Linshang Chemical
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Benzene, 1-Chloro-4-Isocyanato-2-(Trifluoromethyl)-
Linshang Chemical
|
HS Code |
746166 |
| Chemical Formula | C8H3ClF3NO |
| Molecular Weight | 221.56 |
| Appearance | Typically a colorless to pale - yellow liquid |
| Boiling Point | Data may vary, around a specific value based on purity and conditions |
| Density | Determined experimentally with a specific value |
| Vapor Pressure | Depends on temperature, with a given value at a certain T |
| Solubility | Soluble in some organic solvents like dichloromethane |
| Flash Point | Has a defined flash point value |
| Stability | Can be stable under normal conditions but reactive with certain substances |
As an accredited Benzene, 1-Chloro-4-Isocyanato-2-(Trifluoromethyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 1 - chloro - 4 - isocyanato - 2 - (trifluoromethyl) benzene in sealed chemical - grade bottles. |
| Storage | **Storage for 1 - chloro - 4 - isocyanato - 2 - (trifluoromethyl)benzene**: Store this chemical in a cool, well - ventilated area, away from heat, sparks, and open flames as it may be flammable. Keep it in a tightly sealed container to prevent leakage and exposure to air and moisture, which could lead to reactions. Isolate it from incompatible substances like amines, alcohols, and strong acids. Use dedicated storage cabinets and follow all safety regulations. |
| Shipping | 1 - Chloro - 4 - isocyanato - 2 - (trifluoromethyl) benzene is a hazardous chemical. It must be shipped in accordance with strict regulations, using proper packaging to prevent leaks, and labeled clearly to indicate its dangerous nature. |
Competitive Benzene, 1-Chloro-4-Isocyanato-2-(Trifluoromethyl)- prices that fit your budget—flexible terms and customized quotes for every order.
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What is the main use of this product 1-chloro-4-isocyanate-2- (trifluoromethyl) benzene
The substance is called 1-chloro-4-isobutyryl-2 - (triethylamino) naphthalene, and its main uses are as follows:
This is a class of compounds that are crucial in the field of medicine and organic synthesis. In the field of medicine, because of its unique chemical structure and activity, it may act as a key intermediate for the preparation of drugs with specific physiological activities. By modifying and modifying its structure, therapeutic drugs for specific diseases can be developed, such as some anti-cancer drugs and antiviral drugs with unique pharmacological effects. Cover because of its chemical structure, each part may interact with specific targets in organisms to play a role in regulating physiological functions.
In the field of organic synthesis, it is often used as a basic module for the construction of more complex organic molecules. With its chlorine atom, isobutyryl group and triethylamino naphthalene structure, it can be combined with other organic reagents through many organic reactions, such as nucleophilic substitution reaction, acylation reaction, etc., to form carbon-carbon bonds, carbon-heteroatomic bonds, etc., and then synthesize organic compounds with novel structures and unique functions. These compounds may have unique application value in the fields of materials science, fine chemistry, etc., such as as synthetic precursors of new optoelectronic materials, laying the foundation for the development of high-performance optoelectronic devices. In short, this compound is an important basic substance in many fields, and is of great significance to promote the development of related fields.
This is a class of compounds that are crucial in the field of medicine and organic synthesis. In the field of medicine, because of its unique chemical structure and activity, it may act as a key intermediate for the preparation of drugs with specific physiological activities. By modifying and modifying its structure, therapeutic drugs for specific diseases can be developed, such as some anti-cancer drugs and antiviral drugs with unique pharmacological effects. Cover because of its chemical structure, each part may interact with specific targets in organisms to play a role in regulating physiological functions.
In the field of organic synthesis, it is often used as a basic module for the construction of more complex organic molecules. With its chlorine atom, isobutyryl group and triethylamino naphthalene structure, it can be combined with other organic reagents through many organic reactions, such as nucleophilic substitution reaction, acylation reaction, etc., to form carbon-carbon bonds, carbon-heteroatomic bonds, etc., and then synthesize organic compounds with novel structures and unique functions. These compounds may have unique application value in the fields of materials science, fine chemistry, etc., such as as synthetic precursors of new optoelectronic materials, laying the foundation for the development of high-performance optoelectronic devices. In short, this compound is an important basic substance in many fields, and is of great significance to promote the development of related fields.
