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What is the chemical structure of ethyl (3S) -9,10-difluoro-3-methyl-7-oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxylate?
This is the problem of describing the chemical structure of a substance. To solve the chemical structure of this substance, it is necessary to analyze the clues contained in its name in detail.
Its name is "ethyl (3S) -9,10-dihydro-3-methyl-7-oxo-2,3-dihydro-7H - [1,4] oxazino [2,3,4-ij] xanthon-6-carboxylic acid ethyl ester".
"ethyl" expressly indicates that this substance contains ethyl ester group, which is a common chemical group with a structure of -COOCH -2 CH.
" (3S) " indicates that the three-dimensional configuration of the specific position (position 3) of this molecule is S-type.
"9,10-dihydro" means that the double bonds at positions 9 and 10 in the molecule are hydrogenated to form a single bond.
"3-methyl" indicates that position 3 is connected to methyl-CH.
"7-oxo" indicates that position 7 has a carbonyl C = O.
"2,3-dihydro" means that the double bonds at positions 2 and 3 are also hydrogenated to form a single bond.
"7H - [1,4] oxazino [2,3,4 - ij] xanthon" describes the core cyclic structure of this molecule, which is formed by fusing the [1,4] oxazine ring with the xanthon ring.
"6-Ethyl carboxylate" Table 6 contains -COOH and ethanol esterified -COOCH -2 CH group.
In summary, the chemical structure of this compound is based on [1,4] oxazino [2,3,4-ij] xanthon as the core skeleton, with methyl group and specific S configuration at position 3, carbonyl group at position 7, ethyl ester at position 6, and partial double bond hydrogenation at positions 9, 10 and 2 and 3. Its structure is complex, and each group is connected to each other to co-form this unique chemical structure.
What are the physical properties of ethyl (3S) -9,10-difluoro-3-methyl-7-oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxylate?
(3S) - 9,10 - dihydro - 3 - methyl - 7 - oxo - 2,3 - dihydro - 7H - [1,4] diazonaphthaleno [2,3,4 - ij] xanthon - 6 - ethyl carboxylate is an organic compound. Its physical properties are complex, and are described as follows:
Looking at its properties, it is either a crystalline solid under normal conditions, and may also be powdery, colored or nearly colorless, or slightly yellow, with a fine texture, depending on the synthesis conditions and purity.
When it comes to melting point, this compound has a specific melting point, but the exact value varies slightly due to the preparation process and the influence of impurities, and is roughly in a certain temperature range. This temperature range is of great significance for identification and purity determination. Under a specific thermal environment, the intermolecular forces change, the lattice structure disintegrates, and the phase transition occurs.
In terms of boiling point, because of its structure, there are various chemical bonds and functional groups, and the intermolecular forces are complex, resulting in a high boiling point. To make it boil, sufficient energy needs to be supplied to overcome the attractive forces between molecules and realize the transition from liquid to gaseous state.
Solubility is also an important property. In organic solvents, such as ethanol and acetone, its solubility is acceptable by virtue of the principle of similar miscibility. Due to the interaction between organic solvents and the molecules of the compound, van der Waals forces, hydrogen bonds, etc. can be formed to help it disperse and dissolve. However, in water, due to the poor matching of molecular polarity and water molecules, the solubility is not good.
Density is the mass per unit volume. The density of the compound depends on the molecular weight and the way of packing, and is related to the temperature and pressure. Under standard conditions, there is a relatively stable density value, which is crucial for material measurement and process design.
Refractive index characterizes the refractive properties of light when passing through the substance, and is related to the molecular structure and electron cloud distribution. Accurate refractive index data can be used for purity analysis and structural identification. Light propagates in it, and the propagation direction and speed change due to the action of molecules on light.
The physical properties of this compound are of great significance in the fields of organic synthesis and drug development. During synthesis, according to its melting point, solubility and other properties, the reaction conditions can be optimized, and the separation and purification methods can be selected. In drug development, solubility and stability are related to drug absorption, distribution and metabolism, providing a key basis for the creation of new drugs.
What is ethyl (3S) -9,10-difluoro-3-methyl-7-oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxylate?
