3 4 Fluorophenyl Thio 2 Hydroxy 2 Methylpropanoic Acid
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
3-[(4-Fluorophenyl)thio]-2-hydroxy-2-methylpropanoic acid
Chemical Formula C10H11FO3S
Molecular Weight 230.26
Appearance Solid (Typical description, may vary)
Melting Point N/A (No data provided, actual value required for accurate info)
Boiling Point N/A (No data provided, actual value required for accurate info)
Solubility In Water N/A (No data provided, actual value required for accurate info)
Solubility In Organic Solvents N/A (No data provided, actual value required for accurate info)
Pka Value N/A (No data provided, actual value required for accurate info)
Flash Point N/A (No data provided, actual value required for accurate info)
Density N/A (No data provided, actual value required for accurate info)
Chemical Formula C10H11FO3S
Molar Mass 230.26 g/mol
Appearance Solid (presumably, based on similar compounds)
Solubility In Water Low (due to non - polar phenyl and thio groups)
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone
Acidity Pka Related to carboxylic acid group, around 4 - 5 (estimated for carboxylic acids)
Reactivity Reactive towards bases, nucleophiles at the carboxylic acid group and electrophiles at the thio - phenyl moiety
Chemical Formula C10H11FO3S
Molecular Weight 230.26
Appearance Solid (Typical)
Melting Point Data needed
Boiling Point Data needed
Solubility In Water Data needed
Solubility In Organic Solvents Data needed
Density Data needed
Pka Value Data needed
Flash Point Data needed
Chemical Formula C10H11FO3S
Molecular Weight 230.26
Appearance Solid (Typical)
FAQ

What are the chemical properties of 3- [ (4-fluorophenyl) thio] -2-hydroxy-2-methylpropionic acid?

3 - [ (4-hydroxybenzyl) benzyl] - 2-furyl-2-methylbutyric acid is an organic compound. It has specific chemical properties, let me tell you one by one.

This compound contains furan rings and specific substituents, which exhibit certain physical and chemical properties due to the connection of atoms in the structure and the distribution of electron clouds. From the perspective of chemical activity, the presence of furan rings makes it possible to participate in many reactions. Furan rings are electron-rich aromatic rings, which are nucleophilic and easily react with electrophilic reagents, such as electrophilic substitution reactions. Under suitable conditions, electrophilic reagents can attack the position with high electron cloud density on the furan ring, realize the introduction of substituents, and then derive a series of new compounds.

Furthermore, the methylbutyric acid part of the molecule contains carboxyl functional groups. The carboxyl group is acidic and can neutralize with the base to form the corresponding carboxylate and water. If this compound is placed in a basic environment, the carboxyl group will lose protons and form a carboxyl negative ion. This ion form is different from the neutral carboxyl group in stability and reactivity in some reactions or systems. At the same time, the carboxyl group can also participate in the esterification reaction, dehydration and condensation with alcohols under acid catalysis to form ester compounds.

And the complex benzyl substituent part in the compound, the benzyl ring in the benzyl group is connected to the methylene structure, which endows the molecule with a certain steric hindrance and electronic effect. The benzene ring can affect the electron cloud density of the surrounding groups through the conjugate system, changing the overall reactivity of the molecule. In addition, the hydrogen atom on the benzyl group can undergo reactions such as halogenation under appropriate conditions to realize the conversion and modification of functional groups, providing the possibility for the synthesis of more complex organic compounds.

In summary, 3- [ (4-hydroxybenzyl) benzyl] -2-furyl-2-methylbutyric acid has a variety of chemical properties due to its unique structure, and may have potential applications and research values in the fields of organic synthesis.

What are the main uses of 3- [ (4-fluorophenyl) thio] -2-hydroxy-2-methylpropionic acid?

3- [ (4-hydroxybenzyl) carbonyl] -2-furyl-2-methylbutyric acid, which is an important raw material in organic synthesis. In the field of organic synthesis, it plays multiple key roles.

One is often the starting material for the construction of complex organic molecules. With its special chemical structure, such as furan ring, methyl and carboxyl groups, chemists can modify and expand it through various chemical reactions to synthesize organic compounds with diverse structures and functions. For example, by esterification, its carboxyl group can be reacted with alcohols to generate ester compounds with specific properties, which are widely used in the fields of fragrances and drugs.

Second, it also plays an important role in the field of medicinal chemistry. Due to its structural characteristics, it may have certain biological activities. Researchers often use this as a basis to optimize and derive its structure to develop new drugs. For example, by changing the type and location of its substituents, the solubility, stability and affinity with biological targets of the drug can be adjusted, thereby improving the efficacy and safety of the drug.

Third, in the field of materials science, polymers or functional materials synthesized based on this compound may exhibit unique physical and chemical properties. If they have special optical, electrical or thermal properties, they can be applied to optoelectronic materials, polymer materials and other fields, providing new opportunities and directions for the development of materials science.

What is the synthesis method of 3- [ (4-fluorophenyl) thio] -2-hydroxy-2-methylpropionic acid?

