1h Pyrazolo 4 3 C Pyridine 4 6 Dichloro
pyridine pyrrole pyrazine piperidine piperazine

1H-Pyrazolo[4,3-c]pyridine, 4,6-dichloro-

    Specifications

    HS Code

    818867

    Chemical Formula C7H3Cl2N3
    Molecular Weight 199.98
    Appearance Solid (predicted)
    Boiling Point Estimated around 362.4°C at 760 mmHg
    Density Estimated around 1.64 g/cm³
    Solubility Poorly soluble in water, soluble in organic solvents like dichloromethane
    Pka No common pKa data found (likely weakly basic due to nitrogen in heterocyclic rings)
    Logp Estimated around 3.1 (lipophilic)
    Vapor Pressure Very low vapor pressure, solid at room conditions

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    General Information
    Where to Buy 1H-Pyrazolo[4,3-c]pyridine, 4,6-dichloro- in China?
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    Frequently Asked Questions

    As a leading 1H-Pyrazolo[4,3-c]pyridine, 4,6-dichloro- 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 main use of 1H-pyrazolo [4,3-c] pyridine, 4,6-dichloro-
    1H-pyrazolo [4,3-c] pyrazole, 4,6-dihydro-has a wide range of uses. In the field of medicine, it is often used as an active ingredient because of its unique chemical structure and biological activity, which can interact with specific biological targets. For example, when developing new antimalarial drugs, this structure can effectively interfere with the metabolic process of malaria parasites, so as to achieve the purpose of treating malaria; in the development of anti-tumor drugs, it may inhibit the proliferation of tumor cells and induce their apoptosis.
    In the field of pesticides, 1H-pyrazolo [4,3-c] pyrazole, 4,6-dihydro-compounds are also of important value. It can be made into insecticides, which can kill a variety of pests by interfering with the nervous system or physiological metabolic pathways of insects, and is relatively friendly to the environment, with less residue, and can reduce the damage to ecological balance. In terms of fungicides, it can resist a variety of plant pathogens, ensure the healthy growth of crops, and improve crop yield and quality.
    In the field of materials science, due to its unique electronic structure and stability, it can be used to prepare functional materials. For example, in organic photoelectric materials, it can improve the photoelectric properties of materials, and be applied to devices such as Light Emitting Diodes and solar cells to improve their efficiency and stability, providing assistance for the development of new energy and display technologies.
    What are the synthesis methods of 1H-pyrazolo [4,3-c] pyridine, 4,6-dichloro-
    The synthesis method of 1H-pyrazolo [4,3-c] pyrazole, 4,6-dihydro-involves many chemical doorways, and let me go through them one by one.
    First, it can be prepared from nitrogen-containing heterocyclic compounds through specific cyclization reactions. For example, select a suitable bifunctional precursor, which contains nitrogen at one end and is nucleophilic, and the other end is electrophilic. Under the action of suitable reaction medium and catalyst, the two interact to form an intra-molecular ring. This process requires fine regulation of reaction conditions, such as temperature, pH, etc. If the temperature is too high, or side reactions occur frequently, the product is impure; if the temperature is too low, the reaction rate is slow and takes a long time. The pH is also critical. The peracid or peralkali environment may affect the active center of the reaction, making it difficult for the reaction to proceed smoothly.
    Second, the coupling reaction catalyzed by metals is also an important path. Transition metals are used as catalysts, such as palladium and copper, which promote the coupling of nitrogen-containing substrates with other organic fragments due to their unique electronic structure and catalytic activity. This method requires consideration of the amount of metal catalysts and the choice of ligands. After different ligands are combined with metals, the activity and selectivity of the catalyst will be significantly changed. Choosing suitable ligands can effectively improve the yield and purity of the target product. At the same time, the properties of the reaction solvents should not be underestimated. Polar solvents or non-polar solvents have an impact on the reaction process and results.
    Third, it is synthesized by rearrangement reaction. Some precursors with specific structures are stimulated by external conditions, and the atoms or groups in the molecule are rearranged to construct the skeleton structure of 1H-pyrazolo [4,3-c] pyrazole and 4,6-dihydro. This process requires strict structural requirements for precursors, and precise design and synthesis are required. Moreover, the conditions for rearrangement reactions are special, which may involve high temperature, light or specific chemical agent induction. Only by controlling these conditions can efficient synthesis be achieved.
    All these synthesis methods require chemists to repeatedly explore and optimize in practice in order to achieve the ideal synthesis effect.
    What are the physical properties of 1H-pyrazolo [4,3-c] pyridine, 4,6-dichloro-
    1H-pyrazolo [4,3-c] pyrazole, 4,6-dihydro-substance, its physical properties are quite investigated. The appearance of this compound may be in a specific form, and it is usually crystalline, with white or nearly colorless color. When the quality is pure, the crystal form is regular. Under light, the luster reflected by its crystal structure can be seen, which is delicate and unique.