I don't know what you said about the use of "ethyl (3S) -9,10-dihydro-3-methyl-7-oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] ethyl pyran-6-carboxylate". This is a complex organic compound whose use often depends on its chemical properties and reactivity.
Or in the field of medicine, such compounds can be exquisitely designed and synthesized to have specific biological activities and can be used as key intermediates in drug development. Because the fine regulation of the structure of organic molecules can affect their interaction with targets in vivo, it may be used to create new drugs that are effective for specific diseases or physiological processes. < Br >
In the field of materials science, it may endow materials with unique properties due to its special structure. Such as participating in the synthesis of polymer materials, changing the physical and chemical properties of materials, such as thermal stability, mechanical properties, optical properties, etc., and then applying to the preparation of advanced materials, such as high-performance plastics, optical materials, etc.
Or in the field of organic synthetic chemistry, as an important synthetic building block. Due to its specific functional groups and structures, it can construct more complex and functional organic molecules through various chemical reactions, promote the development and innovation of organic synthesis methodologies, and provide an effective way for the preparation of various organic compounds.
However, the exact use still needs to be detailed in professional chemical literature, research reports, or consult experts in the field of chemistry to clarify.
What are the synthesis methods of ethyl (3S) -9,10-difluoro-3-methyl-7-oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxylate?
To prepare (3S) -9,10-dihydro-3-methyl-7-oxo-2,3-dihydro-7H - [1,4] diazonaphthalene [2,3,4-ij] quinoxaline-6-carboxylate ethyl ester, there are many methods, each has its advantages and disadvantages, and varies according to different raw materials and conditions.
There are common aromatic hydrocarbons that start with common aromatics, are added by halogenation, and then condensed with amines to obtain key middle bodies. After hydrogenation, oxidation and other changes, the group is adjusted to obtain the target. The raw materials are easily available in this way, but the yield may be limited. < Br >
It also starts with nitrogen-containing heterocycles, and through cyclization reaction, the core structure is constructed, and then it is modified by substitution to form the target molecule. The reaction route is simple, and the atomic economy is good, but the raw materials may be rare and the conditions may be harsh.
Another biological enzyme catalysis method uses enzyme specificity and high efficiency to obtain products at mild places, which is green and environmentally friendly, but the enzyme cost is high and the stability needs to be improved.
The art of organic synthesis requires weighing raw materials, cost, yield, and environmental protection. Experimenters should optimize parameters according to their own conditions and goals to achieve good results. Or a small test first, observe the reactivity and yield, adjust the conditions according to the results, or combine the number method, take the length to avoid the short, and form the preparation of this compound.
What are the safety precautions for ethyl (3S) -9,10-difluoro-3-methyl-7-oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] quinoline-6-carboxylate?
"Tiangong Kaiwu" is a scientific and technological masterpiece written by Song Yingxing in the Ming Dynasty, but I don't know "ethyl + (3S) -9,10-dihydro-3-methyl-7-oxo-2,3-dihydro-7H- [1,4] oxazino [2,3,4-ij] xanthon-6-carboxylic acid ethyl ester". If it is about the safety precautions of this thing, let me tell you in ancient words.
This thing is not only a fine product of chemical synthesis, but its safety needs more attention. First, it is related to toxicity. Or it has unknown toxicity. When exposed, avoid it from entering the body, do not let the skin touch it, do not smell its breath, and do not import it. If you accidentally touch it, rinse it with water as soon as possible. If you feel unwell, seek medical help as soon as possible.
Second, it is related to ignition and explosion. Chemical substances are often at risk of ignition and explosion. This substance may be sensitive to heat and open flames. Keep away from fire and heat sources and store in a cool and ventilated place. Do not keep it in a high temperature environment to prevent ignition and explosion.
Third, it is related to storage. According to its characteristics, choose a suitable container for storage, seal it tightly to prevent it from leaking. And do not mix with other things to prevent reaction.
Fourth, it is related to operation. If you need to operate this object, be prepared with protective equipment, such as gloves, goggles, etc., operate according to precise methods, and do not act recklessly. After operation, it should also be properly cleaned without leaving hidden dangers.
Although I have said it in ancient times, the specific safety matters of this object need to be carefully investigated in accordance with modern scientific research and chemical regulations to ensure that nothing goes wrong.