Linshang Chemical
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1,3-Dichloro-2-Fluoro-5-(Trifluoromethyl)Benzene
Linshang Chemical
|
HS Code |
405225 |
| Chemical Formula | C7H2Cl2F4 |
| Molecular Weight | 230.99 |
| Appearance | Colorless to light yellow liquid |
| Boiling Point | 158 - 160 °C |
| Melting Point | N/A |
| Density | 1.53 g/cm³ |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in common organic solvents |
| Vapor Pressure | N/A |
| Flash Point | 59 °C |
| Refractive Index | 1.438 |
As an accredited 1,3-Dichloro-2-Fluoro-5-(Trifluoromethyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500 - gram bottle packaging for 1,3 - dichloro - 2 - fluoro - 5 - (trifluoromethyl)benzene. |
| Storage | 1,3 - Dichloro - 2 - fluoro - 5 - (trifluoromethyl)benzene should be stored in a cool, well - ventilated area, away from heat, sparks, and open flames as it is likely flammable. Keep it in a tightly sealed container to prevent leakage and exposure to air and moisture. Store it separately from oxidizing agents and incompatible substances to avoid potential reactions. |
| Shipping | 1,3 - Dichloro - 2 - fluoro - 5 - (trifluoromethyl)benzene is a chemical. Shipping should comply with hazardous materials regulations. It may need proper packaging, labeling, and be transported by carriers licensed for such chemicals. |
Competitive 1,3-Dichloro-2-Fluoro-5-(Trifluoromethyl)Benzene prices that fit your budget—flexible terms and customized quotes for every order.
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Where to Buy 1,3-Dichloro-2-Fluoro-5-(Trifluoromethyl)Benzene in China?
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Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
As a leading 1,3-Dichloro-2-Fluoro-5-(Trifluoromethyl)Benzene supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
What are the main uses of 1,3-dichloro-2-fluoro-5- (trifluoromethyl) benzene?
1% 2C3 -dideuterium-2 -deuterium-5- (trideuterium methyl) benzene, although this substance is not detailed in Tiangong Kaiji, it is widely used based on current knowledge.
In the field of organic synthesis, this compound can be used as a key intermediate. Because it contains a specific deuterated group, it can be chemically converted and introduced into the target molecule. For example, in drug development, deuterated drugs are in the ascendant, and the introduction of deuterium atoms can change the metabolic pathway of the compound, increase its stability and half-life, and improve its efficacy. The deuterated structure of this compound may provide a cornerstone for the creation of new deuterated drugs. After delicate design reactions, it can be constructed into the molecular framework of drugs, opening up new paths for the development of new drugs.
In the field of materials science, it also has potential value. It can participate in the construction of polymer materials through specific reactions. Because of its deuterated properties, it may endow materials with unique physical and chemical properties, such as changing the thermal stability and optical properties of materials. In optical materials, the absorption and emission characteristics of materials at specific wavelengths can be adjusted to be suitable for optoelectronic devices, display materials and other fields.
In the level of scientific research, it can be used as a tracer. Due to the unique physical properties of deuterium and hydrogen, in chemical reactions or biological processes, deuterium atom traces can be detected to clarify the reaction mechanism, material transfer and metabolic pathways. For example, in the study of metabolism in organisms, specific biomolecules can be tagged with them, and tracked by precise analysis methods to gain insight into the mysteries of microscopic biochemical processes in organisms.
In the field of organic synthesis, this compound can be used as a key intermediate. Because it contains a specific deuterated group, it can be chemically converted and introduced into the target molecule. For example, in drug development, deuterated drugs are in the ascendant, and the introduction of deuterium atoms can change the metabolic pathway of the compound, increase its stability and half-life, and improve its efficacy. The deuterated structure of this compound may provide a cornerstone for the creation of new deuterated drugs. After delicate design reactions, it can be constructed into the molecular framework of drugs, opening up new paths for the development of new drugs.
In the field of materials science, it also has potential value. It can participate in the construction of polymer materials through specific reactions. Because of its deuterated properties, it may endow materials with unique physical and chemical properties, such as changing the thermal stability and optical properties of materials. In optical materials, the absorption and emission characteristics of materials at specific wavelengths can be adjusted to be suitable for optoelectronic devices, display materials and other fields.
