As a leading (4aR,4bS,6aS,7S,9aS,9bS,11aR)-4a,6a-Dimethyl-2-oxohexadecahydro-1H-indeno[5,4-f]quinoline-7-Carboxylic acid supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
What is the chemical structure of (4aR, 4bS, 6aS, 7S, 9aS, 9bS, 11aR) -4a, 6a-dimethyl-2-oxohexadecyl-1H-indo [5,4-f] quinoline-7-carboxylic acid?
This compound is an organic compound with a complex structure, according to its name ((4aR, 4bS, 6aS, 7S, 9aS, 9bS, 11aR) -4a, 6a-dimethyl-2-oxoctadecyl-1H-phenanthrene [5,4-f] pyran-7-carboxylic acid), and its structural characteristics can be gradually analyzed.
Looking at the markers of its chiral center (4aR, 4bS, etc.), this indicates that the specific carbon atom in the compound molecule has a specific three-dimensional configuration. "4a, 6a-dimethyl", it is apparent that there is a methyl group attached to each of the carbon atoms at the 4a and 6a positions. " "2-oxo" means that the atom at position 2 is an oxygen atom, and this oxygen atom is connected to the surrounding atoms in a specific way to form a carbonyl-like structure. "Octadecyl hydrogen" indicates that there are eighteen hydrogen atoms in the corresponding position in the mother nuclear structure of the entire molecule. "1H-phenanthrene [5,4-f] pyran" reveals that its core skeleton is formed by a specific combination of phenanthrene and pyran rings (5,4-f). And "7-carboxylic acid" indicates that there is a carboxyl functional group attached to the carbon atom at position 7.
Overall, the structure of this compound is composed of a polycyclic skeleton with a specific chiral configuration, and functional groups such as methyl, carbonyl, and carboxyl groups connected to a specific position in the skeleton, presenting a unique spatial arrangement and chemical characteristics.
What are the physical properties of (4aR, 4bS, 6aS, 7S, 9aS, 9bS, 11aR) -4a, 6a-dimethyl-2-oxohexadecyl-1H-indo [5,4-f] quinoline-7-carboxylic acid?
(4aR, 4bS, 6aS, 7S, 9aS, 9bS, 11aR) -4a, 6a-dimethyl-2-oxoctadecyl-1H-indeno [5,4-f] pyran-7-carboxylic acid This compound has the following physical properties:
Its appearance is often white to white solid state, which is a common external characterization of many organic compounds. In terms of solubility, it exhibits specific solubility properties in common organic solvents. For example, easily soluble in halogenated hydrocarbon solvents such as dichloromethane, dichloromethane has good solubility. The chlorine atom in the molecular structure makes it have a certain polarity, and there is a suitable interaction with the compound molecule, so that it can be effectively dispersed and dissolved. It also has a certain solubility in methanol. The hydroxyl group of methanol can interact with some groups in the compound to form hydrogen bonds, etc., to help dissolve. However, in non-polar solvents such as n-hexane, the solubility is poor, because the non-polar long carbon chain structure interacts weakly with the polar part of the compound.
The melting point is also an important physical property. The melting point is in a certain temperature range, and the specific value is affected by factors such as the purity of the compound and the crystalline morphology. During the heating process, the lattice energy can be overcome, and the solid state transitions to the liquid state. The boiling point reflects the energy required for its liquid state to transform into a gas state. The boiling point of the compound shows a corresponding value under specific pressure conditions, reflecting the size of the intermolecular force.
The density of this compound is relatively fixed, which is a characteristic parameter of the substance, and is less affected by temperature and pressure. This parameter has reference value in chemical production, material separation and other fields. In addition, its refractive index also has characteristic values, and the refractive index is closely related to the molecular structure and intermolecular arrangement, which can be used for purity detection and compound identification.
What is the main use of (4aR, 4bS, 6aS, 7S, 9aS, 9bS, 11aR) -4a, 6a-dimethyl-2-oxohexadecyl-1H-indo [5,4-f] quinoline-7-carboxylic acid?
(4aR, 4bS, 6aS, 7S, 9aS, 9bS, 11aR) -4a, 6a-dimethyl-2-oxo-octadecyl-1H-anthracene [5,4-f] pyran-7-carboxylic acid, what are its main uses? This substance has important uses in many fields such as medicine and chemical industry.
In the field of medicine, it may be possible to develop new drugs with its special chemical structure and activity. It may act on specific biological targets and be beneficial to the treatment of diseases. For example, some compounds with similar structures can be used in the development of anti-tumor drugs, inhibiting the growth and proliferation of tumor cells by interfering with the metabolism or signal transduction pathways of tumor cells. This compound may also play a role in the research and development of anti-inflammatory drugs, reducing inflammation by regulating inflammation-related signaling pathways in the body.
