2 Chloro 4 Methyl 6 7 Dihydro 5h Cyclopenta B Pyridine
pyridine pyrrole pyrazine piperidine piperazine

2-chloro-4-methyl-6,7-dihydro-5H-cyclopenta[b]pyridine

    Specifications

    HS Code

    542925

    Chemical Formula C9H10ClN
    Physical State Solid (predicted)
    Boiling Point 273.3°C at 760 mmHg (predicted)
    Melting Point N/A
    Density 1.177 g/cm³ (predicted)
    Flash Point 119.1°C (predicted)
    Water Solubility Insoluble (predicted)
    Logp 2.64 (predicted)
    Vapor Pressure 0.00262 mmHg at 25°C (predicted)

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    What are the physical properties of 2-chloro-4-methyl-6, 7-dihydro-5H-cyclopenta [b] pyridine
    2-Chloro-4-methyl-6,7-dihydro-5H-cyclopento [b] pyridine, this is an organic compound. Its physical properties are unique, let me explain in detail.
    Looking at its appearance, it is often a colorless to light yellow liquid or solid, which varies depending on the temperature and pressure of the surrounding environment. Under normal temperature and pressure, or a flowing liquid, if the temperature decreases, it may condense into a solid state.
    When it comes to melting point, there is no exact constant, because the compound has a special structure, complex intermolecular forces, and is greatly affected by impurities and crystal forms. However, the approximate range may be determined experimentally. This process requires strict control of conditions in order to obtain more accurate data.
    The boiling point is also a key physical property. Generally speaking, due to the chlorine atom, methyl group and special cyclopentopyridine structure in the molecule, the intermolecular force is enhanced, resulting in a relatively high boiling point. However, the specific value needs to be determined by professional distillation experiments, under conditions such as precise control of pressure.
    In terms of solubility, it has a certain solubility in organic solvents such as ethanol, ether, dichloromethane, etc. This is because the structure of the compound has both a certain polar and non-polar region, and it can interact with organic solvents through intermolecular forces. In water, the solubility is relatively small, because its non-polar part is larger, and the polarity difference with water is significant, following the principle of "similarity and compatibility".
    Density is also a consideration. Its density is slightly greater or smaller than that of water when compared with water, or due to the composition and structure of molecules. To accurately determine the density, it is necessary to use professional density measuring instruments, such as symmetry bottles, to obtain reliable data after multiple measurements and averages. < Br >
    The physical properties of 2-chloro-4-methyl-6,7-dihydro-5H-cyclopento [b] pyridine are profoundly influenced by structure and vary under different conditions. These properties need to be carefully considered during research and application.
    What are the chemical properties of 2-chloro-4-methyl-6, 7-dihydro-5H-cyclopenta [b] pyridine
    2-Chloro-4-methyl-6,7-dihydro-5H-cyclopento [b] pyridine, this is an organic compound. Its chemical properties are unique and there are many things worth exploring.
    First of all, its physical properties are usually solid at room temperature. Its structure contains cyclic and heterocyclic parts, and intermolecular forces or cause it to be in a solid state. The melting boiling point is affected by intermolecular interactions. The presence of heterocyclic and chlorine atoms and methyl groups may enhance the intermolecular forces, causing the melting boiling point to rise. And the relative molecular mass of the compound or larger, also has an impact on the melting boiling point.
    Let's talk about chemical properties. Its chemical activity comes from key groups in the structure. Chlorine atoms have strong electronegativity, which is a check point for the activity of nucleophilic substitution reactions. Nucleophilic reagents can attack the carbon atoms attached to chlorine, and the chlorine atoms leave to form new organic compounds. For example, when reacting with sodium alcohol, anion alcohol oxide acts as a nucleophilic reagent to replace chlorine atoms and form ether compounds. The double bond in the
    molecule is also an important active site. Addition reactions can occur, such as reacting with bromine water, the double bond is opened, and the bromine atom is added to the double bond carbon atom to form a dibromogen. This reaction exhibits its unsaturated bond characteristics, similar to the mechanism of the double bond addition reaction of olefins.
    In addition, the pyridine cyclic nitrogen atom has a pair of lone pairs of electrons and has a certain alkalinity. Under acidic conditions, the nitrogen atom can accept protons and form a pyridine salt. This property affects its existence form and reactivity in different acid-base environments.
    At the same time, due to the existence of a cyclopentopyridine structure conjugated system, the compound has certain stability. The conjugated system delocalizes electrons and reduces molecular energy. But under specific conditions, such as the action of a strong oxidant, the conjugated system may be destroyed and an oxidation reaction occurs.
    In summary, 2-chloro-4-methyl-6,7-dihydro-5H-cyclopento [b] pyridine has a unique structure, nucleophilic substitution, addition, acidity and alkalinity, and the stability and oxidizability of conjugate-based systems. These properties are of great significance in the fields of organic synthesis and medicinal chemistry.
    What is the main synthesis method of 2-chloro-4-methyl-6, 7-dihydro-5H-cyclopenta [b] pyridine
    The main synthesis method of 2-chloro-4-methyl-6,7-dihydro-5H-cyclopento [b] pyridine has attracted much attention in the field of chemistry. There are several common methods for synthesizing this compound.
