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2-Chloro-10,11-Dihydro-11-Oxo-Dibenzene(B.F.)(1,4)-Oxazepine
Linshang Chemical
|
HS Code |
710010 |
| Chemical Formula | C15H10ClNO2 |
| Molar Mass | 271.7 g/mol |
| Appearance | Solid |
| Melting Point | Data needed |
| Boiling Point | Data needed |
| Solubility In Water | Low solubility |
| Solubility In Organic Solvents | Soluble in some organic solvents |
| Density | Data needed |
| Vapor Pressure | Data needed |
| Pka | Data needed |
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 packaging. |
| Storage | 2 - chloro - 10,11 - dihydro - 11 - oxo - dibenz[b,f][1,4]oxazepine should be stored in a cool, dry place. Keep it away from heat sources, open flames, and direct sunlight. Store in a well - ventilated area to prevent the buildup of vapors. It should be isolated from incompatible substances, like strong oxidizers, to avoid potential chemical reactions. Use appropriate containers, preferably tightly - sealed ones, to prevent leakage. |
| Shipping | 2 - chloro - 10,11 - dihydro - 11 - oxo - dibenz(b,f)(1,4)oxazepine is a chemical. Shipping requires proper packaging in accordance with hazardous material regulations, ensuring leak - proof containers and clear labeling for safe transportation. |
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.
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As a leading 2-Chloro-10,11-Dihydro-11-Oxo-Dibenzene(B.F.)(1,4)-Oxazepine supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
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, an organic compound. Its molecular structure is quite characteristic. It is composed of the parent nuclear structure of dibenzo (b, f) (1,4) -oxazepine, and is modified by the substitution of specific atoms and groups.
First, the parent nucleus of dibenzo (b, f) (1,4) -oxazepine is composed of two benzene rings fused with a seven-membered heterocycle containing nitrogen and oxygen. The two benzene rings are associated with the seven-membered heterocycle in a specific spatial orientation, giving the molecule a specific planarity and rigidity. This parent nucleus structure exists widely in many organic compounds, serving as the basic skeleton of molecules and laying the foundation for their physical and chemical properties.
On the parent nucleus, the 10- and 11-position carbons are double-bonded, and the 11-position oxygen atom and carbon are double-bonded to form a carbonyl structure. The presence of carbonyl groups greatly affects the chemical activity of molecules. Due to its strong polarity, the electron cloud is biased towards the oxygen atom, making the 11-position carbon positive, vulnerable to nucleophilic reagents and participating in many chemical reactions, such as nucleophilic addition reactions.
The substitution of the 2-position chlorine atom also has a significant impact on the molecular properties. Chlorine atoms are highly electronegative, and the electron-absorbing induction effect reduces the density of electron clouds in the ortho and para-position, alters the electron distribution of the molecule, and then affects the reactivity and physical properties of the molecule. For example, the introduction of chlorine atoms can enhance the lipid solubility of molecules and affect their solubility in different solvents. In the field of drug research and development, this property is related to the absorption, distribution and metabolism of drugs.
Overall, the chemical structure of 2-chloro-10,11-dihydro-11-oxo-dibenzo (b, f) (1,4) -oxazepines is determined by the interaction between the unique parent nuclear structure and specific substituents.
First, the parent nucleus of dibenzo (b, f) (1,4) -oxazepine is composed of two benzene rings fused with a seven-membered heterocycle containing nitrogen and oxygen. The two benzene rings are associated with the seven-membered heterocycle in a specific spatial orientation, giving the molecule a specific planarity and rigidity. This parent nucleus structure exists widely in many organic compounds, serving as the basic skeleton of molecules and laying the foundation for their physical and chemical properties.
On the parent nucleus, the 10- and 11-position carbons are double-bonded, and the 11-position oxygen atom and carbon are double-bonded to form a carbonyl structure. The presence of carbonyl groups greatly affects the chemical activity of molecules. Due to its strong polarity, the electron cloud is biased towards the oxygen atom, making the 11-position carbon positive, vulnerable to nucleophilic reagents and participating in many chemical reactions, such as nucleophilic addition reactions.
