Chemical Formula | C14H14F3O2S |
Molecular Weight | 304.32 |
Appearance | Solid (predicted) |
Boiling Point | Estimated around 350 - 400 °C under normal pressure |
Solubility In Water | Low solubility, as it is an organic compound with non - polar groups |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, chloroform, etc. |
Density | Estimated based on similar structures, around 1.3 - 1.5 g/cm³ |
Vapor Pressure | Low vapor pressure at room temperature |
Chemical Formula | C13H12F3O2S |
Molecular Weight | 304.3 |
Appearance | Solid (likely) |
Physical State At Room Temp | Solid |
Solubility In Water | Low (due to non - polar groups) |
Solubility In Organic Solvents | Good in non - polar and some polar organic solvents |
Melting Point | Specific value would require literature search |
Boiling Point | Specific value would require literature search |
Stability | Stable under normal conditions, may react with strong oxidants/reductants |
Chemical Formula | C14H14F3O2S |
Molecular Weight | 304.32 |
Appearance | Solid (Typical) |
Melting Point | Data may vary, check specific sources |
Boiling Point | Data may vary, check specific sources |
Solubility In Water | Low solubility |
Solubility In Organic Solvents | Soluble in some organic solvents like dichloromethane |
Pka | Data may vary, check specific sources |
Logp | Data may vary, check specific sources |
Vapor Pressure | Low vapor pressure |
Chemical Formula | C13H13F3O2S |
Molecular Weight | 306.30 |
Appearance | Solid (usually) |
Melting Point | Specific value would need experimental determination |
Boiling Point | Specific value would need experimental determination |
Solubility In Water | Low (organic compound with non - polar groups) |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, chloroform |
Density | Specific value would need experimental determination |
Flash Point | Specific value would need experimental determination |
Stability | Stable under normal conditions, but may react with strong oxidizing agents |
What is the main use of 1-cyclopropyl-3- (2-methylthio-4-trifluoromethylphenyl) -1,3-propanedione?
The main use of 1-cyclopropyl-3- (2-methyl-4-trifluoromethylphenoxy) -1,3-propanediol is particularly important. This substance is very useful in the field of pharmaceutical synthesis.
covers its unique structure and can be used as a key intermediate when creating new drugs. For example, when developing targeted drugs for specific diseases, it can be integrated into the molecular structure of the drug through precise chemical reactions, enabling the drug to precisely act on the target of diseased cells. This property allows researchers to optimize the efficacy of the drug and reduce the adverse effects on normal cells.
In the field of pesticide development, 1-cyclopropyl-3- (2-methyl-4-trifluoromethylphenoxy) -1,3-propylene glycol also has important functions. It can be used as a raw material for the synthesis of high-efficiency and low-toxicity pesticides, because it imparts special physical and chemical properties to pesticide molecules, making pesticides more effective in killing and inhibiting pests and bacteria, and at the same time reducing the harm to the environment, in line with the current green agricultural development concept.
Furthermore, in the field of materials science, it also has potential uses. It may be able to integrate into polymer materials through appropriate chemical modification and polymerization reactions to improve the properties of materials, such as enhancing the stability and corrosion resistance of materials, providing new paths for the development of new materials. In short, 1-cyclopropyl-3- (2-methyl-4-trifluoromethylphenoxy) -1,3-propanediol has important value and wide application prospects in many fields.
What are the synthesis methods of 1-cyclopropyl-3- (2-methylthio-4-trifluoromethylphenyl) -1,3-propanedione?
To prepare 1-cyclopropyl-3- (2-methyl-4-trifluoromethylbenzyl) -1,3-propanediol, the following methods can be used.
First, the compound containing cyclopropyl is used as the starting material. First, the cyclopropane derivative undergoes a substitution reaction with a suitable reagent, and a suitable functional group is introduced to facilitate subsequent connection with the structural fragment containing (2-methyl-4-trifluoromethylbenzyl). In this process, attention should be paid to the mildness of the reaction conditions to avoid damage to the cyclopropyl structure. For example, when selecting a nucleophilic substitution reaction, carefully select the nucleophilic reagent, reaction solvent, temperature, etc., so that the substitution check point is accurate and controllable.
Second, for the (2-methyl-4-trifluoromethyl benzyl) part of the construction. It can start from methyl benzene derivatives, introduce halogen atoms at specific positions in the benzene ring through halogenation reaction, and then introduce trifluoromethyl by interacting with trifluoromethylation reagents. Then react with compounds containing active groups to construct benzyl structures. During this period, pay attention to the reaction selectivity to ensure the correct introduction of trifluoromethyl and other functional groups.
Third, connect the cyclopropyl-containing fragment with the (2-methyl-4-trifluoromethylbenzyl) fragment. Condensation reactions can be used, such as in the presence of appropriate catalysts, to react the active functional groups of the two to form carbon-carbon bonds or other connection bonds. At the same time, control the reaction conditions to prevent side reactions from occurring, such as excessive condensation or other unnecessary substitution reactions.
Fourth, for the introduction of 1,3-propylene glycol structure. On the basis of the above-mentioned connection products, the diol structure can be introduced through reduction, hydroxylation and other reactions. If a suitable reducing agent is used, some functional groups are reduced to hydroxyl groups, or hydroxyl groups are introduced through nucleophilic substitution reactions, and the hydroxyl groups are guaranteed to be in the same position as the target molecule.
In summary, the synthesis of 1-cyclopropyl-3- (2-methyl-4-trifluoromethylbenzyl) -1,3-propylene glycol requires multiple steps. The reaction conditions, reagent selection and reaction sequence of each step are all critical, and fine regulation is required to obtain the target product.
