1e 1 3 3 3 Tetrafluoroprop 1 Ene
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
(1E)-1,3,3,3-tetrafluoroprop-1-ene
Chemical Formula C3H2F4
Molecular Weight 114.04
Boiling Point -19.9 °C
Melting Point -143.8 °C
Critical Temperature 109.4 °C
Critical Pressure 3.38 MPa
Flammability non - flammable
Odp Ozone Depletion Potential 0
Gwp Global Warming Potential 4
Vapor Density 3.94 kg/m³ (at 21.1 °C, 101.3 kPa)
Liquid Density 1206 kg/m³ (at -20 °C)
Chemical Formula C3H2F4
Molecular Weight 114.04
Boiling Point -28.4 °C
Melting Point -139 °C
Density 1.213 g/cm³ at 25 °C
Vapor Pressure 1283 kPa at 21.1 °C
Flammability non - flammable
Odp Ozone Depletion Potential 0
Gwp Global Warming Potential 4
Refrigerant Number R1234ze(E)
Chemical Formula C3H2F4
Molar Mass 114.04 g/mol
Boiling Point -19.5 °C
Melting Point -136 °C
Density 1.263 g/cm³ (at 25 °C)
Vapor Pressure 1240 kPa (at 21.1 °C)
Flammability non - flammable
Odp Ozone Depletion Potential 0
Gwp Global Warming Potential 4
Solubility In Water 0.026 g/L (at 25 °C)
Chemical Formula C3H2F4
Molecular Weight 114.04
Boiling Point -19.9 °C
Melting Point -139 °C
Vapor Pressure 1439 kPa at 21.1 °C
Density 1.213 g/cm³ at 20 °C
Flammability flammable
Odp Ozone Depletion Potential 0
Gwp Global Warming Potential 4
Solubility In Water low solubility
FAQ

What are the chemical properties of (1E) -1,3,3,3-tetrafluoropropene?

(1E) -1,3,3,3-tetrahydronaphthol, this physical property is also particularly well-researched. Its mild nature, solid at room temperature, nearly white and slightly transparent, like powder or crystal, dense texture.

Its melting degree is about a specific range, this value is the key to define its physical state change. When heated to a certain temperature, it converts into a liquid, and this transition is smooth and orderly. Its boiling degree is also characteristic. Under a specific pressure environment, it reaches a certain high temperature before boiling and vaporizing, both of which are related to its intermolecular force and structural density.

When it comes to solubility, (1E) -1,3,3,3-tetrahydronaphthol is mostly soluble in organic solvents. Alcohols and ethers, for example, can dissolve with them to form a uniform system. This is because its molecular structure contains specific groups, which can form interactions with organic solvent molecules such as hydrogen bonds, van der Waals forces, etc., and therefore blend.

And it has a certain chemical activity. Some bonds in the molecule are active and can participate in a variety of chemical reactions. In case of strong oxidizing agents, or oxidation changes, their structure or changes, and new products are produced. Under suitable catalytic conditions, it can involve reactions such as addition and substitution, and with its unique structure, it provides a variety of possibilities for reactions. It has great application potential in the field of organic synthesis and can be used as a key intermediate to produce many organic compounds with special properties.

What are the application fields of (1E) -1,3,3,3-tetrafluoropropylene?

(1E) -1,3,3,3-tetrahydronaphthol, also known as 1-ethyl-1,3,3,3-tetrahydronaphthol, has a wide range of application fields.

In the field of pharmaceutical synthesis, it can act as a key intermediate. With its unique chemical structure, compounds with specific pharmacological activities can be constructed through a series of chemical reactions. For example, in the synthesis of some antihistamine drugs, 1-ethyl-1,3,3,3-tetrahydronaphthol plays an important role in the construction of key parts of drug molecules, which in turn affects the interaction between drugs and receptors, which is related to drug efficacy and specificity. < Br >
In the field of materials science, it can be used to synthesize polymer materials with special properties. Its molecular structure imparts certain unique properties to the material, such as improving the thermal stability and mechanical properties of the material. For example, when preparing specific engineering plastics, the introduction of structural units derived from 1-ethyl-1,3,3-tetrahydronaphthol can enhance the heat resistance of plastics, so that they can still maintain good physical properties in high temperature environments, and broaden the application scenarios of engineering plastics, such as in automotive parts, electronic equipment shell manufacturing and other fields that require strict material properties.

In the fragrance industry, 1-ethyl-1,3,3-tetrahydronaphthol is also useful. Its unique odor characteristics can be used as a fragrance ingredient to prepare a unique flavor. In some high-end perfumes or air fresheners, trace amounts of this compound will be added to the formula to give the product a unique and attractive aroma, enhancing product quality and market competitiveness.

In addition, in the field of organic synthetic chemistry, 1-ethyl-1,3,3-tetrahydronaphthol, as a representative organic compound, is often used to explore new reaction pathways and catalytic systems. Chemists have developed more efficient and green organic synthesis methods through the study of its reaction properties, which has promoted the continuous development of organic synthetic chemistry.

What are the environmental effects of (1E) -1,3,3,3-tetrafluoropropylene?

(1E) -1,3,3,3-tetrafluoropropylene is a chemical substance. Its impact on the environment is related to many aspects.

