Sodium 2 N 3 5 Difluorophenyl Carbamoylamino C Methylcarbonimidoyl Pyridine 3 Carboxylate
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
sodium 2-[N-[(3,5-difluorophenyl)carbamoylamino]-C-methylcarbonimidoyl]pyridine-3-carboxylate
Chemical Name sodium 2-[N-[(3,5-difluorophenyl)carbamoylamino]-C-methylcarbonimidoyl]pyridine-3-carboxylate
Chemical Formula C16H12F2N3NaO3
Molecular Weight 355.27
Appearance Solid (usually white or off - white powder)
Solubility In Water Moderate solubility, depending on pH
Solubility In Organic Solvents Soluble in some polar organic solvents like DMSO
Melting Point Specific value would require experimental determination
Pka Value Related to the acidic and basic groups in the molecule
Logp Indication of lipophilicity, value needs experimental determination
Stability Stable under normal storage conditions, may degrade under extreme conditions
Ir Spectrum Characteristic absorption bands for functional groups like carbonyl, amide, etc.
Chemical Formula C16H13F2N3NaO3
Molecular Weight 369.28
Appearance Solid (Typical description, actual may vary)
Solubility In Water Limited (Based on general nature of such compounds, exact value may need experimental determination)
Solubility In Organic Solvents Soluble in some polar organic solvents like DMSO (Common behavior, specific solvents and solubility values may vary)
Melting Point Needs experimental determination
Pka Relevant acidic/basic groups' pKa values would depend on the specific structure details and need experimental determination
Logp Can be estimated based on structure, but exact value requires experimental determination
Stability Stable under normal conditions, but may decompose under extreme heat, light or in the presence of certain reactive substances
Chemical Formula C16H13F2N4NaO3
Molecular Weight 386.29
Appearance Solid (Typical description, actual may vary)
Solubility In Water Limited (Typical for such compounds, actual needs precise measurement)
Solubility In Organic Solvents Soluble in some organic solvents like dichloromethane (Typical, actual may vary)
Melting Point Data required from experimental determination
Boiling Point Data required from experimental determination
Pka Value Data required from experimental determination
Ph In Solution Data required from experimental determination
Stability Stable under normal conditions (Typical, subject to experimental verification)
Chemical Name sodium 2-[N-[(3,5-difluorophenyl)carbamoylamino]-C-methylcarbonimidoyl]pyridine-3-carboxylate
FAQ

What is the chemical structure of sodium 2- [N- [ (3,5-difluorophenyl) carbamoylamino] -C-methylcarbonimidoyl] pyridine-3-carboxylate

This is the chemical name of an organic compound. In order to know its chemical structure, it is necessary to analyze the meanings of each part of this name. "Sodium" is sodium, indicating that the compound is a sodium salt. In "2 - [N - [ (3,5 - difluorophenyl) carbamido] -C - methylcarbodiimide] pyridine-3 - carboxylate", pyridine-3 - carboxylate is the basic structure, and the pyridine ring is a six-membered nitrogen-containing heterocycle with a 3-position linked carboxylate group. A complex side chain is connected to the second position of pyridine, and the N atom in the side chain is connected with (3,5-difluorophenyl) carbamide, that is, 3,5-difluorophenyl is connected to the carbamide group and then connected to the N atom; C-methyl carbamide is a carbon-nitrogen double bond and a methyl structure. In general, the chemical structure of this compound is based on pyridine-3-carboxylate as the core, and the 2-position side chain contains specific substituents. Its structure is complex, and it is cleverly combined with a variety of functional groups, presenting unique chemical properties.

What are the main uses of sodium 2- [N- [ (3,5-difluorophenyl) carbamoylamino] -C-methylcarbonimidoyl] pyridine-3-carboxylate

Sodium-2 - [N - [ (3,5 -difluorophenyl) carbamido] -C -methylcarbodiimido] pyridine-3 -carboxylate, this compound is widely used in the field of medicinal chemistry.

First, it may be a key intermediate in the journey of drug development. Just like the cornerstone of building a magnificent building, this compound can be used as a starting material, and through many delicate chemical reactions, complex structures and specific biological activities can be constructed. Drug molecules with specific biological activities. For example, by partially modifying its pyridine and difluorophenyl, the affinity of the drug with specific targets can be adjusted, which is like a key to lock in the exclusive key, improve the efficacy and specificity of the drug, or is expected to lead to innovative drugs for the treatment of specific diseases.

Second, in the field of biological activity research, this compound itself may have unique biological activities. Like a warrior holding a sword, it may directly act on specific targets in organisms, such as enzymes, receptors, etc. After binding to receptors, it may regulate cell signaling pathways and affect key physiological processes such as cell growth, differentiation and apoptosis. Therefore, in-depth exploration of its biological activities may reveal new drug action mechanisms and open up new avenues for disease treatment strategies.

Third, in the field of materials science, it has also emerged. If it has specific optical, electrical or thermal properties, it can be applied to the creation of new functional materials. It is like finding special materials, providing the possibility for the manufacture of high-performance sensors, luminescent materials and other materials, injecting new vitality into the development of materials science.