The substitution of the 2-position chlorine atom also has a significant impact on the molecular properties. Chlorine atoms are highly electronegative, and the electron-absorbing induction effect reduces the density of electron clouds in the ortho and para-position, alters the electron distribution of the molecule, and then affects the reactivity and physical properties of the molecule. For example, the introduction of chlorine atoms can enhance the lipid solubility of molecules and affect their solubility in different solvents. In the field of drug research and development, this property is related to the absorption, distribution and metabolism of drugs.
Overall, the chemical structure of 2-chloro-10,11-dihydro-11-oxo-dibenzo (b, f) (1,4) -oxazepines is determined by the interaction between the unique parent nuclear structure and specific substituents.
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, this medicine is a good medicine for sedation, hypnosis and anti-anxiety, and is quite useful in the medical way.
Looking at its pharmacology, it can calm the mind and make the upset state gradually calm down. In the case of insomnia, it can help the patient fall asleep and enjoy a peaceful sleep, just like a boat on a night voyage to find a peaceful harbor. In the case of anxiety, it can relieve tension, such as spring breeze and rain, moisturizing the anxious heart.
The reason for its action, or related to the regulation of the nervous system, acts on the corresponding receptors, adjusts the transmission of neurotransmitters, and achieves the effect of calming the mind. In various diseases, such as insomnia, generalized anxiety disorder, etc., you can try this medicine, but the way of taking medicine should be followed by the doctor, and you should not act without authorization, so as not to cause adverse results.
Looking at its pharmacology, it can calm the mind and make the upset state gradually calm down. In the case of insomnia, it can help the patient fall asleep and enjoy a peaceful sleep, just like a boat on a night voyage to find a peaceful harbor. In the case of anxiety, it can relieve tension, such as spring breeze and rain, moisturizing the anxious heart.
The reason for its action, or related to the regulation of the nervous system, acts on the corresponding receptors, adjusts the transmission of neurotransmitters, and achieves the effect of calming the mind. In various diseases, such as insomnia, generalized anxiety disorder, etc., you can try this medicine, but the way of taking medicine should be followed by the doctor, and you should not act without authorization, so as not to cause adverse results.
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, this is an organic compound. Its physical properties are related to many aspects, let me explain them one by one.
Looking at its appearance, under normal temperature and pressure, it is mostly in the state of white to light yellow crystalline powder, just like fine snowflakes or soft golden sand, delicate and warm in color. This form is easy to store and use, and is also conducive to dispersion and participation in many chemical reactions.
The melting point is between 180 and 184 ° C. The melting point is the critical temperature at which a substance melts from a solid state to a liquid state. When the temperature rises to this range, the compound slowly turns from solid to liquid, just like ice and snow melting in the warm sun. This property is crucial for the purification, identification and control of the synthesis process of the compound. Knowing the melting point, the purity can be judged by the melting point measurement. If the purity is high, the melting point range is narrow and close to the theoretical value; if it contains impurities, the melting point decreases and the range becomes wider.
In terms of solubility, it is soluble in common organic solvents such as dichloromethane, chloroform, and N, N-dimethylformamide (DMF), just like fish get water, and can be evenly dispersed. However, the solubility in water is very small, just like the incompatibility of oil and water. This solubility characteristic allows it to choose a suitable organic solvent according to the reaction requirements during the organic synthesis reaction to ensure the smooth progress of the reaction. At the same time, in the separation and purification step, it can be separated from other substances by virtue of its solubility difference.
In addition, the density of the compound is also an important physical property. Although the exact value varies depending on the measurement conditions, the approximate range allows us to understand its space and mass distribution in a specific environment. The difference in density has a profound impact on the separation of mixtures and preparation of preparations.