What are the physical properties of 1-chloro-4-isocyanate-2- (trifluoromethyl) benzene
1 + -Alkane-4-isovalerate-2- (triethylmethyl) iridium is a chemical substance, and its physical properties are quite specific.
In this compound, numbers such as 1, 2, and 4 are important for each epitope and structure. The alkane is the basic hydrocarbon skeleton, with the characteristics of alkanes. Its carbon-carbon single bond is relatively stable and saturated, and its chemical activity is relatively gentle at room temperature and pressure. Isovalerate, on the other hand, contains a change of carboxyl group, which gives it a certain polarity. Carboxyl groups can participate in many reactions, such as ester formation and salt formation.
In addition, (triethylmethyl) iridium part, iridium is a transition metal with empty orbit, which can form coordination bonds with ligands such as isovalerate. Triethylmethyl surrounds iridium atoms and affects the distribution of its electron cloud. This structure results in the unique solubility of the compound, which is different in polar and non-polar solvents. In some organic solvents, such as benzene and toluene, the alkane skeleton and triethylmethyl may have a certain solubility due to the non-polarity; in water, the solubility may be low due to the limited polarity of the whole.
Its melting point and boiling point are also affected by the structure. The intermolecular forces include van der Waals forces. Due to the large size of the molecule and the complex structure, the van der Waals forces are relatively considerable, which may cause its melting point and boiling point to be higher than that of some simple alkanes. And the existence of the transition metal iridium makes the compound have certain thermal stability. In a specific temperature range, the structure can be stable and not easily decomposed.
In addition, the density of the compound is also related to the structure. Many atoms and groups are aggregated, resulting in different mass per unit volume. Overall, this 1 + -alkane-4-isovalerate-2 - (triethylmethyl) iridium exhibits a series of specific physical properties such as melting point, boiling point, solubility, and density due to its unique chemical structure.
In this compound, numbers such as 1, 2, and 4 are important for each epitope and structure. The alkane is the basic hydrocarbon skeleton, with the characteristics of alkanes. Its carbon-carbon single bond is relatively stable and saturated, and its chemical activity is relatively gentle at room temperature and pressure. Isovalerate, on the other hand, contains a change of carboxyl group, which gives it a certain polarity. Carboxyl groups can participate in many reactions, such as ester formation and salt formation.
In addition, (triethylmethyl) iridium part, iridium is a transition metal with empty orbit, which can form coordination bonds with ligands such as isovalerate. Triethylmethyl surrounds iridium atoms and affects the distribution of its electron cloud. This structure results in the unique solubility of the compound, which is different in polar and non-polar solvents. In some organic solvents, such as benzene and toluene, the alkane skeleton and triethylmethyl may have a certain solubility due to the non-polarity; in water, the solubility may be low due to the limited polarity of the whole.
Its melting point and boiling point are also affected by the structure. The intermolecular forces include van der Waals forces. Due to the large size of the molecule and the complex structure, the van der Waals forces are relatively considerable, which may cause its melting point and boiling point to be higher than that of some simple alkanes. And the existence of the transition metal iridium makes the compound have certain thermal stability. In a specific temperature range, the structure can be stable and not easily decomposed.
In addition, the density of the compound is also related to the structure. Many atoms and groups are aggregated, resulting in different mass per unit volume. Overall, this 1 + -alkane-4-isovalerate-2 - (triethylmethyl) iridium exhibits a series of specific physical properties such as melting point, boiling point, solubility, and density due to its unique chemical structure.
What are the chemical properties of 1-chloro-4-isocyanate-2- (trifluoromethyl) benzene
1 + -Alkane-4-isovalerate-2- (triethylmethyl) osmium, this compound has unique chemical properties.
Its metal center, osmium, exhibits typical characteristics of transition metals due to its specific coordination environment. In terms of oxidation state, osmium can exhibit multiple valence states, which are stable in the complex, which makes the compound play a special role in some redox reactions. In case of strong oxidants, the valence state of osmium may increase, triggering ligand structure adjustment; in case of strong reducing agents, the valence state may decrease, changing the electron cloud distribution of the complex.
From the perspective of coordination structure, ligands such as isovalerate and triethylmethyl are arranged around osmium atoms in a specific geometric configuration. This spatial structure endows the compound with specific physical and chemical properties. The ligand steric hindrance affects its reactivity. The large steric hindrance ligand or restricts the reactant from being close to the metal center, reduces the reaction rate, or selectively promotes the reaction in some specific directions. It can be used as a catalyst in organic synthesis reactions to selectively generate products of specific configurations using its spatial structure.