In the level of scientific research, it can be used as a tracer. Due to the unique physical properties of deuterium and hydrogen, in chemical reactions or biological processes, deuterium atom traces can be detected to clarify the reaction mechanism, material transfer and metabolic pathways. For example, in the study of metabolism in organisms, specific biomolecules can be tagged with them, and tracked by precise analysis methods to gain insight into the mysteries of microscopic biochemical processes in organisms.
What are the physical properties of 1,3-dichloro-2-fluoro-5- (trifluoromethyl) benzene?
1% 2C3-dideuterium-2-deuterium-5- (trideuterium methyl) benzene is an organic compound. Its physical properties are as follows:
- ** Appearance and Properties **: Under normal temperature and pressure, it is mostly a colorless and transparent liquid. When pure, the visual perception is clear.
- ** Melting Boiling Point **: The melting point is low, and it begins to condense into a solid state at a certain low temperature; the boiling point varies according to external pressure. Under standard atmospheric pressure, its boiling point is in a specific temperature range, which makes it possible to realize the transformation of gas-liquid two phases under specific conditions.
- ** Density **: Compared with water, its density may be different. Due to the presence of deuterium atoms in the molecular composition, its mass is different from that of similar compounds composed of ordinary hydrogen, resulting in different densities.
- ** Solubility **: In organic solvents, such as some common hydrocarbons and ether solvents, or show good solubility and can dissolve with them to form a uniform mixture; however, in water, due to the characteristics of molecular structure, solubility or poor, it may be in a layered state with water.
- ** Volatility **: With a certain volatility, in an open environment, molecules easily escape from the liquid surface to the gas phase, and their volatilization rate is affected by factors such as temperature, surface area, and air circulation.
- ** Odor **: Or has a special smell, but the description of this smell requires professional olfactory perception and comparison, and the feeling may be slightly different due to individual olfactory differences.
- ** Appearance and Properties **: Under normal temperature and pressure, it is mostly a colorless and transparent liquid. When pure, the visual perception is clear.
- ** Melting Boiling Point **: The melting point is low, and it begins to condense into a solid state at a certain low temperature; the boiling point varies according to external pressure. Under standard atmospheric pressure, its boiling point is in a specific temperature range, which makes it possible to realize the transformation of gas-liquid two phases under specific conditions.
- ** Density **: Compared with water, its density may be different. Due to the presence of deuterium atoms in the molecular composition, its mass is different from that of similar compounds composed of ordinary hydrogen, resulting in different densities.
- ** Solubility **: In organic solvents, such as some common hydrocarbons and ether solvents, or show good solubility and can dissolve with them to form a uniform mixture; however, in water, due to the characteristics of molecular structure, solubility or poor, it may be in a layered state with water.
- ** Volatility **: With a certain volatility, in an open environment, molecules easily escape from the liquid surface to the gas phase, and their volatilization rate is affected by factors such as temperature, surface area, and air circulation.
- ** Odor **: Or has a special smell, but the description of this smell requires professional olfactory perception and comparison, and the feeling may be slightly different due to individual olfactory differences.
What are the chemical properties of 1,3-dichloro-2-fluoro-5- (trifluoromethyl) benzene?
1% 2C3-dioxy-2-pentene-5- (triamyl) naphthalene is one of the organic compounds. The chemical properties of this compound are quite unique and have multiple characteristics.
In its structure, the 1% 2C3-dioxy part makes the molecular electron cloud distribution unusual, giving it a certain polarity. This polarity causes the compound to exhibit special solubility in specific solvents. In polar solvents, its solubility is increased due to the principle of similar miscibility; in non-polar solvents, its solubility is limited.
2-pentene structure makes the molecule unsaturated. This unsaturated bond endows the compound with active chemical activity and can participate in a variety of addition reactions. For example, when it encounters halogen elements, such as bromine water, bromine atoms can be added to the double bond, causing the color of bromine water to fade, which is a typical reaction characteristic of olefins.
As for the 5- (triamyl) naphthalene part, the naphthalene ring is a fused ring aromatic hydrocarbon structure with certain stability and conjugation effect. The substitution of triamyl groups adds spatial hindrance and hydrophobicity to the molecule. The existence of spatial hindrance affects the difficulty of attack by other reagents when the compound participates in the reaction; hydrophobicity makes it tend to aggregate and separate from hydrophilic substances in the aqueous solution system.
