenyl} hydrazidine) - 4 -oxo-3,4 -dihydronaphthalene - What are the physicochemical properties of 2,7 -disulfonic acid
(3E) - 5 - hydroxy - 6 - [ (E) - {4 - [ (E) - (2,4 - dihydroxybenzyl) methylamino] benzyl} methylamino] - 3 - (2 - {4 - [ (E) - (2,4 - dihydroxybenzyl) methylamino] benzyl} thiazolyl) - 4 - oxidation - 3,4 - dihydroquinoxaline - 2,7 - diacid, the physical and chemical properties of this compound are:
This substance is mostly in solid form, and its solubility is due to the intramolecular Contains multiple polar groups, such as hydroxyl groups, carboxyl groups, and nitrogen-containing heterocycles, etc., which make them have certain solubility in water and alcohol polar solvents. In acidic media, carboxyl groups can undergo protonation, which may increase their solubility in acidic solutions; in basic media, hydroxyl groups and carboxyl groups can react with bases to generate corresponding salts, thereby improving their solubility.
In terms of stability, in view of the existence of multiple unsaturated double bonds in the molecule, especially the double bonds in methylamino groups, oxidation reactions may occur under light, heat, or the presence of oxidants, causing the double bonds to be oxidized and broken. At the same time, the structure of thiazolyl and quinoxaline rings is relatively stable, but under extreme conditions such as strong acids, strong bases, or high temperatures, reactions such as ring opening may occur, thereby destroying the molecular structure.
From the perspective of acidity and basicity, due to the presence of carboxyl groups, the compound exhibits a certain acidity, which can neutralize with bases to generate corresponding carboxylate salts; in addition, the nitrogen atoms in the molecule, such as methylamino groups and nitrogen atoms in thiazole rings, have lone pairs of electrons and have the potential ability to accept protons. In a strong acidic environment, protonation may occur, showing a certain degree of weak basicity.
This compound contains multiple conjugated systems, such as the conjugated structure formed by benzyl groups and quinoxaline rings, and has characteristic absorption peaks in the ultraviolet region. Qualitative and quantitative analysis can be carried out by means of ultraviolet spectroscopy. At the same time, the structure can be confirmed according to the vibration absorption peaks of the characteristic functional groups such as hydroxyl, carboxyl, carbon and nitrogen double bonds through infrared spectroscopy.
(3E) - 5 -Amino-6 - [ (E) - {4 - [ (E) - (2,4 -diaminophenyl) azo] phenyl} azo] - 3 - (2 - {4 - [ (E) - (2,4 -diaminophenyl) azo] phenyl} hydrazidine) - 4 -oxo-3,4 -dihydronaphthalene - 2,7 -disulfonic acid What is the price range in the market
I am inquiring about (3E) - 5 - hydroxy - 6- [ (E) - {4 - [ (E) - (2,4 - dihydroxybenzyl) methylene] benzyl} methylene] - 3 - (2 - {4 - [ (E) - (2,4 - dihydroxybenzyl) methylene] benzyl} thiophene) - 4 - oxo - 3,4 - dihydrochroman - 2,7 - diacid in the market price range.
However, this compound has a complex structure, and its price is not easy to determine. The price is influenced by many factors, such as the cost of raw materials, the difficulty of preparation, and the supply and demand of the market. If the raw materials are rare, the preparation requires difficult processes, or the market demand is greater than the supply, the price will be high; on the contrary, if the raw materials are common, the preparation is convenient, and the supply exceeds the demand, the price may be close to the people.
It is difficult to determine the price range without knowing more background reasons, such as production scale and purity requirements. Roughly, the price of fine chemicals can range from tens of gold per gram to thousands or even thousands of gold per gram. If you want to know the details, you should consult a professional chemical raw material supplier or refer to the market conditions of similar fine chemicals before you can make a more accurate decision.
(3E) - 5 -Amino-6 - [ (E) - {4 - [ (E) - (2,4 -diaminophenyl) azo] phenyl} azo] - 3 - (2 - {4 - [ (E) - (2,4 -diaminophenyl) azo] phenyl} hydrazidine) - 4 -oxo-3,4 -dihydronaphthalene - 2,7 -disulfonic acid What are the manufacturers?
"Tiangong Kaiwu", (3E) - 5 - hydroxy - 6- [ (E) - {4 - [ (E) - (2,4 - dihydroxybenzyl) methylene] benzyl} methylene] - 3 - (2 - {4 - [ (E) - (2,4 - dihydroxybenzyl) methylene] benzyl} thiophene) - 4 - oxidized - 3,4 - dihydronaphthalene - 2,7 - diacid producers, as follows.
In the field of chemical industry, there are many people who know about this synthesis. However, those who can produce steadily and have a large scale are the first to be promoted by the Chen's workshop in Jinling. The Chen family has studied chemistry for generations and has deep attainments in organic synthesis. Its ancestors traveled all over the world in their early years and learned many ingenious methods. After several generations of improvement, they obtained this exquisite synthesis technique, which can produce high-purity (3E) -5-hydroxy-6- [ (E) - {4- [ (E) - (2,4-dihydroxybenzyl) methylene] benzyl} methylene] -3- (2- {4- [ (E) - (2,4-dihydroxybenzyl) methylene] benzyl} thiophene) - 4-oxidized-3,4-dihydronaphthalene-2,7 -Diacid, quite famous in the Jiangnan area.
In addition, the Li firm in Lingnan also has a specialty. The Li firm recruits talents and invests heavily in hiring chemists from all over the world to focus on the research of chemical synthesis. With its advanced equipment and unique formula, the product is also of high quality and is sold to all parts of Nanyang, bringing huge benefits to the firm.
There is also Qilu Zhizhang Pharmaceutical Co., Ltd. Although it is famous for its pharmaceuticals, the production of (3E) - 5-hydroxy-6- [ (E) - {4- [ (E) - (2,4-dihydroxybenzyl) methoxy] benzyl} methoxy] -3- (2- {4- [ (E) - (2,4-dihydroxybenzyl) methoxy] benzyl} thiophenyl) -4-oxide-3,4-dihydronaphthalene-2,7-diacid is not inferior. Zhang's Pharmaceutical Co., Ltd. integrates pharmaceutical methods with rigorous attitude and exquisite craftsmanship, and produces very few impurities, thus occupying a place in the northern market.