What are the physicochemical properties of 1-cyclopropyl-3- (2-methylthio-4-trifluoromethylphenyl) -1,3-propanedione
1-Cyclopropyl-3- (2-methyl-4-trifluoromethylbenzyl) -1,3-propanediol, this compound has unique physical and chemical properties. Its properties are usually white to off-white crystalline powder, which is relatively stable at room temperature and pressure.
When it comes to the melting point, it is usually in a specific temperature range, which is helpful for the identification and purification of the substance. The determination of the melting point can provide an important reference for its purity. If the purity is high, the melting point range is relatively narrow and close to the theoretical value.
In terms of solubility, it shows a certain solubility in organic solvents such as ethanol and acetone, but the solubility in water is relatively low. This difference in solubility is of great significance in the separation, extraction and preparation of compounds. With the help of its solubility characteristics in different solvents, it can effectively achieve separation from impurities, and can also design suitable dosage forms according to needs.
From the perspective of chemical stability, it is not easy to chemically react with common components in the air such as oxygen and carbon dioxide under conventional conditions. However, in extreme chemical environments such as strong acids and bases, the structure may change, triggering chemical reactions and generating new products. This requires that during storage and use, it is necessary to properly avoid contact with such substances.
The cyclopropyl, methyl, and trifluoromethyl groups in its molecular structure endow the compound with unique electronic effects and steric barriers. These structural characteristics not only affect their physical and chemical properties, but also have profound effects on their biological activities and pharmacological effects. For example, the strong electron-absorbing properties of trifluoromethyl may change the electron cloud distribution of molecules, which in turn affects their interaction with biological targets.
What is the price range of 1-cyclopropyl-3- (2-methylthio-4-trifluoromethylphenyl) -1,3-propanedione in the market?
The price of 1-cyclopropyl-3- (2-methyl-4-trifluoromethylphenoxy) -1,3-propanediol is actually related to various factors, and it is difficult to determine its exact number.
The price of this compound depends first on the difficulty of its preparation. If the preparation method is complicated, it requires all kinds of rare raw materials and harsh conditions, and the price will be high. If the exquisite organic synthesis technique is adopted, after multiple steps of reaction, each step needs to be precisely regulated. If there is a slight mistake, all previous efforts will be wasted, and its cost will be high, and it will be expensive in the market.
Furthermore, the state of market supply and demand also affects its price. If the demand for this product in the fields of medicine and chemical industry is strong, but the supply is limited, the price will increase. Just as the army needs this as a raw material for medicine, the dosage increases greatly, and it is difficult for producers to supply it in sufficient quantities in time, so the price rises. On the contrary, if the supply exceeds the demand, the price will decline.
The situation of origin and transportation also has an impact. If it is produced here and needs to be shipped to a distant place, it will cost freight, insurance, etc., and the price will increase when it arrives there. And if the taxes and labor costs of the place of origin are different, the initial price will also be different.
Overall, the price of 1-cyclopropyl-3- (2-methyl-4-trifluoromethylphenoxy) -1,3-propylene glycol often fluctuates between tens of yuan and hundreds of yuan per gram. However, this is only a rough figure. Market conditions change rapidly. The actual price should be subject to real-time consultation with suppliers or market transactions.
What are the manufacturers of 1-cyclopropyl-3- (2-methylthio-4-trifluoromethylphenyl) -1,3-propanedione?
There is no shortage of manufacturers of 1-cyclopropyl-3- (2-methylphenyl-4-trifluoromethylbenzoyl) -1,3-malondione in this world. These manufacturers, each with their own ability, use exquisite methods to make this stunner.
There is a factory in Shanghai, which has been studying the chemical synthesis for many years and has profound background. The craftsmen in the factory are all skilled and familiar with all kinds of reactions. When preparing this compound, the pure raw materials are carefully selected, and the reaction system is introduced according to the precise ratio. Under suitable temperature and pressure, it reacts ingeniously with related reagents, just like a microscopic dance, and the molecules fit in sequence. The follow-up steps are also seamless, and each step of transformation is treated like a beautiful jade, carefully and attentively. Finally, this 1-cyclopropyl-3- (2-methylphenyl-4-trifluoromethylbenzoyl) -1,3-malonate is of high quality and praised by the industry.
Furthermore, in Guangdong, there is also a factory that uses innovative ideas to prepare things. The factory is not limited by traditional methods and has the courage to try novel processes. Its scientific research team works day and night to optimize the reaction path from a unique perspective. When preparing, advanced equipment is used to precisely control the reaction process. From the screening of raw materials, to the transition of intermediate products, to the molding of the final product, it is all like flowing water in one go. The 1-cyclopropyl-3- (2-methylphenyl-4-trifluoromethylbenzoyl) -1,3-malondione produced is not only considerable in output, but also has a high purity. It is sold at home and abroad and has a great reputation.
There are also those who live in the land of Suzhou and Hangzhou, where the humanities are gathered and the chemical elite are also cultivated. Its factory prepares this product and pays attention to the way of green environmental protection. During the reaction process, we strive to reduce the generation of waste, make rational use of resources, and run through the concept of sustainability. Although the preparation road may be difficult, it adheres to its original intention and continuously improves the process. The 1-cyclopropyl-3- (2-methylphenyl-4-trifluoromethylbenzoyl) -1,3-malonate produced is not only in line with the current trend of environmental protection, but also of outstanding quality and is unique in the market.