Chemical Formula | C13H19NO |
Molar Mass | 205.296 g/mol |
Appearance | Typically a solid |
Physical State At Room Temperature | Solid |
Melting Point | Data may vary |
Boiling Point | Data may vary |
Solubility In Water | Low solubility |
Solubility In Organic Solvents | Soluble in some organic solvents |
Odor | Specific odor, data may vary |
Density | Data may vary |
Vapor Pressure | Low vapor pressure |
Stability | Stable under normal conditions |
Flash Point | Data may vary |
Hazardous Nature | May have certain hazards, specific data required |
What are the chemical properties of 7-Methoxy-2,2,4-Trimethyl-1,2-Dihydroquinoline?
7-Methoxy-2,2,4-trimethyl-1,2-dihydroquinoline, this is an organic compound. Its chemical properties are unique and of great research value.
Looking at its structure, it contains methoxy, methyl and other groups. Methoxy is a power supply group, which has a great influence on the electron cloud distribution of compounds and can cause changes in their reactivity. In many chemical reactions, methoxy groups often participate in nucleophilic substitution, electrophilic substitution and other processes. The presence of methyl groups also has a significant effect on the properties of compounds. The introduction of multiple methyl groups increases the steric resistance of molecules, making the molecular configuration more stable, and at the same time affects the physical properties such as solubility and boiling point of compounds.
As far as reactivity is concerned, because the molecular structure contains double bonds and aromatic ring parts, addition reactions and substitution reactions on aromatic rings can occur. Double bonds can be added to electrophilic reagents, such as hydrogen halides, halogens, etc., to generate corresponding addition products. In the aromatic ring part, due to the methoxy group electron conductor effect, the density of adjacent and para-position electron clouds increases, and electrophilic substitution reactions are more likely to occur, such as halogenation, nitrification, sulfonation, etc.
Furthermore, the presence of nitrogen atoms in this compound endows the molecule with a certain alkalinity. Although the nitrogen atom in the dihydroquinoline structure is less basic than that of aliphatic amines, it can still form salts with acids under suitable conditions. This property is of great significance in the fields of medicinal chemistry and organic synthesis.
In terms of stability, the aromatic ring structure in the molecule endows it with certain thermal and chemical stability. However, due to the existence of double bonds, oxidation, polymerization and other reactions can still occur under extreme conditions such as strong oxidants and high temperatures, resulting in structural damage.
The chemical properties of 7-methoxy-2,2,4-trimethyl-1,2-dihydroquinoline are determined by its unique structure, and have broad application prospects in organic synthesis, drug research and development, etc. Researchers can rationally design reactions and prepare desired compounds according to their properties.
What are the main uses of 7-Methoxy-2,2,4-Trimethyl-1,2-Dihydroquinoline?
7-Methoxy-2,2,4-trimethyl-1,2-dihydroquinoline has a wide range of uses. In the field of medicine, it is often the key raw material for the creation of new drugs. Due to the unique chemical structure of the compound, it is endowed with specific biological activities, can interact with human biomolecules, or can regulate physiological processes, and then pave the way for the treatment of diseases.
In the field of materials science, this compound also has extraordinary performance. Or can participate in the synthesis of materials with special properties, such as smart materials that respond to specific light, temperature, chemical substances and other stimuli. Its structural characteristics make the prepared materials have unique optical, electrical or mechanical properties, which can be applied to optoelectronic devices, sensors and many other aspects.
Furthermore, in the field of organic synthesis, 7-methoxy-2,2,4-trimethyl-1,2-dihydroquinoline can be regarded as an important intermediate. Organic chemists can modify and transform its structure to construct more complex and diverse organic compounds, expand the boundaries of organic synthesis, and provide possibilities for the development of novel functional materials, drugs and fine chemicals.
In addition, in some special fields, such as the fragrance industry, it may also have potential applications. Due to its unique chemical structure, it may endow fragrances with unique aroma characteristics, providing new options for blending novel and fascinating fragrances. In conclusion, 7-methoxy-2,2,4-trimethyl-1,2-dihydroquinoline has important value in many fields, promoting innovation and development in various fields.
What is the synthesis method of 7-Methoxy-2,2,4-Trimethyl-1,2-Dihydroquinoline?
The synthesis method of 7-methoxy-2,2,4-trimethyl-1,2-dihydroquinoline is an important topic in organic synthesis chemistry. There are several ways to synthesize it.
First, it can be started from an appropriate aromatic compound. First, take a phenolic compound with a specific substituent and make it with a specific olefin derivative under the action of a suitable catalyst. This catalyst is often selected Lewis acids, such as aluminum trichloride. After this reaction, a preliminary intermediate can be formed. The structure of the intermediate needs to be confirmed by precise analytical methods, such as nuclear magnetic resonance and mass spectrometry. < Br >
Then, the intermediate is cyclized under specific reaction conditions. During the cyclization process, the temperature, solvent and other factors of the reaction may need to be adjusted. The temperature may be controlled in a moderate range, such as between 100 and 150 ° C. The solvent can be selected with a high boiling point and suitable polarity, such as N, N-dimethylformamide. After cyclization, the product containing quinoline mother nucleus can be preliminarily obtained.
