Chemical Formula | C16H20F2NO2 |
Molecular Weight | 295.33 |
Appearance | Solid (predicted) |
Boiling Point | Predicted to be high due to hydrogen - bonding and van der Waals forces |
Melting Point | Depends on crystal structure, likely in a range characteristic for organic amides |
Solubility In Water | Low, due to non - polar phenyl and cyclohexyl groups |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, ethyl acetate |
Polarity | Moderate, due to presence of polar amide and hydroxyl groups |
Chirality | Chiral, due to (1S) - configuration in the side - chain |
Stability | Stable under normal conditions, but can react with strong acids or bases |
Chemical Formula | C16H21F2NO2 |
Molecular Weight | 297.34 |
Physical State | Solid (predicted) |
Appearance | White to off - white powder (predicted) |
Solubility In Water | Low solubility (predicted due to non - polar nature of parts of the molecule) |
Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, dichloromethane (predicted based on structure) |
Logp | Positive value (predicted, indicating lipophilicity) |
Chemical Formula | C19H21F2NO2 |
Molecular Weight | 333.37 |
Appearance | Solid (usually white or off - white powder) |
Physical State At Room Temperature | Solid |
Melting Point | Varies, specific data depends on purity |
Solubility In Water | Low solubility in water |
Solubility In Organic Solvents | Soluble in some organic solvents like ethanol, dichloromethane |
Odor | Odorless or very faint odor |
Stability | Stable under normal storage conditions away from strong oxidizing agents |
Chemical Name | 4,4-Difluoro-N-[(1S)-3-hydroxy-1-phenylpropyl]cyclohexanecarboxamide |
Molecular Formula | C16H21F2NO2 |
Molecular Weight | 297.34 |
Appearance | Solid (usually) |
Physical State At Room Temp | Solid |
Melting Point | Varies, specific value depends on purity and measurement method |
Solubility In Water | Low solubility |
Solubility In Organic Solvents | Soluble in some organic solvents like dichloromethane, ethanol to some extent |
Logp | Estimated to be relatively lipophilic due to aromatic and cyclohexyl groups |
What is the chemical structure of 4,4-difluoro-N- [ (1S) -3-hydroxy-1-phenylpropyl] cyclohexane formamide
4,4-diene-N- [ (1S) -3-methoxy-1-phenylethyl] cyclohexanecarbonamide is one of the organic compounds. To clarify its chemical structure, it is necessary to analyze the key information contained in its naming.
"4,4-diene" indicates that there are two carbon-carbon double bonds at the 4th carbon atom on the main chain of the compound. The existence of this double bond gives the compound a specific chemical activity and spatial configuration.
"Cyclohexanecarbonamide" indicates that the basic structure of the main chain is a cyclohexane ring, and the ring is connected to a formamide group. The cyclohexane ring provides a rigid ring structure, while the formamide group contains carbonyl and amino groups, which can participate in various chemical reactions, such as the formation of hydrogen bonds, and have a great influence on the physical and chemical properties of compounds.
"N - [ (1S) -3 -methoxy-1 -phenylethyl]" represents the substituent attached to the nitrogen atom of formamide. This substituent has a specific three-dimensional configuration (1S), which contains a methoxy group and a phenyl group, which are connected to the ethyl group. The oxygen atom of the methoxy group has lone pairs of electrons, which can affect the polarity and electron cloud distribution of the molecule; the conjugated structure of the phenyl group makes the molecule have certain stability and hydrophobicity.
In general, the chemical structure of 4,4-diene-N- [ (1S) -3-methoxy-1-phenylethyl] cyclohexanecarbonamide consists of a double-bonded cyclohexane ring, a formamide group, and a substituent of a specific configuration. The interaction of each part jointly determines the unique properties and reactivity of the compound.
What are the main uses of 4,4-difluoro-N- [ (1S) -3-hydroxy-1-phenylpropyl] cyclohexane formamide
4,4-Diene-N- [ (1S) -3 -methoxy-1-naphthyl ethyl] cyclohexanecarbonamide is a rather complex organic compound. Its main uses are mostly in the following fields:
First, in the process of pharmaceutical research and development, it may be used as a potential active ingredient. Cover organic compounds often have unique chemical structures and activities, or can be combined with specific targets in organisms, such as receptors, enzymes, etc. From the perspective of modern pharmacological research, it may regulate physiological processes, play a therapeutic effect on specific diseases, such as inflammation, tumors and other diseases, or show inhibitory and alleviating functions.
Second, in the field of organic synthesis, it can be a key intermediate. Organic synthesis aims to build more complex compounds with specific functions. With its unique structure, it can be derived through a series of chemical reactions, such as substitution, addition, oxidation and reduction, etc. Novel compounds can be derived, expanding the types and application fields of organic compounds, paving the way for the development of materials science, medicinal chemistry and other disciplines.
Third, in the field of chemical research, in-depth exploration of its structure and properties can contribute to the improvement of chemical theory. Studying their physical and chemical properties, such as melting point, boiling point, solubility, etc., as well as chemical properties, such as reactivity and selectivity, helps chemists to more accurately grasp the behavior of organic compounds and provide theoretical support for the development of new reactions and methods.
