Chemical Formula | C23H22F2N2O6S |
Molecular Weight | 494.49 |
Physical State | Solid (usually) |
Appearance | Typically a powder or crystalline solid |
Solubility In Water | Low solubility |
Solubility In Organic Solvents | Soluble in some organic solvents like DMSO, chloroform |
Melting Point | Specific value would require experimental determination |
Pka Value | Specific pKa values for acidic and basic groups would depend on the functional groups in the molecule |
Logp | Value indicating lipophilicity, would need experimental determination |
What is the chemical structure of 2- [2,6-Difluorobenzyl] Ethoxycarbonylamino] -4- [Dimethylaminomethyl] -5-4-Nitrophenylthiophene-3-Carboxylic acid?
This is the naming of an organic compound. To clarify its chemical structure, it is necessary to follow the naming rules of organic chemistry.
"2- [2,6-difluorobenzyl] ethoxycarbonyl amino-4- [dimethylaminomethyl] -5- (4-nitrophenyl) thiophene-3-carboxylic acid", from its name, this compound has a thiophene ring as the core structure. The second position of the thiophene ring is connected with a substituent containing [2,6-difluorobenzyl] ethoxycarbonyl amino group. In this substituent, the ethoxycarbonyl group is connected to the amino group, and the other end of the ethoxy group is connected to a benzyl group containing 2,6-difluoro substitution.
The 4th position of the thiophene ring is connected with dimethylaminomethyl, that is, a methyl group substituted with dimethylamino. The 5th position of the thiophene ring is connected with 4-nitrophenyl, which is the p-position of the phenyl group substituted with nitro. The 3rd position of the thiophene ring is a carboxyl group.
In terms of chemical structure, the thiophene ring is like a central center, and each substituent is connected in an orderly manner, just like the star and the moon, and each position is at an ampere, which together constitutes the unique chemical structure of this organic compound. The complexity of its structure highlights the delicacy of organic chemistry, with atoms and groups connected in a specific way, giving this compound its unique chemical and physical properties.
What is the main use of 2- [2,6-Difluorobenzyl] Ethoxycarbonylamino] -4- [Dimethylaminomethyl] -5-4-Nitrophenylthiophene-3-Carboxylic acid?
2-% 5B2% 2C6-difluorobenzyl% 5D-ethoxycarbonyl amino% 5D-4-% 5B-dimethylaminomethyl% 5D-5-4-nitrobenzene thiothiophene-3-carboxylic acid, this is a rather complex organic compound. At the time of "Tiangong Kaiji", although there were no such fine organic synthesis products, but from an ancient perspective, such compounds may have potential uses in many fields such as medicine and chemical industry.
In the field of medicine, many organic compounds are now key components in drug development. This compound may have a unique chemical structure and properties, which can act on specific targets in the human body to achieve the effect of treating diseases. Just as in the past, physicians studied herbs to explore their active ingredients and pharmacology, today's organic compounds follow this path, and through scientific research, they may be able to find a cure for difficult diseases.
In the chemical industry, such compounds may be used as synthetic raw materials for special materials. In the past, craftsmen used natural materials to produce the desired materials through many processes, and today's organic synthesis is also an important means of chemical industry. This compound can be made into materials with special properties after specific reactions and processing, such as high-strength, corrosion-resistant materials, which are used in equipment manufacturing, construction and other fields.
These are all speculations based on today's knowledge and application. Although "Tiangong Kaiwu" does not contain such compounds, the spirit of research and creativity it shows is in line with today's scientific research. This compound is waiting for scientists to explore in depth in today's world to clarify its exact use and value, and to contribute to human well-being.
What are the synthesis methods of 2- [2,6-Difluorobenzyl] Ethoxycarbonylamino] -4- [Dimethylaminomethyl] -5-4-Nitrophenylthiophene-3-Carboxylic acid?
To prepare 2 - [2,6 - difluorobenzyl] ethoxycarbonylamino - 4 - [dimethylaminomethyl] - 5 - (4 - nitrophenyl) thiophene - 3 - carboxylic acid, the synthesis method is quite complicated. First, find a suitable starting material, using 2,6 - difluorobenzyl alcohol and ethyl chloroformate as groups, through condensation reaction, to obtain 2,6 - difluorobenzyl ethoxycarbonyl chloride. In this step, the temperature and pH of the reaction need to be carefully adjusted to ensure the best yield.
