2s 2 2 Amino 5 Chlorophenyl 4 Cyclopropyl 1 1 1 Trifluorobut 3 Yn 2 Ol Methanesulfonate 1 1 5
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
(2S)-2-(2-AMINO-5-CHLOROPHENYL)-4-CYCLOPROPYL-1,1, 1-TRIFLUOROBUT-3-YN-2-OL METHANESULFONATE (1:1.5)
Chemical Name (2S)-2-(2 - AMINO - 5 - CHLOROPHENYL)-4 - CYCLOPROPYL - 1,1,1 - TRIFLUOROBUT - 3 - YN - 2 - OL METHANESULFONATE (1:1.5)
Chemical Name (2S)-2-(2-amino-5-chlorophenyl)-4-cyclopropyl-1,1,1-trifluorobut-3-yn-2-ol methanesulfonate (1:1.5)
Molecular Formula C14H15ClF3NO4S
Molecular Weight 385.8 g/mol
Appearance Solid (predicted)
Melting Point N/A (no data found)
Boiling Point N/A (no data found)
Pka N/A (no data found)
Logp N/A (no data found)
Stereochemistry S - configuration at chiral center
Chemical Name (2S)-2-(2 - AMINO - 5 - CHLOROPHENYL)-4 - CYCLOPROPYL - 1,1,1 - TRIFLUOROBUT - 3 - YN - 2 - OL METHANESULFONATE (1:1.5)
Chemical Name (2S)-2-(2 - AMINO - 5 - CHLOROPHENYL)-4 - CYCLOPROPYL - 1,1,1 - TRIFLUOROBUT - 3 - YN - 2 - OL METHANESULFONATE (1:1.5)
FAQ

What is the chemical structure of (2S) -2- (2-amino-5-chlorophenyl) -4-cyclopropyl-1,1,1-trifluorobutyl-3-alkyne-2-ol methanesulfonate (1:1.5)?

This is a question about the structure of organic compounds, but the name is slightly complicated and uncommon in the nomenclature of organic chemistry. In the style of "Tiangong Kaiwu", the answer is as follows:

Fu (2S) -2- (2-hydroxy-5-chlorophenyl) -4-cyclopropyl-1,1,1-trifluoro-3-butene-2-pentenoic anhydride (1:1.5), its structure is described as follows:

First, its main body is based on pentenoic anhydride, which is similar to the beam and column structure of a building. In the second position of pentenoic anhydride, according to the (2S) configuration, a substituent is attached. This substituent contains 2-hydroxy-5-chlorophenyl, which is like a delicate member suspended on a beam. Looking at it again, the 4 positions are connected with cyclopropyl, which seems to have a ring-like ornament, adding its unique structure. For the 1,1,1-trifluoride, if three pearls are placed on the side, their chemical properties are changed. The structure of 3-butene, and a flexible double bond is added to the main chain, making this compound more active.

In this way, the groups are connected in a specific order and configuration, forming the unique chemical structure of (2S) -2- (2-hydroxy-5-chlorophenyl) -4-cyclopropyl-1,1,1-trifluoro-3-butene-2-pentenoic anhydride (1:1.5), which may have different chemical and physical properties due to the interaction of each group, and may be useful in various fields such as organic synthesis and medicinal chemistry.

What are the main uses of (2S) -2- (2-amino-5-chlorophenyl) -4-cyclopropyl-1,1,1-trifluorobutyl-3-alkyne-2-ol methanesulfonate (1:1.5)?

(2S) 2- (2-hydroxy-5-bromophenyl) -4-cyclopropyl-1,1,1-trifluoro-3-butene-2-heptanoic anhydride (1:1.5) This substance is widely used. In the field of medicine, it is often used as a key intermediate to assist in the synthesis of drugs with specific biological activities. Due to its unique chemical structure, it can participate in a variety of chemical reactions, modify and transform to generate drug molecules that can act on specific targets, or have therapeutic effects on certain diseases.

In the field of materials science, it also has important applications. Because it contains special groups, or can impart specific properties to materials, such as improving the thermal stability and chemical stability of materials, or affecting the optical and electrical properties of materials, it plays an important role in the research and development of new functional materials.

In the field of organic synthetic chemistry, as an important reagent, it provides new strategies and methods for organic synthesis routes. With the help of its structural properties, the construction of special organic compounds is realized, and the development of organic synthetic chemistry is promoted, providing the possibility for the creation of organic molecules with novel structures and unique functions. In short, this compound has important uses in many scientific research and industrial fields, and is of great significance to the development of related fields.

What is the synthesis method of (2S) -2- (2-amino-5-chlorophenyl) -4-cyclopropyl-1,1,1-trifluorobutyl-3-alkyne-2-ol methanesulfonate (1:1.5)?

To prepare\ ((2S) -2- (2-hydroxy-5-bromophenyl) -4-cyclopropyl-1,1,1-trifluoro-3-butene-2-glutaric anhydride (1:1.5) \), the synthesis method is as follows:

First find a suitable starting material, using a compound containing cyclopropyl, bromophenyl and related alkenyl structures as the base, and select the appropriate reaction path according to the principle of organic synthesis.

First take an enol compound containing a specific structure and react with halogenated cyclopropane under the catalysis of a base. The alkali can be selected from potassium carbonate or the like, in an organic solvent such as\ (N, N-dimethylformamide (DMF) \), the temperature is moderately controlled, so that the reaction occurs smoothly, and the alkenyl intermediate containing cyclopropyl is obtained.

times, this intermediate is combined with bromophenol derivatives, catalyzed by metal catalysts such as palladium catalysts, and cross-coupling reactions are carried out under the synergistic action of ligands. The ligand can be selected from\ (2-dicyclohexylphosphine-2 ', 6' -dimethoxy biphenyl, under the protection of inert gas, and reacted in a suitable solvent such as toluene to obtain an enol intermediate containing bromophenyl and cyclopropyl.

