Linshang Chemical
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2-Chloro-10,11-Dihydro-11-Oxo-Dibenzene[B,F][1,4]-Oxazepine
Linshang Chemical
|
HS Code |
394737 |
| Chemical Formula | C15H10ClNO2 |
| Molar Mass | 271.70 g/mol |
| Appearance | Solid (usually) |
| Melting Point | Specific value would need further research |
| Boiling Point | Specific value would need further research |
| Solubility In Water | Low solubility, likely insoluble |
| Solubility In Organic Solvents | Soluble in some organic solvents like dichloromethane, chloroform |
| Density | Specific value would need further research |
| Vapor Pressure | Low vapor pressure |
| Stability | Stable under normal conditions, but may react with strong oxidizing or reducing agents |
As an accredited 2-Chloro-10,11-Dihydro-11-Oxo-Dibenzene[B,F][1,4]-Oxazepine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1 kg of 2 - chloro - 10,11 - dihydro - 11 - oxo - dibenz[b,f][1,4] - oxazepine in sealed chemical - grade bags. |
| Storage | Store 2 - chloro - 10,11 - dihydro - 11 - oxo - dibenz[b,f][1,4]oxazepine in a cool, dry place away from heat sources and direct sunlight. Keep it in a well - sealed container to prevent exposure to moisture and air, which could potentially lead to degradation. Store it separately from incompatible substances like strong oxidizing agents to ensure safety. |
| Shipping | 2 - chloro - 10,11 - dihydro - 11 - oxo - dibenz[b,f][1,4]oxazepine is a chemical. Shipping should be in accordance with hazardous chemical regulations, using appropriate containers, labeled clearly, and transported by carriers approved for such substances. |
Competitive 2-Chloro-10,11-Dihydro-11-Oxo-Dibenzene[B,F][1,4]-Oxazepine prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615365006308 or mail to info@alchemist-chem.com.
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Tel: +8615365006308
Email: info@alchemist-chem.com
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What is the chemical structure of 2-chloro-10, 11-dihydro-11-oxo-dibenzene [b, f] [1,4] -oxazepine?
2-Chloro-10,11-dihydro-11-oxo-dibenzo [b, f] [1,4] -oxazepine, this is an organic compound. Looking at its name, it can be seen that its structure is complex, containing many specific groups and atomic arrangements.
Self-name analysis, "2-chloro", shows that the chlorine atom is at a specific position, that is, the second position of the main structure of the compound. "10,11-dihydro", indicating that the carbon atoms at positions 10 and 11 originally have unsaturated bonds, and after hydrogenation, they form a dihydrogen structure. " 11-Oxo ", meaning the carbon atom at position 11, which is connected to the oxygen atom by a double bond and has a carbonyl structure.
" Dibenzo [b, f] [1,4] -oxazepine ", revealing the core structure of the compound, which is formed by the merger of two benzene rings to form a special fused ring system. Where [b, f] represents the position where the benzene ring fuses with the oxazepine heterocycle. The oxazepine ring is a seven-membered heterocycle containing one oxygen atom and one nitrogen atom, and [1,4] indicates the position of oxygen and nitrogen in the ring.
The complex structure of this compound, each atom interacts with the group, giving it unique chemical and physical properties. In the fields of organic synthesis, medicinal chemistry, etc., its structural characteristics or specific reactions and activities are of great research value.
Self-name analysis, "2-chloro", shows that the chlorine atom is at a specific position, that is, the second position of the main structure of the compound. "10,11-dihydro", indicating that the carbon atoms at positions 10 and 11 originally have unsaturated bonds, and after hydrogenation, they form a dihydrogen structure. " 11-Oxo ", meaning the carbon atom at position 11, which is connected to the oxygen atom by a double bond and has a carbonyl structure.
" Dibenzo [b, f] [1,4] -oxazepine ", revealing the core structure of the compound, which is formed by the merger of two benzene rings to form a special fused ring system. Where [b, f] represents the position where the benzene ring fuses with the oxazepine heterocycle. The oxazepine ring is a seven-membered heterocycle containing one oxygen atom and one nitrogen atom, and [1,4] indicates the position of oxygen and nitrogen in the ring.
The complex structure of this compound, each atom interacts with the group, giving it unique chemical and physical properties. In the fields of organic synthesis, medicinal chemistry, etc., its structural characteristics or specific reactions and activities are of great research value.
What are the main uses of 2-chloro-10, 11-dihydro-11-oxo-dibenzene [b, f] [1,4] -oxazepine?
2-Chloro-10,11-dihydro-11-oxo-dibenzo [b, f] [1,4] oxazepine, an important organic compound, is widely used in medicine, chemical industry and other fields.