What is the synthesis method of 4,4-difluoro-N- [ (1S) -3-hydroxy-1-phenylpropyl] cyclohexane formamide
The synthesis of 4,4-diene-N- [ (1S) -3-methoxy-1-phenylethyl] cyclohexanecarbonamide is a key problem in the field of organic synthesis. This compound has a unique structure and contains multiple functional groups, and the synthesis requires delicate design steps.
The first consideration should be the selection of starting materials. Compounds with suitable activity and structure should be selected to lay the foundation for subsequent reactions. Or compounds containing benzene rings and alkenyl groups can be selected, and methoxy groups and cyclohexanecarbonamide groups can be modified to introduce.
The starting material is established, and a series of reactions need to be planned. Or the nucleophilic substitution reaction can be used to introduce the methoxy group at the appropriate position of the benzene ring. This step should be carefully selected to ensure the accurate substitution check point.
Then, the reaction involving alkenyl groups, such as olefin metathesis reaction, can be used to construct the 4,4-diene structure. This reaction requires a suitable catalyst and reaction environment to promote the correct formation and configuration maintenance of double bonds.
Carbon-nitrogen bonds are constructed to introduce the N - [ (1S) -3 -methoxy-1 -phenylethyl] moiety, or amidation reactions can be used. Here, it is necessary to activate the carboxylic acid or amine group, select a suitable condensing agent, so that the two can react efficiently, and pay attention to stereochemical control to obtain the target configuration product.
In the synthesis process, the products of each step of the reaction need to be separated and purified, such as column chromatography, recrystallization and other means to remove impurities and ensure the smooth progress of the reaction.
The reaction conditions are also crucial, and the temperature, solvent, reaction time, etc. need to be carefully regulated. Each step of the reaction needs to be carried out under suitable conditions to obtain the product with ideal yield and purity.
Synthesis of 4,4-diene-N- [ (1S) -3-methoxy-1-phenylethyl] cyclohexanecarbonamide requires clever design of reaction routes, precise control of reaction conditions, and careful handling of each step of the reaction product, in order to achieve the goal.
What are the physical properties of 4,4-difluoro-N- [ (1S) -3-hydroxy-1-phenylpropyl] cyclohexane formamide
4,4-Diene-N- [ (1S) -3-methoxy-1-naphthyl ethyl] cyclohexanecarbonamide is an organic compound with unique physical properties. Its properties are often in the state of a crystalline solid. Due to the intermolecular force, it forms a regular lattice structure and has good stability.
When it comes to the melting point, it is usually within a certain range. This value is crucial for the identification and purification of this compound. Due to the specific lattice energy endowed by the molecular structure, melting requires a certain amount of heat to overcome lattice binding. The specific melting point reflects its molecular structure and purity.
In terms of solubility, it varies in organic solvents. In polar organic solvents, such as ethanol and acetone, or with a certain solubility, polar molecules can form interaction forces with some groups of the compound, such as hydrogen bonds, dipole-dipole interactions, etc., which help them disperse in solvents. However, in non-polar organic solvents, such as n-hexane, the solubility may be limited due to the large difference between molecular polarity and non-polar solvents, and the interaction force is weak.
In addition, the density of the compound is also one of its physical properties. The density depends on the molecular mass and the way of molecular accumulation, which has an important impact on its application in specific environments, such as distribution in mixed systems.
Furthermore, its appearance may be white to off-white, which is related to the light absorption and scattering characteristics of the molecule. The specific structure makes the absorbed and scattered light exhibit such color characteristics in the visible range, which is one of the visual identification criteria.
What is the market outlook for 4,4-difluoro-N- [ (1S) -3-hydroxy-1-phenylpropyl] cyclohexane formamide?
4,4-Diene-N- [ (1S) -3-cyano-1-phenylethyl] cyclohexanecarbonamide is quite promising in terms of market prospects. In today's world, the field of pharmaceutical and chemical industry is booming, and many innovative drugs have been developed one after another. Due to their unique chemical structure and potential biological activity, these compounds can be used as key intermediates in the process of drug creation.
Looking at the current pharmaceutical market, there is a hunger for new drugs against various diseases. 4,4-diene-N- [ (1S) -3-cyano-1-phenylethyl] cyclohexanecarbonamide may play an indispensable role in the development of therapeutic drugs for certain diseases. Taking anti-tumor drugs as an example, their structural properties may open up a new path for drug molecular design, making the developed new drugs more targeted and inhibitory to tumor cells, thus bringing good news to the majority of patients.
Furthermore, with the increasingly sophisticated organic synthesis technology, the preparation process of this compound is also gradually maturing. More efficient and green synthesis methods continue to emerge, which not only reduce production costs, but also improve product quality and yield. In this way, it lays a solid foundation for its large-scale market entry.
In the fields of materials science and other fields, this compound may also have potential applications. Its special structure may endow materials with novel physical and chemical properties, such as improved material stability and optical properties. It can be seen that 4,4-diene-N- [ (1S) -3-cyano-1-phenylethyl] cyclohexanecarbonamide has broad market prospects in the future, and is expected to shine in many fields and lead new changes in the industry.