Then, this intermediate is oxidized, such as hydrogen peroxide or m-chloroperoxybenzoic acid, and the oxidized enol structure is carbonyl, and then under acidic conditions, the carbonyl group and the ortho-carboxyl group undergo intramolecular condensation reaction to form an anhydride structure. Adjust the reaction conditions, such as temperature control, reaction time control and proportion of reactants, so that the product reaches the ratio requirement of\ ((2S) -2- (2-hydroxy-5-bromophenyl) -4-cyclopropyl-1,1,1-trifluoro-3-butene-2-glutaric anhydride (1:1.5) \). After separation and purification, such as column chromatography, the target product can be purified.

What are the physicochemical properties of (2S) -2- (2-amino-5-chlorophenyl) -4-cyclopropyl-1,1,1-trifluorobutyl-3-alkyne-2-ol methanesulfonate (1:1.5)?

(This is an extremely complex organic compound. According to your book, its name is (2S) -2- (2-hydroxy-5-bromophenyl) -4-cyclopropyl-1,1,1-trifluoro-3-oxo-2-pentenoate (1:1.5). This compound has unique physical and chemical properties, so let me tell you one by one.)

Its physical properties are usually solid or oily liquid, depending on the temperature and pressure of the surrounding environment. If the temperature is low, the molecular movement slows down, and the attractive force makes the substance tend to be solid, and the texture may be hard and have a certain crystalline form; if the temperature rises, the molecule is energized and the movement intensifies, it may be converted into an oily liquid, and the fluidity is enhanced.

Its melting point and boiling point are also key physical properties. The melting point is determined by the intermolecular force. There are hydrogen bonds, van der Waals forces, etc. between the molecules of the compound, resulting in its melting point or a specific range, which needs to be accurately determined by experiments. The same is true for the boiling point. The stronger the intermolecular force, the higher the energy required for gasification, and the higher the boiling point.

The solubility cannot be ignored, because it contains polar groups such as hydroxyl groups and ester groups, which may have certain solubility in polar solvents (such as water and ethanol), but also contains bromophenyl groups, cyclopropyl groups and other non-polar parts. It also has a certain solubility in non-polar solvents (such as benzene and carbon tetrachloride). The specific solubility varies depending on the type of solvent and the structural details of the compound.

In terms of its chemical properties, hydroxyl groups are active and easy to participate in substitution reactions. Ester groups can be hydrolyzed when exposed to acids or bases. Hydrolyzed into carboxylic acids and alcohols under acidic conditions, and carboxylic salts and alcohols under alkaline conditions.

Furthermore, the double bond is an active reaction check point, and an addition reaction can occur, which is added with hydrogen to form a saturated compound and with halogen to form a halogenated hydrocarbon. Although cyclopropyl is stable, it can also open the ring under specific conditions, showing unique chemical activities.

The physical and chemical properties of this compound are rich and diverse, and it may have important application value in organic synthesis, medicinal chemistry and other fields. However, in-depth experimental investigation is required to accurately grasp its characteristics.

What are the market prospects for (2S) 2- (2-amino-5-chlorophenyl) -4-cyclopropyl-1,1,1-trifluorobutyl-3-alkyne-2-ol methanesulfonate (1:1.5)?

What is the future of (2S) 2- (2-hydroxy-5-bromophenyl) -4-cyclopropyl-1,1,1-trifluorobutyl-3-ene-2-ylbenzoate (1:1.5) in the market? I will use the ancient classical saying of "Tiangong Kaiwu" to solve this doubt for you.

Today there is a thing called (2S) 2- (2-hydroxy-5-bromophenyl) -4-cyclopropyl-1,1,1-trifluorobutyl-3-ene-2-ylbenzoate in a ratio of 1:1.5. This substance combines all kinds of properties. The structure of its 2-hydroxy and 5-bromophenyl groups endows it with specific chemical activities; the unique configuration of 4-cyclopropyl to add its molecules; the part of 1,1,1-trifluorobutyl-3-ene-2-ylbenzoate makes it have different physical and chemical properties.

In the market, the prospect may be promising. Looking at today's world, chemical medicine, material research and development, many fields are booming. The unique structure of this substance, or in the way of pharmaceutical synthesis, is a key intermediate. Its fluoride-containing part can affect the lipophilicity and metabolic stability of the drug, making it easier for the drug to penetrate the biofilm and improve the curative effect. And the cyclopropyl structure can change the steric resistance and electronic effect of compounds, or help to develop new specific drugs, if used for antibacterial and anti-tumor drugs, or can make a contribution.

In the field of materials, because of its special structure, it may be able to prepare high-performance functional materials. If used in optical materials, the conjugate system and special substituents in its structure may endow the material with unique optical properties, such as fluorescence, photochromic, etc., which can be applied to display technology, anti-counterfeiting labels, etc. And because of its fluorine-containing groups, it may improve the weathering resistance and chemical corrosion resistance of materials, and may have a place to show its skills in construction, aviation and other fields that require strict material properties.

However, if you want to make it shine in the market, you also need to overcome various difficulties. The optimization of the synthesis process to reduce costs and improve purity is the top priority. In addition, marketing activities also need to focus on making various industries aware of their strengths in order to expand applications, open up sales, and achieve some prospects.