What is the chemical structure of 4,4,4-trifluoro-3-methylamino-butyl-2-enoic acid ethyl ester, (2Z)?

The chemical structure of 4,4,4-trifluoro-3-methoxy-butyl-2-enoic acid ethyl ester (2Z) is that it contains an ethyl ester group (-COOCH < unk > CH < unk >) connected to a double-bonded carbon atom. The double bond is Z-shaped (that is, two larger groups on the same side of the double bond), and the other side of the double bond is connected to a trifluoromethyl (-CF < unk >) and a methoxy (-OCH < unk >) butenic acid ethyl ester structure. This compound uses ethyl butenate as the parent body, and introduces trifluoromethyl and methoxy groups at specific positions. Each atom is connected in an orderly manner through chemical bonds to form a unique spatial structure. The carbonyl group (C = O) in the ethyl ester group forms a conjugated system with the double bond, which affects the physical and chemical properties of the compound. Trifluoromethyl changes the electron cloud distribution of the molecule due to its strong electron absorption, which affects the reactivity. Methoxy groups also play a role in molecular properties through their electron-giving effects. The entire molecular structure determines the characteristics and reaction behavior of the compound, and may have unique uses in organic synthesis and other fields.

What are the physical properties of 4,4,4-trifluoro-3-methylamino-butyl-2-enoic acid ethyl ester, (2Z)?

4,4,4-trifluoro-3-methoxy-acetoacetate ethyl ester, (2Z) The physical properties of this substance are as follows:

It is an organic compound, and it usually appears as a colorless to light yellow transparent liquid at room temperature and pressure. It has a certain volatility and can evaporate slowly in air. The relative density is smaller than that of water. If mixed with water, it will float on the water surface.

This substance is soluble in common organic solvents such as ethanol, ether, acetone, etc. This is because the organic groups in its molecular structure have similar chemical properties to organic solvents and follow the principle of "similar miscibility". The boiling point of

is within a certain range, and the specific value will vary slightly due to experimental conditions and purity. Generally speaking, it will boil at a certain temperature range under a specific pressure. By controlling the pressure and temperature, it can be distilled and purified. The melting point of

also has a specific value. When the temperature drops below the melting point, the substance will change from a liquid state to a solid state.

The refractive index is a fixed value, which can be used to identify the purity of a substance and determine its molecular structure characteristics. By accurately measuring the refractive index, it can assist in judging whether the substance is pure and whether there is impurity interference.

These physical properties are of crucial significance for the separation, purification, identification, and participation in the control of chemical reaction conditions for 4,4,4-trifluoro-3-methoxy-acetoethyl acetate (2Z) in practical production and scientific research applications.

What are the synthesis methods of 4,4,4-trifluoro-3-methylamino-butyl-2-enoic acid ethyl ester, (2Z)?

To prepare 4% 2C4% 2C4-triene-3-methylhydroxy-hexyl-2-ethyl acetate, (2Z), the method is as follows:
The first is the choice of raw material. The corresponding carbon frame and functional group can be used as the starting material, such as compounds containing alkynyl groups, alkenyl groups and groups that can be converted into carboxyl ethyl esters. Or those with similar structures in natural products are obtained by modification and modification.
The second is the change of functional group. If the raw material contains suitable alkynyl groups, alkenyl groups and hydroxyl groups can be introduced by means of nucleophilic addition and oxidation. If a metal alkynide is reacted with an alkenyl-containing halogen to form an alkenyl structure; after oxidation, the alkenyl group is formed into a hydroxyl group.
can also be reacted to ethyl by esterification. If you have obtained 4% 2C4% 2C4-triene-3-methylhydroxyl-hexyl-2-alkynic acid containing carboxyl groups, you can form the corresponding ethyl ester with ethanol under the action of acid catalysis or condensation agent. If catalyzed by concentrated sulfuric acid, or assisted by condensation agents such as dicyclohexyl carbodiimide (DCC).
The control of stereochemistry is also heavy. To obtain the (2Z) configuration, suitable reagents and conditions need to be selected in the reaction. For example, some metal-catalyzed reactions can be regulated by ligands to make the alkenyl group have a (Z) configuration. During the alkenylation reaction, the reagent with stereoselectivity is selected, such as in the Weitixi reaction, the appropriate Ylide is selected to obtain the desired configuration.
In addition, the reaction sequence also affects the success or failure. The carbon frame is constructed first, and then the functional groups are modified one by one to avoid side reactions. For example, the alkenyl structure is formed first, followed by the introduction of hydroxyl and carboxyl groups, and finally esterification.
After each step of the reaction, the product needs to be purified by chromatography, recrystallization, etc. to achieve high purity and meet subsequent needs. Thus, through multi-step design and operation, 4% 2C4% 2C4-triene-3-methylhydroxy-hexyl-2-ethyl acetate, (2Z) can be obtained.

