2r 3r 2 2 4 Difluorophenyl 1 1h 1 2 4 Triazol 1 Yl Butane 2 3 Diol Methanesulfonate
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
(2R,3R)-2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)butane-2,3-diol methanesulfonate
Chemical Name (2R,3R)-2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)butane-2,3-diol methanesulfonate
Molecular Formula C14H18F2N4O5S
Molecular Weight 392.38 g/mol
Appearance Typically a solid (but may vary depending on purity and preparation)
Solubility Solubility characteristics can vary; may have some solubility in polar organic solvents
Melting Point Data specific to this compound's melting point would need to be experimentally determined
Pka pKa values would depend on the acidic/basic functional groups present and require experimental determination
Stability Stability can be affected by factors like temperature, humidity, and light
Crystal Structure Crystal structure details would require X - ray crystallography studies
Optical Rotation As it has chiral centers, it will exhibit optical rotation; specific value needs experimental measurement
Chemical Name (2R,3R)-2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)butane-2,3-diol methanesulfonate
Molecular Formula C15H19F2N3O5S
Molecular Weight 391.39
Appearance Typically a solid
Physical State Solid at room temperature
Solubility Solubility characteristics would depend on the solvent; may have limited solubility in water
Melting Point Specific melting point data would require experimental determination
Boiling Point Boiling point would also need experimental determination
Pka Acid - base properties (pKa) would need to be determined through analysis
Logp Lipophilicity (logP) would require experimental or computational assessment
Crystal Structure Crystal structure details would be obtained from X - ray crystallography studies
Chemical Name (2R,3R)-2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)butane-2,3-diol methanesulfonate
Chemical Name (2R,3R)-2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)butane-2,3-diol methanesulfonate
FAQ

What is the chemical structure of (2R, 3R) 2- (2,4-difluorophenyl) -1- (1H-1,2,4-triazole-1-yl) butane-2,3-diol methanesulfonate?

This is the structural description of the organic compound, and I want to know the details.

" (2R, 3R) -2- (2,4-difluorophenyl) -1- (1H-1,2,4-triazole-1-yl) butyl-2,3-diol anhydride", where " (2R, 3R) " characterizes the configuration of carbon atoms 2 and 3 in the molecule as R type, which is determined according to the Cahn-Ingold-Prelog rule, which is related to the spatial arrangement of atoms or groups.

"2- (2,4 -difluorophenyl) " indicates that a phenyl group is connected at the second position of the main chain, and the 2,4 positions of the phenyl group are replaced by fluorine atoms. Phenyl is a cyclic structure composed of six carbon atoms, which is aromatic; fluorine atoms are extremely electronegative elements, and their substitution has a great influence on the properties of compounds.

"1- (1H-1,2,4-triazole-1-group) " means that the first position of the main chain is connected to 1H-1,2,4-triazole-1-group. 1,2,4-triazole is a five-membered heterocycle containing three nitrogen atoms, which is common in many organic reactions and bioactive substances.

"Butane-2,3-diol anhydride" indicates that the main chain is a butane structure of four carbon atoms, and it is originally a diol structure at the 2nd and 3rd carbon atoms, and then forms an acid anhydride. Acid anhydride is formed by dehydration of two-molecule carboxylic acid and has unique chemical activity.

Overall, the structure of this compound fuses a variety of functional groups, and each part interacts, giving it specific physical and chemical properties, which may be of great significance in the fields of organic synthesis, medicinal chemistry, etc.

What are the main uses of (2R, 3R) 2- (2,4-difluorophenyl) -1- (1H-1,2,4-triazole-1-yl) butane-2,3-diol methanesulfonate?

(2R, 3R) 2- (2,4-dichlorophenyl) -1- (1H-1,2,4-triazole-1-yl) -1-butanone-2,3-dimethylsuccinate is an organic compound that has important uses in many fields.

In the field of medicine, it is often used as a key intermediate in the synthesis of antifungal drugs. The 1,2,4-triazole group in the structure of this compound contributes a lot to the antifungal activity. Through specific chemical reactions, it can be converted into antifungal agents with good efficacy, such as itraconazole. These drugs have significant efficacy in the treatment of a variety of fungal infections, such as dermatophytosis, deep fungal infections, etc., and bring good news to patients' health.

In the field of agriculture, the compound or its derivatives can be used as a fungicide. Because of its inhibitory activity against certain plant pathogens, when applied to crops, it can effectively prevent pathogenic bacteria from invading, reduce the incidence of crops, improve crop yield and quality, and help agricultural harvest.

In the field of organic synthetic chemistry, it is an extremely important synthetic building block. Because of its unique structure and multiple reactive check points, chemists can use various organic reactions to modify and derive. By introducing different substituents, new organic compounds with diverse structures can be synthesized, providing rich materials and new directions for the development of organic synthetic chemistry, and promoting the continuous progress of this field.

What are the physical properties of (2R, 3R) 2- (2,4-difluorophenyl) -1- (1H-1,2,4-triazole-1-yl) butane-2,3-diol methanesulfonate?

(2R, 3R) - 2 - (2,4 - dichlorophenyl) - 1 - (1H - 1,2,4 - triazole - 1 - yl) butyl - 2,3 - glycol acetate is an organic compound. Its physical properties are critical and have far-reaching implications for its applications in various fields.