Furthermore, due to the mutual influence of the structure of each part of the molecule, electronic effects are also reflected. The electron push or electron pull effect may occur between the conjugated system and the substituent, which in turn affects the electron cloud density and reactivity check point of the molecule as a whole. These complex structures and interactions have resulted in the unique chemical properties of 1% 2C3-dioxy-2-pentene-5- (triamyl) naphthalene, which may have potential application value in organic synthesis, materials science and other fields.
In its structure, the 1% 2C3-dioxy part makes the molecular electron cloud distribution unusual, giving it a certain polarity. This polarity causes the compound to exhibit special solubility in specific solvents. In polar solvents, its solubility is increased due to the principle of similar miscibility; in non-polar solvents, its solubility is limited.
2-pentene structure makes the molecule unsaturated. This unsaturated bond endows the compound with active chemical activity and can participate in a variety of addition reactions. For example, when it encounters halogen elements, such as bromine water, bromine atoms can be added to the double bond, causing the color of bromine water to fade, which is a typical reaction characteristic of olefins.
As for the 5- (triamyl) naphthalene part, the naphthalene ring is a fused ring aromatic hydrocarbon structure with certain stability and conjugation effect. The substitution of triamyl groups adds spatial hindrance and hydrophobicity to the molecule. The existence of spatial hindrance affects the difficulty of attack by other reagents when the compound participates in the reaction; hydrophobicity makes it tend to aggregate and separate from hydrophilic substances in the aqueous solution system.
Furthermore, due to the mutual influence of the structure of each part of the molecule, electronic effects are also reflected. The electron push or electron pull effect may occur between the conjugated system and the substituent, which in turn affects the electron cloud density and reactivity check point of the molecule as a whole. These complex structures and interactions have resulted in the unique chemical properties of 1% 2C3-dioxy-2-pentene-5- (triamyl) naphthalene, which may have potential application value in organic synthesis, materials science and other fields.
What is the production method of 1,3-dichloro-2-fluoro-5- (trifluoromethyl) benzene?
The preparation method of 1% 2C3-dioxo-2-pentene-5- (triamyl) benzene is an important matter in the field of chemical synthesis. To make this substance, you can follow the following steps:
Take an appropriate amount of starting material first, and weigh it carefully. This is the foundation for the successful synthesis. The selection of raw materials must be pure, impurities or cause reaction errors. The starting materials involved should be carefully selected according to the reaction mechanism, or a compound with a specific functional group, which lays the foundation for the subsequent reaction.
Reaction steps should be carried out in a suitable reaction vessel. Or in a flask, add raw materials and specific catalysts in sequence. The choice of catalyst is extremely critical, which can change the rate of chemical reaction and make the reaction proceed efficiently. Depending on the reaction characteristics, temperature control and pressure control may be required. Heating up or using heating jackets, oil baths and other devices to precisely control the temperature, or at a specific temperature range, to ensure that the reaction proceeds according to the established path. Pressurization also requires special equipment to make the reaction environment meet the requirements.
During the reaction, the reaction process needs to be closely monitored. Analytical methods such as thin-layer chromatography and liquid chromatography can be used to gain insight into the degree of reaction progress. Observe the consumption of reactants and product formation. If the reaction does not meet expectations, the reaction conditions may need to be adjusted, such as increasing or decreasing the amount of catalyst, fine-tuning temperature and pressure.
When the reaction reaches the expected degree, the product is separated and purified This step is also crucial, because the reaction product or mixed with impurities. Distillation, extraction, recrystallization and other methods can be used. Distillation is separated according to the difference in boiling point of the substance, extraction is extracted by different solubility of the solute in different solvents, and recrystallization makes the product recrystallized in a suitable solvent to achieve the effect of purification. After these steps, high purity 1% 2C3-dioxo-2-pentene-5 - (triamyl) benzene can be obtained. The whole preparation process requires careful operation by the experimenter and strict adherence to the specifications to ensure the successful synthesis.
Take an appropriate amount of starting material first, and weigh it carefully. This is the foundation for the successful synthesis. The selection of raw materials must be pure, impurities or cause reaction errors. The starting materials involved should be carefully selected according to the reaction mechanism, or a compound with a specific functional group, which lays the foundation for the subsequent reaction.
