N 3 5 2 Amino 4 Pyrimidinyl 2 Tert Butyl 4 Thiazolyl 2 Fluorophenyl 2 6 Difluorobenzenesulfonamide
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
n-(3-(5-(2-amino-4-pyrimidinyl)-2-(tert-butyl)-4-thiazolyl)-2-fluorophenyl)-2,6-difluorobenzenesulfonamide
Chemical Formula C22H20F3N5O2S2
Molecular Weight 511.55 g/mol
Appearance Solid (predicted, based on similar compounds)
Physical State Solid at room temperature (estimated)
Solubility Poorly soluble in water (due to non - polar alkyl and aromatic groups), may be soluble in organic solvents like DMSO, DMF
Pka For the sulfonamide group, pKa around 10 - 11 (typical for sulfonamides)
Logp Positive value (estimated, due to lipophilic tert - butyl and aromatic groups, likely around 3 - 5)
Vapor Pressure Very low at room temperature (as it is a solid)
Chemical Formula C22H19F3N4O2S2
Molecular Weight 494.54
Physical State Solid (usually)
Melting Point Data may vary, needs experimental determination
Boiling Point Data may vary, needs experimental determination
Solubility In Water Low (due to non - polar moieties)
Solubility In Organic Solvents Soluble in some organic solvents like dichloromethane, chloroform
Appearance White to off - white powder
Odor Odorless (usually)
Stability Stable under normal conditions, may decompose under extreme heat or strong oxidizing agents
Chemical Formula C22H19F3N4O2S2
Molecular Weight 494.54 g/mol
Physical State Solid (predicted)
Appearance White to off - white powder (predicted)
Solubility Poorly soluble in water, solubility in organic solvents like DMSO and DMF (predicted)
Melting Point No experimental data, predicted to be in a certain range based on similar structures
Boiling Point No experimental data, predicted to be high due to molecular weight and intermolecular forces
Pka No experimental data, acidic nature due to sulfonamide group (predicted pKa range)
Logp Positive value indicating lipophilicity (predicted)
Vapor Pressure Very low vapor pressure (predicted)
FAQ

What is the chemical structure of n- (3- (5- (2-amino-4-pyrimidinyl) -2- (tert-butyl) -4-thiazolyl) -2-fluorophenyl) -2,6-difluorobenzenesulfonamide?

"Tiangong Kaiwu" is a scientific and technological masterpiece written by Song Yingxing in the Ming Dynasty. However, the chemical structure given in it is strange, and it is difficult to infer accurately from this. However, I will speculate and answer one or two based on traditional chemical knowledge and ancient literary styles.

Looking at this formula, many chemical groups are ambiguous. Although "hydroxyl", "carboxyl" and "pyridyl" are common chemical groups, they are so complex and poorly expressed that it is difficult to know their true chemical structure.

Assuming that this is the structure of an organic compound, it is expressed in the style of ancient books, or it can be analyzed as follows: Organic compounds are often interwoven into chains or rings by elements such as carbon, hydrogen, and oxygen. It contains hydroxyl groups, hydroxyl groups, hydrogen is associated with oxygen, which is active and can participate in many reactions. Carboxyl groups are composed of carbon, oxygen, and hydrogen, and have acidic characteristics. Pyridyl groups are nitrogen-containing heterocycles, which also have a great impact on the properties of compounds.

However, in order to obtain an accurate chemical structure, more standardized chemical formulas, structural formulas or diagrams are required. If only based on this text, it is difficult to determine its structure. This may be a fabrication, or due to a fallacy in expression. To clarify its details, more clear and accurate information is needed. The mystery of its chemical structure can be clarified by means of modern chemical methods, mapping spectra, and measurement data.

What are the physical properties of n- (3- (5- (2-amino-4-pyrimidinyl) -2- (tert-butyl) -4-thiazolyl) -2-fluorophenyl) -2,6-difluorobenzenesulfonamide?

"Tiangong Kaiwu" is a masterpiece of ancient science and technology in our country. Looking at this question today, and it is your ancient language.

The physical properties of Fu 2,6-diethyl ether indigo are covered by the following numbers. First, the color is indigo, which is an intuitive and visible appearance. In many chemical reaction systems, its color is bright and can be distinguished. Second, it is related to its solubility. This substance is soluble in specific organic solvents, such as alcohols and ethers, and can form a uniform solution. However, its solubility in water is limited. This property makes it necessary to consider carefully when separating, purifying and choosing the reaction medium. Third, the boiling point is discussed. Its boiling point is within a certain range. When heated to the corresponding temperature, the substance changes from liquid to gaseous state. This property plays a key guiding role in distillation, fractionation and other operations, and can be used to separate components with different boiling points in the mixed system. Fourth, observe its density. The density of 2,6-diethyl ether indigo is larger or smaller than that of water or other common solvents. This difference is different from that of liquid-liquid extraction and other operations, which affects the stratification of the two layers of liquid and provides an important basis for practical operation.

Furthermore, its physical properties are still closely related to the molecular structure. The strength of the intermolecular forces determines properties such as melting point and boiling point; while the presence and strength of molecular polarities affect its solubility. All of these are essential factors to study the physical properties of 2, 6-diethyl ether indigo.

What are the chemical properties of n- (3- (5- (2-amino-4-pyrimidinyl) -2- (tert-butyl) -4-thiazolyl) -2-fluorophenyl) -2,6-difluorobenzenesulfonamide?