The appearance of this compound is often white to off-white crystalline powder with fine texture. This form is easy to store and transport, and it is easy to handle in subsequent processing applications.

Melting point is one of its important physical properties. Generally speaking, the melting point of this compound is within a specific range, and this characteristic can be used to determine purity. If the melting point is accurate and the melting range is narrow, it often means higher purity. This is crucial in the quality control process to ensure that the product meets the established standards.

In terms of solubility, (2R, 3R) -2- (2,4-dichlorophenyl) -1- (1H-1,2,4-triazole-1-yl) butyl-2,3-diol acetate exhibits some solubility in some organic solvents, such as methanol and ethanol. However, the solubility in water is relatively poor. This solubility characteristic makes it play different roles in different chemical reactions and preparation of preparations. For example, in organic synthesis reactions, the appropriate reaction solvent can be selected according to its solubility to promote the smooth progress of the reaction; in the development of preparations, it is necessary to consider its solubility to design the dosage form to ensure that the active ingredients of the drug can be released properly.

In addition, the density of the compound is also a specific value. Although this value may not be as concerned as melting point and solubility in daily applications, it is also an indispensable consideration in some industrial production or scientific research scenarios with strict requirements for density, which affects its distribution and behavior in the system.

What is the synthesis method of (2R, 3R) 2- (2,4-difluorophenyl) -1- (1H-1,2,4-triazole-1-yl) butane-2,3-diol methanesulfonate?

What is the synthesis method of (2R, 3R) -2- (2,4-difluorophenyl) -1- (1H-1,2,4-triazole-1-yl) -butyl-2,3-diol benzoate? According to the classical Chinese format of "Tiangong Kaiwu", the answer is as follows:

To prepare (2R, 3R) -2- (2,4-difluorophenyl) -1- (1H-1,2,4-triazole-1-yl) -butyl-2,3-diol benzoate, it can be done by number method. First, the starting material can be reacted in a series to form the target product.

First take a suitable compound containing 2,4-difluorophenyl, and a reagent containing 1H-1,2,4-triazole-1-group, under appropriate reaction conditions, such as selecting a suitable solvent, controlling the appropriate temperature and pH, so that the two react to obtain an intermediate product. This process needs to pay attention to the precise control of the reaction conditions, otherwise it is prone to side reactions and impure products.

Then, the obtained intermediate product, and the substance containing the butyl-2,3-diol structure, and then through a specific reaction or condensation, so that the two are connected. This step also requires careful selection of reaction conditions and suitable catalysts to promote the efficient progress of the reaction.

Finally, the obtained product is reacted with benzoic acid or its active derivatives under suitable conditions to form an ester bond to obtain (2R, 3R) -2- (2,4-difluorophenyl) -1- (1H-1,2,4-triazole-1-yl) -butyl-2,3-diol benzoate. After each step of reaction, it needs to be separated and purified, such as extraction, distillation, recrystallization, etc., to improve the purity of the product. In this way, through a series of delicate reactions and treatments, the desired (2R, 3R) -2- (2,4-difluorophenyl) -1- (1H-1,2,4-triazole-1-yl) -butyl-2,3-diol benzoate can be obtained.

What is the market outlook for (2R, 3R) 2- (2,4-difluorophenyl) -1- (1H-1,2,4-triazole-1-yl) butane-2,3-diol methanesulfonate?

There is a product named (2R, 3R) -2- (2,4-difluorophenyl) -1- (1H-1,2,4-triazole-1-yl) -1-butene-2,3-dicarboxylic anhydride. To know the market prospect of this product, let me tell you.

This compound may have potential applications in the field of medicinal chemistry. Among them, the combination of 2,4-difluorophenyl and 1,2,4-triazolyl gives it unique chemical properties and biological activities. In pharmaceutical research and development, such structures are often a key part of the exploration of new antibacterial, antiviral and even anti-tumor drugs.

In the current pharmaceutical market, the demand for new specific drugs is increasing day by day. In terms of antibacterial drugs, the rampant spread of drug-resistant bacteria makes it urgent to develop new antibacterial agents. If this compound can show effective activity against drug-resistant bacteria, its market potential is immeasurable. The same is true in the field of antivirus. New viruses continue to emerge, and high-efficiency antiviral drugs are urgently needed. The market for anti-tumor drugs is broader, and many patients are eagerly looking forward to better therapeutic drugs.

Looking at the chemical industry, it may be used as an intermediate for the synthesis of other fine chemicals. With its unique structure and chemical modification, it can derive a variety of compounds with special properties, which can be used in coatings, plastic additives and other industries to broaden its market application range.

However, its market prospects are also facing challenges. The R & D process requires a lot of manpower, material resources and time to determine its safety and effectiveness. And the market competition is fierce, many pharmaceutical companies are exploring similar active compounds. Only by virtue of efficient R & D, excellent quality and reasonable marketing strategies can they win a place in the market.

In summary, (2R, 3R) 2- (2,4 -difluorophenyl) -1- (1H - 1,2,4 -triazole - 1 -yl) -1 -butene - 2,3 -dicarboxylic anhydride Although there are addressable market opportunities, it is also necessary to carefully deal with many challenges in order to shine in the market.