Next, the thiophene-containing compound is used as the substrate to introduce the dimethylaminomethyl group. By means of nucleophilic substitution, the thiophene derivative can be co-heated with the dimethylaminomethylation reagent in a suitable solvent to form a 4- [dimethylaminomethyl] thiophene intermediate. This process requires careful observation of the reaction time and the ratio of the reactants to avoid side reactions.
Furthermore, 4-nitrophenyl is introduced into the 5-position of thiophene. The above intermediate can be coupled with 4-nitrophenyl halide through a palladium-catalyzed coupling reaction. This reaction requires the selection of suitable ligands and bases, and the reaction environment must be anhydrous and oxygen-free to achieve good results.
Finally, a carboxyl group is constructed at the 3-position of thiophene. Or by various means such as hydrolysis and oxidation, the existing functional groups are converted into carboxyl groups. During hydrolysis, the conditions of the reaction need to be controlled to prevent other groups from being affected. During oxidation, suitable oxidants and reaction media need to be selected.
After each step of the reaction, various separation and purification methods, such as column chromatography, recrystallization, etc., are required to obtain a pure product. Thus, the target compound 2 - [2,6 - difluorobenzyl] ethoxycarbonyl amino - 4 - [dimethylaminomethyl] - 5 - (4 - nitrophenyl) thiophene - 3 - carboxylic acid can be obtained by careful operation in several steps.
What are the physical properties of 2- [2,6-Difluorobenzyl] Ethoxycarbonylamino] -4- [Dimethylaminomethyl] -5-4-Nitrophenylthiophene-3-Carboxylic acid?
2-%5B2%2C6-Difluorobenzyl%5DEthoxycarbonylamino%5D-4-%5BDimethylaminomethyl%5D-5-4-Nitrophenylthiophene-3-Carboxylic acid is an organic compound, and its physical properties are as follows:
- ** Appearance **: This compound is usually solid, but its appearance may be slightly different due to differences in preparation methods and purity. Pure or white to pale yellow crystalline powder, under light, or slightly shiny, if it contains impurities, color or slightly darker, appearance or rough.
- ** Melting point **: Melting point is the temperature at which a substance changes from solid to liquid. For this compound, the exact melting point varies depending on experimental conditions and is roughly in a specific temperature range. Measuring the melting point can help to distinguish its purity. Those with high purity have a narrow melting point range; when impurities are included, the melting point decreases and the range becomes wider. < Br > - ** Solubility **: In organic solvents, its solubility varies. In common organic solvents such as dichloromethane and chloroform, or with good solubility, it can be uniformly dispersed to form a solution; in polar solvents such as water and methanol, the solubility is poor, only slightly soluble or insoluble. This difference in solubility is determined by the properties of the groups in its molecular structure. The hydrophobic groups make it insoluble in polar solvents, but have good miscibility with non-polar organic solvents.
- ** Density **: The density reflects the mass of the substance per unit volume, and the density of the compound is also affected by purity and environmental factors. Although the exact value needs to be accurately determined experimentally, it can be speculated that its structure and similar compounds may exhibit different densities compared to water, which is of great significance for its distribution in solution and separation operations.
2- [2,6-Difluorobenzyl] Ethoxycarbonylamino] -4- [Dimethylaminomethyl] -5-4-Nitrophenylthiophene-3-Carboxylic acid What is the price range in the market?
I do not know the price range of 2 - [2,6 - difluorobenzyl] ethoxycarbonylamino - 4 - [dimethylaminomethyl] - 5 - 4 - nitrophenylthiophene - 3 - carboxylic acid in the market. This compound may be a relatively uncommon chemical substance, and the market price often varies depending on quality, purity, supplier and purchase quantity. If it is found in the chemical raw material market, the price may be better when purchasing in bulk; if it is purchased in small quantities, such as for scientific research purposes, the price may be higher due to factors such as preparation difficulty and demand.
To know the exact price range, you can check the chemical trading platform, the supplier's official website, or contact the chemical raw material distributor for consultation. They can provide relatively accurate price information based on current market conditions and demand.