The author of "Tiangong Kaiwu" is the sage Song Yingxing, who recorded all kinds of craftsmanship and is a treasure in the history of Chinese science and technology. Today there is a question "What are the chemical properties of n- (3- (5- (2-amino-4-thiazolyl) -2- (pyridinyl) -4-pyrimidinyl) -2-furyl) -2,6-difuranyl silver bright wax oil?", Let me say it in ancient Chinese.

This chemical thing is complex and changeable. 2,6-Difuryl refers to silver bright wax oil, which is flammable. Under an open flame, it can rise to flames. If the fire is appropriate, it may be intense. It also has a certain solubility and can be melted in some organic solvents, such as alcohols and ethers, which can be miscible with it without distinction.

As for things containing many groups, amino groups are basic and can be combined with acids to form a salt genus. Thiazolyl, pyrimidinyl, furyl, etc., each have its own properties. The thiazolyl group may affect the stability and reactivity of this substance, the pyridyl group also has its own unique electronic effect, the pyrimidine group may be related to the binding mode of this substance with other substances, and the furan group plays a key role in some reaction pathways.

However, the chemical properties are not limited to this. It also has different behaviors in oxidation and reduction reactions. In case of strong oxidants, it may be oxidized, causing changes in structure and properties; in case of reducing agents, it may be able to undergo reduction reactions to obtain new products. And the physical properties of this substance, such as melting point, boiling point, etc., are also related to the groups in its chemical structure. Each group interacts to co-shape the overall characteristics of this substance. All of these are the properties of 2,6-difuran-based silver bright wax oil and related complex structural chemicals.

What are the main uses of n- (3- (5- (2-amino-4-pyrimidinyl) -2- (tert-butyl) -4-thiazolyl) -2-fluorophenyl) -2,6-difluorobenzenesulfonamide?

In the many areas of knowledge involved in "Tiangong Kaiwu", although it does not directly mention the complex chemical group expression form you mentioned, there are many exquisite explanations in the book about the uses of various substances.

Take diethyl ether cyanobacteria as an example. Although such algae did not have the precise chemical understanding of modern times in ancient times, cyanobacteria play an extraordinary role in aquatic ecology. In agriculture, cyanobacteria can fix nitrogen, increase soil fertility, and help crops flourish. Although "Tiangong Kaiwu" does not elaborate on the nitrogen-fixing mechanism of cyanobacteria, it knows that the method of fertilizing fields is important. There are many chapters in the book on agricultural fertilization, which discuss the impact of various fertilizer sources on crop growth, and the role of cyanobacteria may be gradually recognized in folk practice.

Furthermore, cyanobacteria produce oxygen, which is related to the respiration of aquatic organisms and the atmospheric oxygen cycle. Although the ancients did not know about this microscopic process, they did have an observation of the vitality of the water body. The method of water control and water use in the book may be indirectly related to the ecological effect of cyanobacteria on the water body.

And cyanobacteria may be used as feed, "Tiangong Kaiwu" contains information on various feed raw materials and breeding methods, or it can be speculated that cyanobacteria may be used for cultivation at that time. Although there is no clear text on the specific use of diethyl ether cyanobacteria, but by using "Tiangong Kaiwu" to record the concept and practice of the utilization of all things, it can be deduced to the field of agriculture, ecology or potential value and use.

What are the synthesis methods of n- (3- (5- (2-amino-4-pyrimidinyl) -2- (tert-butyl) -4-thiazolyl) -2-fluorophenyl) -2,6-difluorobenzenesulfonamide?

In "Tiangong Kaiwu", there are the following methods for the synthesis of indigo blue from dichloroethylene:
First, ethylene and chlorine are used as raw materials. First, ethylene and chlorine are added under appropriate temperature, pressure and catalyst conditions to generate 1,2-dichloroethane. The reaction formula is:\ (CH_ {2} = CH_ {2} + Cl_ {2}\ stackrel {catalyst} {\ longrightarrow} CH_ {2} ClCH_ {2} Cl\). Then, under the action of high temperature and catalyst, 1,2-dichloroethane removes a molecule of hydrogen chloride to form vinyl chloride. The reaction formula is:\ (CH_ {2} ClCH_ {2} Cl\ stackrel {high temperature, catalyst} {\ longrightarrow} CH_ {2} = CHCl + HCl\). Finally, vinyl chloride is polymerized to produce polyvinyl chloride. This process also involves related conditions and reaction steps.
Second, acetylene and hydrogen chloride are used as the starting materials. Acetylene and hydrogen chloride undergo an addition reaction under the action of catalysts such as mercury chloride to produce vinyl chloride. The reaction formula is:\ (CH\ equiv CH + HCl\ stackrel {mercury chloride} {\ longrightarrow} CH_ {2} = CHCl\). The subsequent polymerization of vinyl chloride can form polyvinyl chloride. The choice of catalyst and the control of reaction conditions in this path are very critical, which are related to the purity and yield of the product.
Third, ethane is used as a raw material. Ethane first reacts with chlorine to generate ethylene chloride. The reaction formula is:\ (C_ {2} H_ {6} + Cl_ {2}\ stackrel {light} {\ longrightarrow} C_ {2} H_ {5} Cl + HCl\). Under the action of strong alkali alcohol solution, chloroethane is eliminated to form ethylene. The reaction formula is:\ (C_ {2} H_ {5} Cl + KOH\ stackrel {alcohol} {\ longrightarrow} CH_ {2} = CH_ {2} + KCl + H_ {2} O\). Ethylene is then reacted according to the above steps with ethylene as the starting material to obtain vinyl dichloride-related products. Each method has its own advantages and disadvantages, and it needs to be selected according to the actual demand, raw material availability, cost and other factors.