    When it comes to melting point, this is the key physical property. After many experiments, its melting point is in a specific temperature range. This temperature limit is relatively clear, which is determined by factors such as intermolecular forces and structural compactness. During the heating process, when this melting point is reached, the compound gradually melts from a solid state to a liquid state. This transition process is orderly and smooth, which can be an important indicator for the identification of this compound.
    Furthermore, the solubility is also the focus of consideration. In common organic solvents, their solubility varies. In polar organic solvents, such as ethanol and acetone, there may be a certain solubility, but in non-polar solvents, such as n-hexane, benzene, etc., the solubility is quite limited. This property is closely related to the polarity of the compound molecule and the hydrophobicity of the structure. It is in solution or has specific interactions with solvent molecules, such as hydrogen bonds, van der Waals forces, etc., which in turn affect its solubility.
    In addition, density is also one of its physical properties. After accurate measurement, its density value can be obtained. This value reflects the mass of the substance in a unit volume and is closely related to the molecular accumulation method and relative molecular weight of the compound. Through the determination of density, not only can the understanding of its physical nature be deepened, but also it is of important guiding significance in practical applications, such as separation and purification.
    As for its refractive index, it is also a unique physical property. When light passes through this compound, a specific degree of refraction will occur due to the influence of the internal structure of the substance on the propagation of light. Accurate determination of its refractive index can further characterize the purity and structural characteristics of the compound, which is indispensable in the field of analysis and identification. These physical properties, interrelated, together outline the unique physical features of 1H-pyrazolo [4,3-c] pyrazolo, 4,6-dihydro-compounds, laying the foundation for their applications in chemistry, materials science and other fields.
    What are the chemical properties of 1H-pyrazolo [4,3-c] pyridine, 4,6-dichloro-
    1H-pyrazolo [4,3-c] pyrazole, 4,6-dihydro-compound, its chemical properties are unique. This compound has a certain stability and can maintain its own structure at room temperature. In organic reactions, due to its special ring structure, it exhibits active reactivity.
    Looking at the nitrogen atom in its ring, it has a lone pair of electrons, which makes the compound potentially basic and can react with acids to form corresponding salts. And the conjugation system of the pyrazole ring endows it with certain aromaticity, which affects its electron cloud distribution and reaction check point selectivity.
    In the electrophilic substitution reaction, due to the difference in the density distribution of electron clouds on the ring, specific locations are more susceptible to the attack of electrophilic reagents. For example, some check point electron clouds have high density, and electrophilic reagents tend to combine with them and replace them, thereby introducing new functional groups and expanding the application range of the compound.
    In the redox reaction, the compound can act as an oxidizing agent or a reducing agent according to the reaction conditions. Under appropriate oxidation conditions, some groups on the ring can be oxidized to derive a variety of oxidation products; in the case of strong reducing agents, it can also accept electrons and undergo reduction reactions to achieve structural transformation.
    At the same time, its solubility and physical properties are also critical. In common organic solvents such as ethanol and dichloromethane, it has a certain solubility, which makes it convenient to carry out various chemical reactions and separation operations in solution systems, laying the foundation for its application in organic synthesis and medicinal chemistry.
    What is the price range of 1H-pyrazolo [4,3-c] pyridine, 4,6-dichloro-on the market?
    1H-pyrazole [4,3-c] pyrazole, 4,6-dihydro, in the market price range, it is difficult to break. Covering this compound, its price is affected by many factors.
    First, purity is the key factor. If the purity is extremely high, almost flawless, suitable for high-end scientific research experiments, it needs to be purified by a delicate and complicated method, and its price is high, or it can reach hundreds of gold per gram, or even higher. However, if the purity is slightly lower, it is only used for general basic research or specific industrial purposes, and the price should drop sharply.
    Second, the supply and demand situation also has a huge impact. If many scientific research institutions or enterprises are thirsty for it, but the supply is limited, the so-called "rare is expensive", its price will rise. On the contrary, if there is an oversupply, merchants may reduce the price in order to sell their goods.
    Third, the difficulty of preparation is also related to the price. If the synthesis steps of this compound are complicated, the required raw materials are rare and expensive, or the reaction conditions are harsh, and the equipment and technology requirements are very strict, the cost will increase greatly, and the price will also rise.
    Fourth, the market competition situation should not be ignored. If many merchants in the market sell this product, the competition is fierce, and the competition is for share, or the price will be used as a weapon to push the price down.
    Overall, under normal circumstances, the price of such compounds may fluctuate between tens of gold and hundreds of gold per gram, but this is only a rough guess. The actual price depends on specific market conditions and product quality.