Reaction steps should be carried out in a suitable reaction vessel. Or in a flask, add raw materials and specific catalysts in sequence. The choice of catalyst is extremely critical, which can change the rate of chemical reaction and make the reaction proceed efficiently. Depending on the reaction characteristics, temperature control and pressure control may be required. Heating up or using heating jackets, oil baths and other devices to precisely control the temperature, or at a specific temperature range, to ensure that the reaction proceeds according to the established path. Pressurization also requires special equipment to make the reaction environment meet the requirements.
During the reaction, the reaction process needs to be closely monitored. Analytical methods such as thin-layer chromatography and liquid chromatography can be used to gain insight into the degree of reaction progress. Observe the consumption of reactants and product formation. If the reaction does not meet expectations, the reaction conditions may need to be adjusted, such as increasing or decreasing the amount of catalyst, fine-tuning temperature and pressure.
When the reaction reaches the expected degree, the product is separated and purified This step is also crucial, because the reaction product or mixed with impurities. Distillation, extraction, recrystallization and other methods can be used. Distillation is separated according to the difference in boiling point of the substance, extraction is extracted by different solubility of the solute in different solvents, and recrystallization makes the product recrystallized in a suitable solvent to achieve the effect of purification. After these steps, high purity 1% 2C3-dioxo-2-pentene-5 - (triamyl) benzene can be obtained. The whole preparation process requires careful operation by the experimenter and strict adherence to the specifications to ensure the successful synthesis.
What are the precautions for using 1,3-dichloro-2-fluoro-5- (trifluoromethyl) benzene?
1% 2C3-dihydro-2-pentyl-5- (triamyl) naphthalene should pay attention to the following things during use:
First, it is related to storage. Because of its nature or more active, it should be placed in a cool, dry and well-ventilated place, away from fire and heat sources. If the storage environment is not good, such as high temperature or excessive humidity, it may cause the material to deteriorate, affecting its performance and use effect.
Second, about operation. Be sure to strictly follow the established procedures when operating. Because its chemical structure has a specific activity, improper operation or danger. When taking it, a precise measuring tool should be used to ensure accurate dosage and avoid abnormal subsequent reactions due to dosage deviations. At the same time, the operating environment should be neat and orderly to prevent impurities from mixing in and interfering with its chemical properties.
Third, safety protection is involved. This substance may be toxic and irritating to a certain extent, and the operator must take protective measures. Appropriate protective gloves should be worn to avoid direct contact with the skin to prevent skin allergies, burns, etc. Protective glasses and masks should also be worn to prevent substances from splashing into the eyes or being inhaled into the respiratory tract, causing damage to the body.
Fourth, pay attention to the reaction conditions. When participating in chemical reactions, strict requirements are required for the reaction conditions. Factors such as temperature, pressure, and reaction time all have a significant impact on the reaction process and products. If the temperature is too high or too low, or the reaction rate is too fast or too slow, or even the reaction cannot be carried out. Therefore, it is necessary to precisely control the reaction conditions to ensure that the reaction successfully achieves the desired goal.
First, it is related to storage. Because of its nature or more active, it should be placed in a cool, dry and well-ventilated place, away from fire and heat sources. If the storage environment is not good, such as high temperature or excessive humidity, it may cause the material to deteriorate, affecting its performance and use effect.
Second, about operation. Be sure to strictly follow the established procedures when operating. Because its chemical structure has a specific activity, improper operation or danger. When taking it, a precise measuring tool should be used to ensure accurate dosage and avoid abnormal subsequent reactions due to dosage deviations. At the same time, the operating environment should be neat and orderly to prevent impurities from mixing in and interfering with its chemical properties.
Third, safety protection is involved. This substance may be toxic and irritating to a certain extent, and the operator must take protective measures. Appropriate protective gloves should be worn to avoid direct contact with the skin to prevent skin allergies, burns, etc. Protective glasses and masks should also be worn to prevent substances from splashing into the eyes or being inhaled into the respiratory tract, causing damage to the body.
Fourth, pay attention to the reaction conditions. When participating in chemical reactions, strict requirements are required for the reaction conditions. Factors such as temperature, pressure, and reaction time all have a significant impact on the reaction process and products. If the temperature is too high or too low, or the reaction rate is too fast or too slow, or even the reaction cannot be carried out. Therefore, it is necessary to precisely control the reaction conditions to ensure that the reaction successfully achieves the desired goal.
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