This substance has a lower greenhouse effect potential in the atmosphere. Compared with the fluorine-containing compounds commonly used in the past, its impact on global warming is smaller. Due to its unique molecular structure and the characteristics of carbon-fluorine bonds, it is difficult to retain in the atmosphere for a long time, and there are few substances that can exacerbate the greenhouse effect after decomposition.

In terms of ozone layer effects, (1E) -1,3,3,3-tetrafluoropropylene has little damage to the ozone layer. In the past, chlorofluorocarbons would decompose chlorine atoms in the stratosphere under ultraviolet irradiation, and chlorine atoms would catalyze ozone decomposition, causing ozone layer depletion. However, this substance does not contain chlorine, so there is no such danger, which is of great benefit to the protection of the ozone layer.

And its chemical stability is still good. Under normal use conditions, it is not easy to react violently with other substances, will not cause complex chemical reaction chains in the environment, and has little disturbance to the balance of the ecosystem.

In terms of volatility, its volatility is moderate, neither too fast to evaporate and cause a large amount of short-term diffusion, nor too stable and long-term accumulation in the local environment. This characteristic allows it to better control its concentration and distribution in the environment during application.

Although (1E) -1,3,3,3-tetrafluoropropylene has many positive effects on the environment, it still needs to be carefully considered when it is used on a large scale. When the whole life cycle of its production, use and disposal is comprehensively evaluated to ensure that its long-term impact on the environment is within an acceptable range and achieve the goal of environmental friendliness and sustainable development.

What are the production methods for (1E) -1,3,3,3-tetrafluoropropylene?

The production methods of (1E) -1,3,3,3-tetrahydronaphthol are as follows:
One is the chemical synthesis method. First take a suitable aromatic compound, such as a derivative of naphthalene, and make it react with a specific reagent under suitable reaction conditions. If at a specific temperature and pressure, a metal catalyst is used to catalyze the hydrogenation reaction with hydrogen gas. This process requires precise control of the reaction temperature, pressure and catalyst dosage. If the temperature is too high or too low, the reaction rate may be abnormal or the product selectivity may be poor; improper pressure will also affect the reaction process. The type and dosage of catalyst have a great impact on the reaction activity and product purity. After this hydrogenation reaction, (1E) -1,3,3,3-tetrahydronaphthol can be gradually generated.
The second is biosynthesis. Find microorganisms with specific enzyme systems, such as certain bacteria or fungi. After screening and culturing, add suitable precursor substances to the microbial culture system. The enzymes in the microorganisms will play a catalytic role to promote the transformation of precursor substances. This process requires regulation of the culture environment, such as the composition of the medium, pH, temperature, dissolved oxygen, etc. If the medium composition is not suitable, the microorganisms will not grow well and the enzyme activity will be inhibited; pH, temperature, and dissolved oxygen deviate from the optimal range, which will affect the efficiency and direction of the enzymatic reaction, and ultimately affect the synthesis of (1E) -1,3,3,3-tetrahydronaphthol.
Third, it can be extracted from natural products. Some plants or organisms in nature contain such ingredients. First, the raw materials containing the target ingredients are collected, pulverized, extracted and other preliminary treatments, and suitable organic solvents, such as ethanol, ethyl acetate, etc., are used to dissolve (1E) -1,3,3,3-tetrahydronaphthol from the raw materials according to the principle of similar phase dissolution. After that, the extract is separated and purified by distillation, column chromatography and other separation methods to remove impurities and obtain high-purity (1E) -1,3,3,3-tetrahydronaphthol.

What are the advantages of (1E) -1,3,3,3-tetrafluoropropylene over other similar compounds?

Compared with other similar compounds, (1E) -1,3,3,3-tetrahydronaphthol has the advantage of its unique structure, which endows it with a series of excellent characteristics. The unique bridge-ring structure of this compound makes the molecule have high rigidity and stability. In chemical reactions, this structural feature makes it exhibit unique reactivity and selectivity.

Taking many organic synthesis reactions as an example, (1E) -1,3,3,3-tetrahydronaphthol can precisely guide the reaction direction during the reaction process, increase the proportion of target products, reduce the occurrence of side reactions, and effectively improve the yield and purity of the reaction. This efficient and accurate reaction performance is of great significance in the field of medicinal chemistry. The drug development process requires strict requirements for the purity and activity of compounds. The above advantages of (1E) -1,3,3,3-tetrahydronaphthol make it an ideal intermediate for the synthesis of specific drug molecules, which helps to simplify the synthesis steps, reduce production costs, and accelerate the process of new drug development.

From the perspective of physical properties, the rigid structure of the compound affects its intermolecular forces, resulting in a suitable melting point and solubility. This physical property has potential application value in the field of materials science. For example, it can be used as a key raw material for the preparation of specific functional materials, and its unique physical properties endow materials with special properties.

In addition, the unique structure of (1E) -1,3,3-tetrahydronaphthol also has outstanding performance in biological activity. Studies have shown that it can interact specifically with specific biological targets, exhibiting potential biological activities such as anti-inflammatory, antioxidant, etc., which lays a solid foundation for its further development and application in the field of medicine.