However, this product has not yet reached the requirements of the target product in terms of the substitution position and quantity of methoxy and methyl groups. Therefore, further modification is required. The halogenation reaction can be used to introduce halogen atoms at suitable positions, and then a metal-organic reagent, such as Grignard reagent, can perform a nucleophilic substitution reaction to introduce methyl groups. The introduction of methoxy groups can be achieved by the nucleophilic substitution reaction of phenolic compounds and halogenated methane under basic conditions.
Another method can be started from the heterocyclic precursor containing nitrogen. First, a pyridine derivative with a suitable substituent is prepared, and the pyridine ring is partially reduced to a dihydropyridine structure through a reduction reaction. For this reduction reaction, a metal hydride reducer such as sodium borohydride can be selected. Then, the structure of the target molecule is gradually constructed by nucleophilic substitution reaction with methoxy and methyl reagents, such as methoxy halogenated hydrocarbons, methyl halogenated hydrocarbons, etc. under alkali catalysis.
During the synthesis process, the products of each step of the reaction need to be strictly separated and purified. Commonly used methods include column chromatography, recrystallization, etc. With precise synthesis steps and strict purification methods, 7-methoxy-2,2,4-trimethyl-1,2-dihydroquinoline can be effectively obtained.
What is the market outlook for 7-Methoxy-2,2,4-Trimethyl-1,2-Dihydroquinoline?
7-Methoxy-2,2,4-trimethyl-1,2-dihydroquinoline, how is the situation in the city? This is a compound in the field of fine chemicals. Although not widely used, it is also important in specific fields.
Looking at its market conditions, I will give you a statement first. Its preparation requires specific technologies and processes, so there are not many producers. Manufacturers are mostly those with profound chemical technology, and the output varies according to the technical level and production capacity. It is difficult to obtain raw materials and control the production process, so the supply is not in a state of flooding, but relatively stable and limited.
Let's discuss again. In pharmaceutical research and development, or as a key intermediate, due to its special structure, it can assist in the synthesis of compounds with specific pharmacological activities. In the field of materials science, or involved in the preparation of light and electricity-related functional materials, with its structural properties, it adds special properties to the material. However, there are many research and exploration stages for these applications, so the demand has not increased sharply for the time being, mainly in specific scientific research institutions, pharmaceutical companies and material research and development enterprises.
Therefore, the market of 7-methoxy-2,2,4-trimethyl-1,2-dihydroquinoline is currently limited, and the demand is niche and concentrated in specific research and development fields. Its market development depends on technological breakthroughs and industrial advancements in medicine, materials and other related fields. If there is a significant increase in research and development, demand may increase, and supply will also expand accordingly, but it is still relatively stable and has potential to be tapped.
What are the precautions for 7-Methoxy-2,2,4-Trimethyl-1,2-Dihydroquinoline during storage and transportation?
7-Methoxy-2,2,4-trimethyl-1,2-dihydroquinoline is an organic compound. During storage and transportation, many matters need to be paid attention to.
When storing it, the first environment should be selected. It should be placed in a cool, dry and well-ventilated place. Because the temperature is too high, it is easy to change the properties of this compound or cause chemical reactions; and humid environment, or the compound is damp and deteriorated, affecting its quality. And well-ventilated, it can disperse harmful gases that may be generated in time to ensure safe storage.
In addition, storage containers should also be carefully selected. Containers with good sealing performance should be used to prevent the compound from contacting with air. Due to the oxygen, moisture and other components in the air, or reactions with the compound such as oxidation. It is also crucial to choose a container of suitable material. It is necessary to ensure that the material of the container does not chemically react with 7-methoxy-2,2,4-trimethyl-1,2-dihydroquinoline, so as not to damage the compound or cause corrosion of the container.
As for the transportation process, the relevant regulations and standards must be strictly followed. Before transportation, it is necessary to properly pack the compound to ensure that the package is strong and can withstand the bumps and vibrations during transportation to prevent the leakage of the compound due to package damage. The transportation vehicle should also have suitable conditions, such as temperature control devices, to maintain a suitable transportation temperature. Transportation personnel must undergo professional training and be familiar with the characteristics of the compound and emergency treatment methods. In the event of an unexpected situation such as leakage, they can respond quickly and properly to reduce the harm.
In addition, whether it is storage or transportation, clear labels should be set up, indicating the name, nature, hazard and emergency treatment information of the compound, so that relevant personnel can identify and respond. In this way, the safety and stability of 7-methoxy-2,2,4-trimethyl-1,2-dihydroquinoline during storage and transportation must be ensured.