Furthermore, elements such as hydrocarbons in the compound constitute the organic ligand part, endowing it with certain solubility and affinity. Due to the existence of organic ligands, the solubility of the compound in organic solvents is better than in water, which is of great significance in separation and purification or selection of reaction systems. In the organic phase reaction system, it can be more uniformly dispersed and improve the reaction efficiency.
In addition, the chemical bonds in this compound are subtle. The chemical bonds between metals and ligands have both ionic bond characteristics and covalent bond components. This mixed bond type affects its stability and reactivity. The strength of the chemical bond determines the stability of the compound under different conditions. When exposed to heat, light or chemical reagents, the chemical bonds may break and recombine, triggering the decomposition or transformation of the compound.
Its metal center, osmium, exhibits typical characteristics of transition metals due to its specific coordination environment. In terms of oxidation state, osmium can exhibit multiple valence states, which are stable in the complex, which makes the compound play a special role in some redox reactions. In case of strong oxidants, the valence state of osmium may increase, triggering ligand structure adjustment; in case of strong reducing agents, the valence state may decrease, changing the electron cloud distribution of the complex.
From the perspective of coordination structure, ligands such as isovalerate and triethylmethyl are arranged around osmium atoms in a specific geometric configuration. This spatial structure endows the compound with specific physical and chemical properties. The ligand steric hindrance affects its reactivity. The large steric hindrance ligand or restricts the reactant from being close to the metal center, reduces the reaction rate, or selectively promotes the reaction in some specific directions. It can be used as a catalyst in organic synthesis reactions to selectively generate products of specific configurations using its spatial structure.
Furthermore, elements such as hydrocarbons in the compound constitute the organic ligand part, endowing it with certain solubility and affinity. Due to the existence of organic ligands, the solubility of the compound in organic solvents is better than in water, which is of great significance in separation and purification or selection of reaction systems. In the organic phase reaction system, it can be more uniformly dispersed and improve the reaction efficiency.
In addition, the chemical bonds in this compound are subtle. The chemical bonds between metals and ligands have both ionic bond characteristics and covalent bond components. This mixed bond type affects its stability and reactivity. The strength of the chemical bond determines the stability of the compound under different conditions. When exposed to heat, light or chemical reagents, the chemical bonds may break and recombine, triggering the decomposition or transformation of the compound.
What is the production method of 1-chloro-4-isocyanate-2- (trifluoromethyl) benzene?
To prepare 1-bromo-4-isobromate 2 - (triethyl) benzene, the method is as follows:
First take an appropriate amount of raw materials and put them in a clean vessel. First prepare the various reagents required for the reaction in the appropriate proportion, which is the basis for the successful reaction.
In the reactor, place a substrate containing benzene ring, which should be carefully purified to ensure the purity and efficiency of the reaction. Then slowly inject a specific brominating reagent, which needs to have good reactivity, and when added, the rate should be controlled to maintain the stability of the reaction system. In the process of adding brominated reagents, it is necessary to pay close attention to the reaction temperature and reaction phenomenon. If the temperature is too high or too low, it may affect the reaction process, resulting in impure products or low yields.
At the same time, a suitable catalyst needs to be added, which can effectively accelerate the reaction rate and reduce the activation energy required for the reaction. The amount of catalyst needs to be precisely controlled, and too much or too little is not conducive to the reaction.
During the reaction process, it is necessary to continuously stir to make the reactants fully contact and promote the uniform occurrence of the reaction. When the reaction is carried out to a certain extent, the reaction process can be monitored by suitable detection methods, such as chromatographic analysis, to determine whether the reaction is completed. After the
reaction is completed, the product is separated and purified. First, the extraction method is used to preliminarily separate the product by taking advantage of the difference in solubility of the product and impurities in different solvents. Then the product is further purified through distillation, recrystallization and other steps to obtain high-purity 1-bromo-4-isobromate 2- (triethylmethyl) benzene. The whole process requires rigorous operation and attention to detail to obtain high-quality products.
First take an appropriate amount of raw materials and put them in a clean vessel. First prepare the various reagents required for the reaction in the appropriate proportion, which is the basis for the successful reaction.