Furthermore, its stability cannot be ignored. Under normal storage conditions, it can maintain a relatively stable state in a dry and cool place. However, if exposed to high temperature, high humidity or strong light, it may decompose or deteriorate, just like a delicate flower cannot withstand the hot sun and rainstorm. Therefore, when storing and transporting, it is necessary to strictly control the environmental conditions to maintain the stability of its chemical structure and properties.
Looking at its appearance, under normal temperature and pressure, it is mostly in the state of white to light yellow crystalline powder, just like fine snowflakes or soft golden sand, delicate and warm in color. This form is easy to store and use, and is also conducive to dispersion and participation in many chemical reactions.
The melting point is between 180 and 184 ° C. The melting point is the critical temperature at which a substance melts from a solid state to a liquid state. When the temperature rises to this range, the compound slowly turns from solid to liquid, just like ice and snow melting in the warm sun. This property is crucial for the purification, identification and control of the synthesis process of the compound. Knowing the melting point, the purity can be judged by the melting point measurement. If the purity is high, the melting point range is narrow and close to the theoretical value; if it contains impurities, the melting point decreases and the range becomes wider.
In terms of solubility, it is soluble in common organic solvents such as dichloromethane, chloroform, and N, N-dimethylformamide (DMF), just like fish get water, and can be evenly dispersed. However, the solubility in water is very small, just like the incompatibility of oil and water. This solubility characteristic allows it to choose a suitable organic solvent according to the reaction requirements during the organic synthesis reaction to ensure the smooth progress of the reaction. At the same time, in the separation and purification step, it can be separated from other substances by virtue of its solubility difference.
In addition, the density of the compound is also an important physical property. Although the exact value varies depending on the measurement conditions, the approximate range allows us to understand its space and mass distribution in a specific environment. The difference in density has a profound impact on the separation of mixtures and preparation of preparations.
Furthermore, its stability cannot be ignored. Under normal storage conditions, it can maintain a relatively stable state in a dry and cool place. However, if exposed to high temperature, high humidity or strong light, it may decompose or deteriorate, just like a delicate flower cannot withstand the hot sun and rainstorm. Therefore, when storing and transporting, it is necessary to strictly control the environmental conditions to maintain the stability of its chemical structure and properties.
What are the synthesis methods of 2-chloro-10,11-dihydro-11-oxo-dibenzene (b.f.) (1,4) -oxazepine?
The synthesis of 2-chloro-10,11-dihydro-11-oxo-dibenzo (b, f) (1,4) oxazepines is an important research direction in the field of chemistry. In the past, the synthesis of this compound often relied on a multi-step reaction.
Initially, with suitable starting materials, such as benzene derivatives with specific substituents, chlorine atoms are introduced at key positions through halogenation. This step requires fine control of reaction conditions, such as temperature, reactant ratio, and catalyst selection, to ensure precise substitution of chlorine atoms.
Then, with the help of cyclization, the basic skeleton of dibenzo (b, f) (1,4) oxazepines is constructed. This process may involve nucleophilic substitution or electrophilic reactions in molecules, etc. Appropriate reaction media and accelerators are required to promote the rearrangement and closure of the molecular structure to form the desired cyclic structure.
Repeated, the obtained intermediate product is modified by oxidation or reduction to achieve the target structure of 11-oxo generation. During this period, mild and efficient oxidizing or reducing agents are selected to avoid unnecessary effects on other functional groups.
Recently, new catalytic systems or green chemical methods are also used. If transition metal catalysis is used, the selectivity and efficiency of the reaction can be improved, and the occurrence of side reactions can be reduced. The green chemistry path focuses on the use of environmentally friendly solvents and the reduction of waste generation, which is in line with the current concept of sustainable development. However, on the road of synthesis, chemists still need to study the reaction mechanism of each step in detail and fine-tune the conditions to obtain 2-chloro-10,11-dihydro-11-oxo-dibenzo (b, f) (1,4) oxazepines with high yield and high purity.