To prepare 3- [ (4-cyanobenzyl) carboxyl] -2-furanyl-2-methylbutyric acid, the following method can be followed:

First, use suitable starting materials, such as furan derivatives with corresponding substituents, and react with reagents containing cyanobenzyl structures under suitable reaction conditions. This reaction may require nucleophilic substitution or condensation in organic solvents under the catalysis of bases, so that cyanobenzyl can be introduced into specific positions of the furan ring to form intermediates with (4-cyanobenzyl) structures attached to the furan ring. < Br >
Then, the cyanyl group in the intermediate is hydrolyzed. This hydrolysis can be carried out under the catalysis of an acid or a base to convert the cyanyl group into a carboxyl group, thereby obtaining a furan derivative intermediate containing the structure of [ (4-cyanobenzyl) carboxyl].

On the basis of this intermediate, methyl is introduced. Suitable methylation reagents, such as iodomethane, can be selected. Under the action of bases, methyl is introduced into a specific carbon site connected to the furan ring through nucleophilic substitution to form a 2-methyl structure.

Finally, the molecular structure is appropriately adjusted and modified to construct the backbone structure of butyric acid. Or through a series of carbon-carbon bond formation reactions, functional group conversion reactions, etc., the reaction conditions and reagents are carefully regulated, so that the structures of each part are precisely connected, and the final target product is 3 - [ (4-cyanobenzyl) carboxyl] - 2 -furyl-2 -methylbutyric acid. The entire synthesis process requires fine control of the reaction conditions at each step, including temperature, reaction time, reagent dosage, etc., and attention should be paid to the separation and purification of intermediates to ensure the efficient and smooth progress of the reaction and improve the yield and purity of the target product.

What are the precautions for storing 3- [ (4-fluorophenyl) thio] -2-hydroxy-2-methylpropionic acid?

3 - [ (4 -hydroxybenzyl) carboxyl] - 2 -furyl-2 -methylbutyric acid should pay attention to the following things when storing:

First, this compound has specific chemical activity and is quite sensitive to the storage environment. It should be placed in a low temperature, dry and well-ventilated place to avoid deterioration due to changes in temperature and humidity. High temperature or high humidity environment, or the compound undergoes hydrolysis, oxidation and other reactions, which damage its chemical structure and properties.

Second, because it contains a variety of functional groups, such as carboxyl, furan, etc., these groups may react chemically with other substances. Therefore, when storing, it is necessary to keep away from oxidizing agents, reducing agents, acids, alkalis and other chemically active substances to prevent unnecessary reactions. For example, carboxylic groups are prone to salt when exposed to alkali, or change their original properties.

Third, the compound may have certain volatility and hygroscopicity. It should be stored in a sealed container. Commonly used glass bottles or plastic bottles can be used, but it must be sealed tightly to prevent volatilization and moisture absorption. If using glass bottles, attention should be paid to the material. Some glass components may react weakly with compounds, which affects their quality.

Fourth, the storage process must be well marked, and key information such as the compound name, structural formula, storage date, and valid period must be recorded in detail. Periodically check the storage situation to see if there are any appearance changes, such as color changes, precipitation, etc. If there is any abnormality, it should be analyzed and dealt with in time.

In short, proper storage of 3- [ (4-hydroxybenzyl) carboxyl] -2-furyl-2-methylbutyric acid is essential to maintain its chemical stability and quality. It is necessary to strictly follow the relevant storage specifications and precautions during operation.

What is the market price of 3- [ (4-fluorophenyl) thio] -2-hydroxy-2-methylpropionic acid?

I look at what you said about "3 - [ (4 - tritium benzyl) silyl] - 2 - naphthyl - 2 - methylbutyric acid", which is an organic compound. As for its market price, it is difficult to say exactly. Because the price of organic compounds is often affected by many factors.

First, the purity has a great impact. If the purity of this compound is very high, it can be used for precision experiments or special industrial applications, and its price is high. However, if the purity is slightly lower, the price of materials used for general research or preliminary experiments is slightly lower.

Second, the difficulty of preparation is also the key. If the preparation of this compound requires cumbersome steps, special raw materials and conditions, and requires a lot of manpower, material resources and time, the cost will be high, and the market price will also rise. On the contrary, if the preparation is relatively simple, the price may be close to the people.

Third, the market supply and demand relationship cannot be ignored. If the market demand for this compound is strong, but the supply is limited, the merchant may raise the price. If there is little demand and sufficient supply, the price may fall.

Fourth, the production scale is also related to the price. In large-scale production, due to the scale effect, the unit cost may be reduced and the price may be more competitive. Small-scale production, the cost is difficult to reduce, and the price is also difficult to lower.

In summary, in order to know the exact market price of "3- [ (4-tritium benzyl) silyl] -2-naphthyl-2-methylbutyric acid", it is necessary to carefully investigate its purity, preparation difficulty, market supply and demand, and production scale. It is recommended to consult professional chemical raw material suppliers, chemical product trading platforms, etc. to obtain more accurate price information.