What are the application fields of 4,4,4-trifluoro-3-methylamino-butyl-2-enoic acid ethyl ester, (2Z)?

4,4,4-trifluoro-3-methoxy-butyl-2-enoic acid ethyl ester, (2Z), is useful in various fields such as medicine, pesticides and materials science.

In the field of medicine, this compound may be involved in drug synthesis. Due to its unique structure, fluorine-containing atoms can increase the lipophilicity of molecules, affecting the ability of drugs to bind to targets and metabolic processes in vivo. Its enoic acid ethyl ester structure may be a key fragment for the construction of active molecules, helping to develop new therapeutic drugs, such as anti-cancer and anti-viral drugs. With its special structure and biological activity, it acts on specific biological targets and achieves the purpose of treating diseases.

In the field of pesticides, this compound may be used as an important intermediate for the creation of new pesticides. The fluorine-containing structure gives it good biological activity and stability, or it can develop high-efficiency, low-toxicity, and environmentally friendly insecticides, fungicides or herbicides. With its special chemical structure, it precisely acts on the specific physiological processes of pests, achieving the effect of preventing and controlling pests and safeguarding crop growth.

In the field of materials science, 4,4,4-trifluoro-3-methoxy-butyl-2-enoic acid ethyl ester, (2Z) or can participate in the preparation of functional materials. For example, in the synthesis of polymer materials, special functional groups are introduced as comonomers to change the physical and chemical properties of the material, such as improving the thermal stability, chemical resistance or optical properties of the material, in order to meet the needs of different fields such as electronics and optics for special materials.

How safe is 4,4,4-trifluoro-3-methylamino-butyl-2-enoic acid ethyl ester, (2Z)?

The safety of this "4,4,4-trifluoro-3-methoxy-butyl-2-enoic acid ethyl ester, (2Z) " needs to be reviewed in detail.

First of all, in terms of its chemical properties, fluorine-containing groups often have unique properties. Fluorine atoms are highly electronegative, which will cause molecules to exhibit special reactivity and stability. The trifluoride structure in this substance may affect its chemical stability and reactivity with other substances. When storing, it is necessary to consider whether it will decompose or undergo other chemical reactions due to environmental factors, such as changes in temperature and humidity, which will affect safety.

Furthermore, the presence of methoxy groups also has an impact. The methoxy group acts as the power supply group, or has an effect on the overall electron cloud distribution of the molecule, affecting its chemical activity. From the perspective of toxicity, although there is no conclusive information that the methoxy group alone will cause high toxicity, it cooperates with other groups or produces different effects.

The ethyl alkenate structure contains carbon-carbon double bonds and ester groups. Carbon-carbon double bonds have high reactivity and are prone to reactions such as addition and oxidation. Under certain conditions, in case of strong oxidants, high temperatures, etc., or cause violent reactions. Ester groups are relatively stable, but in acid-base environments, hydrolysis reactions may occur.

From the perspective of industrial application scenarios, if used in production, its safety in the reaction process is crucial. It is necessary to strictly control the reaction conditions, such as temperature, pressure, proportion of reactants, etc., to prevent uncontrolled reactions. During transportation and storage, choose the appropriate packaging materials and storage environment according to their chemical characteristics to avoid leakage and deterioration.

In laboratory research scenarios, operators need to take protective measures. Due to the complexity of the chemical structure, there may be unknown latent risks. Appropriate protective equipment should be worn, such as gloves, goggles, protective clothing, etc., and the operation should be carried out in a well-ventilated environment to prevent inhalation or contact from causing harm.

In summary, although the safety of "4,4,4-trifluoro-3-methoxy-butyl-2-enoic acid ethyl ester, (2Z) " cannot be determined drastically, it needs to be carefully considered from various aspects to ensure safe use in all aspects.