In the reactor, place a substrate containing benzene ring, which should be carefully purified to ensure the purity and efficiency of the reaction. Then slowly inject a specific brominating reagent, which needs to have good reactivity, and when added, the rate should be controlled to maintain the stability of the reaction system. In the process of adding brominated reagents, it is necessary to pay close attention to the reaction temperature and reaction phenomenon. If the temperature is too high or too low, it may affect the reaction process, resulting in impure products or low yields.
At the same time, a suitable catalyst needs to be added, which can effectively accelerate the reaction rate and reduce the activation energy required for the reaction. The amount of catalyst needs to be precisely controlled, and too much or too little is not conducive to the reaction.
During the reaction process, it is necessary to continuously stir to make the reactants fully contact and promote the uniform occurrence of the reaction. When the reaction is carried out to a certain extent, the reaction process can be monitored by suitable detection methods, such as chromatographic analysis, to determine whether the reaction is completed. After the
reaction is completed, the product is separated and purified. First, the extraction method is used to preliminarily separate the product by taking advantage of the difference in solubility of the product and impurities in different solvents. Then the product is further purified through distillation, recrystallization and other steps to obtain high-purity 1-bromo-4-isobromate 2- (triethylmethyl) benzene. The whole process requires rigorous operation and attention to detail to obtain high-quality products.
What are the precautions for the use of 1-chloro-4-isocyanate-2- (trifluoromethyl) benzene?
1 + -Alkane-4-isoalkanoate-2- (triethylmethyl) tin This substance should pay attention to many matters during use.
First, this compound contains tin, and tin and its compounds are mostly toxic. During operation, be sure to avoid direct contact with the skin. If it is accidentally touched, it should be washed with a lot of water immediately. If the contact area is large or uncomfortable, seek medical attention immediately. Do not inhale its dust or volatile gases. It should be operated in a well-ventilated place or with the help of ventilation equipment to prevent damage to the body due to inhalation.
Second, its chemical properties are sensitive to acid-base environments due to structures such as isoalkanoate. When exposed to strong acids and alkalis, or cause chemical reactions, resulting in structural changes and performance damage. Therefore, when storing and using, keep away from strong acids and alkalis. At the same time, as an organometallic compound, under certain conditions or with a certain degree of oxidation or reduction, when co-located with other redox substances, caution should be taken to prevent adverse reactions.
Third, from the perspective of storage, it should be placed in a cool, dry and well-ventilated place. Avoid direct sunlight, because light may accelerate its decomposition or cause other photochemical reactions. And it should be stored separately from other chemicals, especially those substances that may react with it, classified and marked for easy management and access to prevent misuse.
Fourth, when using, the relevant operators need to be professionally trained to be familiar with its nature, hazards and operating specifications. Operate strictly according to the established process, and do not change the steps or increase or decrease the dosage without authorization. During the experiment or production process, protective measures should be taken, such as wearing protective gloves, goggles, masks, etc., to ensure personal safety.
First, this compound contains tin, and tin and its compounds are mostly toxic. During operation, be sure to avoid direct contact with the skin. If it is accidentally touched, it should be washed with a lot of water immediately. If the contact area is large or uncomfortable, seek medical attention immediately. Do not inhale its dust or volatile gases. It should be operated in a well-ventilated place or with the help of ventilation equipment to prevent damage to the body due to inhalation.
Second, its chemical properties are sensitive to acid-base environments due to structures such as isoalkanoate. When exposed to strong acids and alkalis, or cause chemical reactions, resulting in structural changes and performance damage. Therefore, when storing and using, keep away from strong acids and alkalis. At the same time, as an organometallic compound, under certain conditions or with a certain degree of oxidation or reduction, when co-located with other redox substances, caution should be taken to prevent adverse reactions.
Third, from the perspective of storage, it should be placed in a cool, dry and well-ventilated place. Avoid direct sunlight, because light may accelerate its decomposition or cause other photochemical reactions. And it should be stored separately from other chemicals, especially those substances that may react with it, classified and marked for easy management and access to prevent misuse.
Fourth, when using, the relevant operators need to be professionally trained to be familiar with its nature, hazards and operating specifications. Operate strictly according to the established process, and do not change the steps or increase or decrease the dosage without authorization. During the experiment or production process, protective measures should be taken, such as wearing protective gloves, goggles, masks, etc., to ensure personal safety.
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