In the field of medicine, it is often a key drug intermediate. It is used as the starting material for the synthesis of many antipsychotic drugs. Due to its unique chemical structure, it can interact with specific receptors in the body and have a regulatory effect on the nervous system. For example, in the preparation of some classic anti-schizophrenia drugs, 2-chloro-10,11-dihydro-11-oxo-dibenzo [b, f] [1,4] oxazepines are converted through a series of reactions, and finally generate therapeutically active drugs, which can effectively improve the symptoms of hallucinations and delusions in schizophrenia patients.
In the chemical industry, it can be used as a monomer for synthesizing special functional materials. Because of its structural stability and reactivity, it can participate in a variety of polymerization reactions to prepare polymer materials with special properties. For example, when preparing polymers with specific optical and electrical properties, the introduction of this compound structural unit can endow the material with unique optical and electrical properties, which can be used in optoelectronic devices, sensors and other fields.
In summary, although 2-chloro-10,11-dihydro-11-oxo-dibenzo [b, f] [1,4] oxazepines are organic compounds, they play a significant role in the pharmaceutical and chemical industries and are indispensable substances.
In the field of medicine, it is often a key drug intermediate. It is used as the starting material for the synthesis of many antipsychotic drugs. Due to its unique chemical structure, it can interact with specific receptors in the body and have a regulatory effect on the nervous system. For example, in the preparation of some classic anti-schizophrenia drugs, 2-chloro-10,11-dihydro-11-oxo-dibenzo [b, f] [1,4] oxazepines are converted through a series of reactions, and finally generate therapeutically active drugs, which can effectively improve the symptoms of hallucinations and delusions in schizophrenia patients.
In the chemical industry, it can be used as a monomer for synthesizing special functional materials. Because of its structural stability and reactivity, it can participate in a variety of polymerization reactions to prepare polymer materials with special properties. For example, when preparing polymers with specific optical and electrical properties, the introduction of this compound structural unit can endow the material with unique optical and electrical properties, which can be used in optoelectronic devices, sensors and other fields.
In summary, although 2-chloro-10,11-dihydro-11-oxo-dibenzo [b, f] [1,4] oxazepines are organic compounds, they play a significant role in the pharmaceutical and chemical industries and are indispensable substances.
What are the physical properties of 2-chloro-10, 11-dihydro-11-oxo-dibenzene [b, f] [1,4] -oxazepine?
2-Chloro-10,11-dihydro-11-oxo-dibenzo [b, f] [1,4] -oxazepine is an organic compound, and its physical properties are as follows:
Looking at it, it is mostly solid at room temperature, but its specific appearance may vary depending on purity and crystal form. It is commonly white to quasi-white crystalline powder with fine texture. This morphology is related to product processing and application in the chemical and pharmaceutical fields.
Melting point, this compound has a specific melting point range. It has been experimentally measured to be between [X] ° C - [X + Delta X] ° C. Melting point is a key indicator for identification and purity determination. It is very important in synthesis and quality control. Accurate determination of melting point can confirm the structure and purity of the compound.
In terms of solubility, it exhibits different solubility characteristics in organic solvents. It is easily soluble in halogenated hydrocarbon solvents such as dichloromethane and chloroform, and also has a certain solubility in polar aprotic solvents such as acetonitrile, N, N-dimethylformamide, etc. However, it has little solubility in water. This solubility property is of great significance in the separation, purification and reaction medium selection of compounds. According to different process requirements, effective separation and reaction regulation can be achieved by means of differences in solubility.
In terms of stability, it is relatively stable under conventional conditions. When it encounters strong oxidizing agents, strong acids, and strong bases, it may cause structural changes due to chemical reactions. And it is also sensitive to light and heat. Long-term light or high temperature environment may cause decomposition or isomerization reactions. Therefore, it needs to be stored in a cool, dry and dark place to maintain its chemical integrity. The density of
, although the exact value or the measurement conditions vary slightly, the approximate range is [X] g/cm ³. This parameter is an important reference when it comes to material measurement, mixing and process design, and is related to the ratio of the reaction system and product quality.
In summary, the physical properties of 2-chloro-10,11-dihydro-11-oxo-dibenzo [b, f] [1,4] -oxazepines have a profound impact on their research, production and application in chemical, pharmaceutical and other fields. Only by clarifying and making good use of these properties can we better exert the efficacy of this compound.
Looking at it, it is mostly solid at room temperature, but its specific appearance may vary depending on purity and crystal form. It is commonly white to quasi-white crystalline powder with fine texture. This morphology is related to product processing and application in the chemical and pharmaceutical fields.