    One is through cyclization. With appropriate starting materials and carefully designed reaction steps, intracellular cyclization is promoted, and then the core structure of cyclopento [b] pyridine is constructed. This process requires precise regulation of reaction conditions, such as temperature, reaction time, and reactant ratio. Too high or too low temperature may cause the reaction to be biased towards side reactions, and improper reactant ratio will also affect the yield and purity of the product.
    The second is the method of catalysis with the help of transition metals. Transition metal catalysts can play a key role in such reactions, which can effectively promote the formation of carbon-carbon bonds or carbon-heteroatomic bonds. In this process, it is necessary to carefully select suitable transition metal catalysts and their ligands. Due to different combinations of catalysts and ligands, the selectivity and activity of the reaction are greatly affected. At the same time, the choice of reaction solvent is also very important. The polarity and solubility of different solvents will affect the reaction rate and product distribution.
    The third is to use a multi-step reaction strategy. The key intermediate is prepared first, and then the multi-step functional group conversion is carried out to finally achieve the synthesis of the target product. This strategy requires strict monitoring and optimization of each reaction step to ensure the yield and product purity of each step. After each reaction step, separation and purification operations are often required to remove impurities and provide pure raw materials for the next reaction.
    Synthesis of 2-chloro-4-methyl-6,7-dihydro-5H-cyclopento [b] pyridine requires comprehensive consideration of reaction conditions, raw material selection, catalyst and many other factors. By optimizing each reaction step, the ideal synthesis effect can be obtained.
    Where is 2-chloro-4-methyl-6, 7-dihydro-5H-cyclopenta [b] pyridine used?
    2-Chloro-4-methyl-6,7-dihydro-5H-cyclopento [b] pyridine, this compound has applications in medicine, pesticides, materials science and other fields.
    In the field of medicine, due to its unique chemical structure, it can be used as a key intermediate to synthesize many drugs. This structure gives it the possibility to interact with specific targets in organisms, such as specific receptors or enzymes related to certain diseases. Scientists can modify the structure of this compound to optimize its affinity and selectivity with targets to develop drugs for the treatment of cardiovascular diseases, neurological diseases, cancers and other drugs. For example, the structural modification of its chlorine atom, methyl and cyclopentopyridine ring parts may lead to new compounds with better pharmacological activities and pharmacokinetic properties.
    In the field of pesticides, 2-chloro-4-methyl-6,7-dihydro-5H-cyclopentopyridine can be used as an important cornerstone for the construction of high-efficiency pesticides. Its structural properties or make it have certain biological activities, which can play a role in specific physiological processes of pests, such as interfering with the transmission of the pest's nervous system, inhibiting its growth and development, or affecting its reproductive ability. After rational structural optimization and formulation design, new pesticides with high toxic activity against specific pests, environmental friendliness and non-target biosafety may be developed.
    In the field of materials science, this compound can be used to prepare functional materials with unique properties due to its special structure. For example, introducing it into the structure of polymer materials may endow materials with special optical, electrical or thermal properties. It may participate in polymerization reactions to form polymers with specific functional groups, which can be used to prepare optoelectronic materials, sensor materials, etc., providing new directions and options for the development of materials science.
    What is the market outlook for 2-chloro-4-methyl-6, 7-dihydro-5H-cyclopenta [b] pyridine
    Today, there are 2-chloro-4-methyl-6,7-dihydro-5H-cyclopento [b] pyridine, and its market prospect is quite promising. Looking at today's chemical industry, there is a growing demand for many fine chemicals, and this compound has great potential in the process of drug synthesis.
    Because of its unique structure, it can be used as a key intermediate, which can pave a way for developers in the creation of new drugs. For example, in the development of therapeutic drugs for certain specific diseases, its structural properties may be in line with disease-related targets, thereby facilitating the development of new drugs and solving the suffering of patients.
    Furthermore, in the field of materials science, with the advancement of science and technology, the search for materials with special properties is endless. 2-Chloro-4-methyl-6,7-dihydro-5H-cyclopento [b] pyridine may be introduced into the polymer material system through specific reactions, endowing the material with unique optical and electrical properties, and expanding the boundaries of material application.
    However, its market prospects are not smooth. The simplicity of the preparation process is related to the production cost. If the process can be optimized, the cost can be reduced and the efficiency can be increased, and it can take the lead in the market competition. And changes in regulations and policies, and the rise in environmental protection requirements are all considerations for its development. Under the premise of compliance, seek development strategies. In short, although challenges coexist, opportunities are abundant. With time, good management will be able to gain a place in the market.