What is the synthesis method of sodium 2- [N- [ (3,5-difluorophenyl) carbamoylamino] -C-methylcarbonimidoyl] pyridine-3-carboxylate

To prepare the sodium+2-%5BN-%5B%283%2C5-difluorophenyl%29carbamoylamino%5D-C-methylcarbonimidoyl%5Dpyridine-3-carboxylate, the method is as follows:

First take the pyridine-3-carboxylic acid as the group, and react with appropriate reagents by acylation to obtain the acylation of the pyridine-3-carboxylic acid. In this acylate, an amine containing a specific substituent is introduced, and the amine contains a carbamide group of 3,5-difluorophenyl, so that the two condensation reactions occur. This reaction requires the selection of a suitable solvent, such as an aprotic organic solvent, and temperature control and pH adjustment to make the reaction smooth.

At the same time, another reagent containing C-methylcarbodiimide is prepared, which further reacts with the obtained product. This step also requires careful control of its conditions, such as temperature, reactant ratio, etc.

After the reaction is completed, impurities are removed through separation and purification techniques, such as column chromatography, recrystallization, etc., and the final product is sodium+2-%5BN-%5B%283%2C5-difluorophenyl%29carbamoylamino%5D-C-methylcarbonimidoyl%5Dpyridine-3-carboxylate. The whole process requires strict adherence to experimental procedures and precise operation to ensure the purity and yield of the product.

What are the physicochemical properties of sodium 2- [N- [ (3,5-difluorophenyl) carbamoylamino] -C-methylcarbonimidoyl] pyridine-3-carboxylate

This is a chemical substance named "2 - [N- [ (3,5 - difluorophenyl) carbamido] -C - methylcarbodiimide] pyridine-3 - sodium carboxylate". Its physical and chemical properties are as follows:
In terms of view, it may be a white to off-white solid, which is a common color state of many organic carboxylate compounds. In terms of solubility, because of its sodium carboxylate structure, it may have certain solubility in water. Carboxylate salts have this property and can be dissolved with water molecules by ion-dipole interaction. In organic solvents, the solubility may vary depending on the type of solvent, such as in polar organic solvents such as methanol and ethanol, the solubility may be better than that of non-polar solvents such as n-hexane.
When it comes to stability, the structures of pyridine rings, amino groups, carboxylic salts, etc. in this compound are relatively stable under general circumstances. In case of strong acids, the sodium carboxylate part may be converted to carboxylic acids; in case of strong bases, some chemical bonds in the molecule may be destroyed due to reactions such as nucleophilic substitution. In high temperature environments, molecular decomposition or rearrangement reactions may also be triggered.
Its melting point, although the exact value needs to be determined experimentally, is estimated to be not low due to the interaction of hydrogen bonds and van der Waals forces between molecules. The molecule contains fluorine atoms, which have a large electronegativity, which has an impact on molecular polarity, stability and biological activity, or makes the compound have unique physical and chemical properties. Conjugated systems containing multiple conjugated structures, such as pyridine rings and benzene rings, may have specific absorption peaks in UV-visible spectrum, which can be used for qualitative and quantitative analysis.

Sodium 2- [N- [ (3,5-difluorophenyl) carbamoylamino] -C-methylcarbonimidoyl] pyridine-3-carboxylate prospects in the market

Guanfu sodium + 2 - [N- [ (3,5 -difluorophenyl) carbamido] -C -methylcarbodiimino] pyridine-3 -carboxylate This compound needs to be explored in detail in the future of the market.

In terms of its characteristics, the structure of this compound is unique. 3,5-difluorophenyl, carbamido and carbamido are partially connected to each other, giving it specific chemical activity. However, in the market, the display of characteristics depends on whether it can meet diverse needs. If its chemical activity can be precisely regulated, it may find opportunities in the fields of medicine and chemical industry.

In the field of medicine, current pharmaceutical research and development strives to be efficient and targeted drugs. If this compound has affinity for specific biological targets, it can participate in precise biochemical reactions, or it can be developed into a new type of drug. If it can fight some difficult diseases, if it can interfere with the metabolic pathway of pathogens with its unique structure and block their reproduction, it will be a great help for the pharmaceutical industry, and the prospect should be broad.

In the field of chemical industry, it is also promising. Due to its special structure, it can be used as an efficient catalyst to accelerate the process of specific chemical reactions; or it can be used as an additive with excellent performance to improve the physical and chemical properties of materials, such as enhancing the stability and flexibility of polymers. If this can be done, it will make a great contribution to the upgrading and replacement of chemical products, and the market prospect will also expand accordingly.

However, its prospects are not without worries. The difficulty and cost of synthesis are all key. If the synthesis process is complicated and expensive, even if the performance is excellent, it is difficult to promote on a large scale. Furthermore, the market competition is fierce, and congeneric products or potential substitutes emerge one after another. If you can't stand out in terms of performance, price, environmental protection, etc., it may be difficult to gain a firm foothold in the market.

In summary, sodium + 2- [N- [ (3,5 -difluorophenyl) carbamido] -C -methylcarbodiimide] pyridine-3 -carboxylate in the market prospects, opportunities and challenges coexist. If we can overcome the synthesis problem, highlight the performance advantages, and properly deal with the competition, we will be able to gain a place in the market and shine.