Initially, with suitable starting materials, such as benzene derivatives with specific substituents, chlorine atoms are introduced at key positions through halogenation. This step requires fine control of reaction conditions, such as temperature, reactant ratio, and catalyst selection, to ensure precise substitution of chlorine atoms.
Then, with the help of cyclization, the basic skeleton of dibenzo (b, f) (1,4) oxazepines is constructed. This process may involve nucleophilic substitution or electrophilic reactions in molecules, etc. Appropriate reaction media and accelerators are required to promote the rearrangement and closure of the molecular structure to form the desired cyclic structure.
Repeated, the obtained intermediate product is modified by oxidation or reduction to achieve the target structure of 11-oxo generation. During this period, mild and efficient oxidizing or reducing agents are selected to avoid unnecessary effects on other functional groups.
Recently, new catalytic systems or green chemical methods are also used. If transition metal catalysis is used, the selectivity and efficiency of the reaction can be improved, and the occurrence of side reactions can be reduced. The green chemistry path focuses on the use of environmentally friendly solvents and the reduction of waste generation, which is in line with the current concept of sustainable development. However, on the road of synthesis, chemists still need to study the reaction mechanism of each step in detail and fine-tune the conditions to obtain 2-chloro-10,11-dihydro-11-oxo-dibenzo (b, f) (1,4) oxazepines with high yield and high purity.
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 using this compound, there are a number of urgent precautions to be taken.
First, it is related to safety protection. This compound may be toxic and irritating to some extent. When operating, be sure to wear appropriate protective equipment, such as laboratory clothes, gloves and goggles, to avoid direct contact with the skin and eyes. And the operation should be carried out in a well-ventilated place or in a fume hood to prevent inhalation of its volatile aerosols and damage to the respiratory system.
Second, about storage conditions. It should be stored in a cool, dry and ventilated place, away from fire and heat sources. It should be stored separately from oxidizing agents, acids, alkalis and other substances to avoid dangerous chemical reactions caused by mixed storage.
Third, in the process of taking and weighing. The operation must be fine, and clean and precise utensils should be used. After taking it, seal the container in time to prevent it from being damp, oxidized or contaminated by other impurities, which will affect its quality and performance.
Fourth, during the experimental operation. Strictly follow the established experimental procedures and operating methods. If chemical reactions are involved, the reaction conditions such as temperature, pressure, reaction time and other parameters must be precisely controlled, so as not to cause the reaction to run out of control due to deviations in conditions, generate unexpected products, or even cause safety accidents.
Fifth, after use. Dispose of the residue should not be neglected. Dispose of it properly in accordance with relevant environmental regulations and laboratory regulations, and must not be discarded at will to prevent pollution to the environment.
First, it is related to safety protection. This compound may be toxic and irritating to some extent. When operating, be sure to wear appropriate protective equipment, such as laboratory clothes, gloves and goggles, to avoid direct contact with the skin and eyes. And the operation should be carried out in a well-ventilated place or in a fume hood to prevent inhalation of its volatile aerosols and damage to the respiratory system.
Second, about storage conditions. It should be stored in a cool, dry and ventilated place, away from fire and heat sources. It should be stored separately from oxidizing agents, acids, alkalis and other substances to avoid dangerous chemical reactions caused by mixed storage.
Third, in the process of taking and weighing. The operation must be fine, and clean and precise utensils should be used. After taking it, seal the container in time to prevent it from being damp, oxidized or contaminated by other impurities, which will affect its quality and performance.
Fourth, during the experimental operation. Strictly follow the established experimental procedures and operating methods. If chemical reactions are involved, the reaction conditions such as temperature, pressure, reaction time and other parameters must be precisely controlled, so as not to cause the reaction to run out of control due to deviations in conditions, generate unexpected products, or even cause safety accidents.
Fifth, after use. Dispose of the residue should not be neglected. Dispose of it properly in accordance with relevant environmental regulations and laboratory regulations, and must not be discarded at will to prevent pollution to the environment.
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