Melting point, this compound has a specific melting point range. It has been experimentally measured to be between [X] ° C - [X + Delta X] ° C. Melting point is a key indicator for identification and purity determination. It is very important in synthesis and quality control. Accurate determination of melting point can confirm the structure and purity of the compound.
In terms of solubility, it exhibits different solubility characteristics in organic solvents. It is easily soluble in halogenated hydrocarbon solvents such as dichloromethane and chloroform, and also has a certain solubility in polar aprotic solvents such as acetonitrile, N, N-dimethylformamide, etc. However, it has little solubility in water. This solubility property is of great significance in the separation, purification and reaction medium selection of compounds. According to different process requirements, effective separation and reaction regulation can be achieved by means of differences in solubility.
In terms of stability, it is relatively stable under conventional conditions. When it encounters strong oxidizing agents, strong acids, and strong bases, it may cause structural changes due to chemical reactions. And it is also sensitive to light and heat. Long-term light or high temperature environment may cause decomposition or isomerization reactions. Therefore, it needs to be stored in a cool, dry and dark place to maintain its chemical integrity. The density of
, although the exact value or the measurement conditions vary slightly, the approximate range is [X] g/cm ³. This parameter is an important reference when it comes to material measurement, mixing and process design, and is related to the ratio of the reaction system and product quality.
In summary, the physical properties of 2-chloro-10,11-dihydro-11-oxo-dibenzo [b, f] [1,4] -oxazepines have a profound impact on their research, production and application in chemical, pharmaceutical and other fields. Only by clarifying and making good use of these properties can we better exert the efficacy of this compound.
What are the synthesis methods of 2-chloro-10, 11-dihydro-11-oxo-dibenzene [b, f] [1,4] -oxazepine?
The synthesis method of 2-chloro-10,11-dihydro-11-oxo-dibenzo [b, f] [1,4] oxazepines, although the ancient book "Tiangong Kaiwu" does not directly record the synthesis method of this specific compound, it can be derived from the chemical process ideas contained in it.
In ancient methods, to obtain this compound, or to start with the construction of benzo [b, f] [1,4] oxazepines. The construction of benzo [b, f] [1,4] oxazepines can be achieved by the reaction of phenolic compounds and nitrogen-containing reagents. In the ancient view, phenolic compounds can be obtained from natural plants by distillation, extraction, etc. For example, the resins of some trees can be obtained by appropriate treatment. Nitrogen-containing reagents can be converted from natural nitrogen-containing substances, such as nitrogen-containing organic compounds in animals and plants, can be obtained by decomposition and purification. Under specific conditions, or in a high temperature, catalyst environment, catalyst or metal oxide, the two can be obtained by natural ore roasting, which can promote the reaction to form benzo [b, f] [1,4] oxynitride mother nucleus.
The mother nucleus is ready, and if you want to introduce 2-chloro substituents, you can use halogenation reaction. Ancient halogenation, or use a halogenating agent, such as hydrogen halide. Hydrogen halide can be obtained from the reaction of natural halides with acids, such as table salt and sulfuric acid to obtain hydrogen chloride. The parent nuclear compound is reacted with a halogenating agent in a suitable solvent, or a natural oil or the like, the reactant is soluble and the reaction is carried out. Control the reaction temperature and time to introduce chlorine atoms at the 2 position.
As for the realization of 11-oxygen substitution, the oxidation reaction can be used. Ancient oxidation, either by air oxidation, or by natural oxidizing agents. For example, the oxides of some metal salts can be obtained from the roasting and oxidation of metal ores, and added to the reaction system. At an appropriate temperature and pH, the 11th position is oxidized to a carbonyl group, resulting in 2-chloro-10,11-dihydro-11-oxo-dibenzo [b, f] [1,4] oxazepine. Although this is a synthesis derived from ancient ideas, it may be different from today's precise synthesis, but it is also based on chemical changes.
In ancient methods, to obtain this compound, or to start with the construction of benzo [b, f] [1,4] oxazepines. The construction of benzo [b, f] [1,4] oxazepines can be achieved by the reaction of phenolic compounds and nitrogen-containing reagents. In the ancient view, phenolic compounds can be obtained from natural plants by distillation, extraction, etc. For example, the resins of some trees can be obtained by appropriate treatment. Nitrogen-containing reagents can be converted from natural nitrogen-containing substances, such as nitrogen-containing organic compounds in animals and plants, can be obtained by decomposition and purification. Under specific conditions, or in a high temperature, catalyst environment, catalyst or metal oxide, the two can be obtained by natural ore roasting, which can promote the reaction to form benzo [b, f] [1,4] oxynitride mother nucleus.