In the chemical industry, it can be used as an intermediary for organic synthesis. With its unique chemical properties, it is converted into other high-value-added chemicals through specific chemical reactions. It can participate in polymerization reactions to prepare polymer materials with special properties, such as polymers with excellent heat resistance and corrosion resistance, which are used in aerospace, automobile manufacturing and other industries that require strict material properties. It can also be used in fragrance synthesis to give the product a unique aroma and add its commercial value.
However, the specific use needs to be determined accurately according to the detailed physical and chemical properties, biological activity research and practical application tests of the compound.
What are the synthesis methods of (4aR, 4bS, 6aS, 7S, 9aS, 9bS, 11aR) -4a, 6a-dimethyl-2-oxohexadecyl-1H-indo [5,4-f] quinoline-7-carboxylic acid?
Wen Jun inquired about the synthesis method of\ ((4aR, 4bS, 6aS, 7S, 9aS, 9bS, 11aR) -4a, 6a-dimethyl-2-oxoctadecyl-1H-phenyl [5,4-f] furan-7-carboxylic acid\). The synthesis method of this compound is quite complicated and often requires multiple steps to react.
When starting, or choose a suitable starting material, this raw material needs to have a functional group that can be derived from the target structure. For example, compounds with similar structures such as benzene rings and furan rings can be selected as starting points.
In the process of synthesis, many organic reactions are often involved. Such as alkylation reaction, methyl and other alkyl groups can be introduced to form the structure of\ (4a, 6a-dimethyl\). Or use halogenated alkanes and suitable nucleophiles, under the catalysis of bases, to carry out alkylation reaction.
Or involve oxidation reaction to construct the structure of\ (2-oxo\). Suitable oxidizing agents, such as Jones reagent, can be used to oxidize specific alcohol structures to obtain corresponding carbonyl groups.
Cyclization reaction is also key to construct the fused ring structure of phenyl furan. Or through reactions such as nucleophilic substitution and condensation in molecules, after appropriate conditions, form a target fused ring. < Br >
And between each step of the reaction, the reaction conditions need to be carefully controlled. Such as temperature, reaction time, proportion of reactants, choice of solvent, etc., all affect the process of the reaction and the purity of the product.
After each step of the reaction, it is often necessary to separate and purify the product. Column chromatography, recrystallization and other methods can be used to obtain a pure product, which is convenient for the next step of the reaction.
Synthesis of this compound requires deep knowledge of organic synthesis and fine experimental operations to obtain the target product.
What is the market outlook for (4aR, 4bS, 6aS, 7S, 9aS, 9bS, 11aR) -4a, 6a-dimethyl-2-oxohexadecyl-1H-indo [5,4-f] quinoline-7-carboxylic acid?
Guanfu (4aR, 4bS, 6aS, 7S, 9aS, 9bS, 11aR) -4a, 6a-dimethyl-2-oxooctadecyl-1H-phenanthrene [5,4-f] xanthene-7-carboxylic acid, its market prospects are quite complex, and it needs to be examined in detail from various angles.
From the perspective of use, this compound may have applications in various fields such as medicine and chemical industry. In the field of medicine, or can be used as a pharmaceutical intermediate, through chemical modification to create novel and curative drugs. In the chemical industry, it may be able to develop its functions in the synthesis of materials, such as the preparation of polymer materials with special properties, thus broadening its market domain.
In terms of market demand, with the advancement of pharmaceutical technology, the demand for new drug intermediates may be on the rise. If this compound shows good activity and potential in the process of drug research and development, pharmaceutical companies must have demand for its raw material supply, which will open up a considerable market space for it. The vigorous development of the chemical industry will also generate demand for unique compounds required for the synthesis of special materials, or lead to an increase in demand for this substance.
However, there are also challenges in the market outlook. The difficulty of the synthesis process has a profound impact on the cost. If the process of synthesizing this compound is complicated and the conditions are harsh, the cost will be high, which will weaken its market competitiveness. And peer competition should not be underestimated. If others have developed alternatives with similar functions and low cost, it may have an impact on their market share.
In summary, (4aR, 4bS, 6aS, 7S, 9aS, 9bS, 11aR) -4a, 6a-dimethyl-2-oxoctadecyl-1H-phenyl [5,4-f] xanthene-7-carboxylic acid market prospects Although there are opportunities, challenges also arise. Only by properly responding can we seek opportunities for development in the market.