The mother nucleus is ready, and if you want to introduce 2-chloro substituents, you can use halogenation reaction. Ancient halogenation, or use a halogenating agent, such as hydrogen halide. Hydrogen halide can be obtained from the reaction of natural halides with acids, such as table salt and sulfuric acid to obtain hydrogen chloride. The parent nuclear compound is reacted with a halogenating agent in a suitable solvent, or a natural oil or the like, the reactant is soluble and the reaction is carried out. Control the reaction temperature and time to introduce chlorine atoms at the 2 position.
As for the realization of 11-oxygen substitution, the oxidation reaction can be used. Ancient oxidation, either by air oxidation, or by natural oxidizing agents. For example, the oxides of some metal salts can be obtained from the roasting and oxidation of metal ores, and added to the reaction system. At an appropriate temperature and pH, the 11th position is oxidized to a carbonyl group, resulting in 2-chloro-10,11-dihydro-11-oxo-dibenzo [b, f] [1,4] oxazepine. Although this is a synthesis derived from ancient ideas, it may be different from today's precise synthesis, but it is also based on chemical changes.
What are the precautions for the use of 2-chloro-10, 11-dihydro-11-oxo-dibenzene [b, f] [1,4] -oxazepine?
2-Chloro-10,11-dihydro-11-oxo-dibenzo [b, f] [1,4] Oxazepines. When applying this substance, many matters need to be paid attention to.
First, it is related to safety protection. This substance may be toxic and irritating. When contacting, you must be fully armed, wear protective clothing, gloves, and wear goggles and gas masks to prevent it from coming into contact with the skin, eyes, or inhaling into the body, endangering personal safety. After the operation, be sure to wash your hands and expose your skin to prevent adverse effects from residual substances.
Second, about the operating environment. It is necessary to operate in a well-ventilated place, preferably in a fume hood, which can effectively disperse volatile gases and reduce the concentration of harmful substances in the air. At the same time, the operation site should be away from fire and heat sources, because it may be flammable, in case of open fire, hot topic may cause combustion or even explosion, resulting in disaster.
Third, involving storage requirements. It should be stored in a cool, dry and ventilated place, away from oxidants and other incompatible substances to prevent chemical reactions. Storage containers must be tightly sealed to prevent leakage. Labels should also be made, indicating the name of the substance, characteristics and precautions, etc., for access and management.
Fourth, related to waste disposal. Waste generated during use must not be discarded at will, and must be properly disposed of in accordance with relevant regulations and standards. Generally speaking, it should be collected in categories and handed over to professional treatment institutions for harmless disposal to avoid pollution to the environment.
Fifth, for the dosage. The dosage must be precisely controlled according to the experimental requirements or product instructions, and should not be increased or decreased at will. Excessive use will not only cause waste, but also may cause unnecessary risks; and insufficient dosage may not achieve the desired effect. In conclusion, when using 2-chloro-10,11-dihydro-11-oxo-dibenzo [b, f] [1,4] oxazepines, every step of the operation needs to be done with caution and must not be taken lightly, so as to ensure safety and effectiveness.
First, it is related to safety protection. This substance may be toxic and irritating. When contacting, you must be fully armed, wear protective clothing, gloves, and wear goggles and gas masks to prevent it from coming into contact with the skin, eyes, or inhaling into the body, endangering personal safety. After the operation, be sure to wash your hands and expose your skin to prevent adverse effects from residual substances.
Second, about the operating environment. It is necessary to operate in a well-ventilated place, preferably in a fume hood, which can effectively disperse volatile gases and reduce the concentration of harmful substances in the air. At the same time, the operation site should be away from fire and heat sources, because it may be flammable, in case of open fire, hot topic may cause combustion or even explosion, resulting in disaster.
Third, involving storage requirements. It should be stored in a cool, dry and ventilated place, away from oxidants and other incompatible substances to prevent chemical reactions. Storage containers must be tightly sealed to prevent leakage. Labels should also be made, indicating the name of the substance, characteristics and precautions, etc., for access and management.
Fourth, related to waste disposal. Waste generated during use must not be discarded at will, and must be properly disposed of in accordance with relevant regulations and standards. Generally speaking, it should be collected in categories and handed over to professional treatment institutions for harmless disposal to avoid pollution to the environment.
Fifth, for the dosage. The dosage must be precisely controlled according to the experimental requirements or product instructions, and should not be increased or decreased at will. Excessive use will not only cause waste, but also may cause unnecessary risks; and insufficient dosage may not achieve the desired effect. In conclusion, when using 2-chloro-10,11-dihydro-11-oxo-dibenzo [b, f] [1,4] oxazepines, every step of the operation needs to be done with caution and must not be taken lightly, so as to ensure safety and effectiveness.
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