1h Pyrrolo 2 3 C Pyridine 2 Carboxylic Acid 5 Chloro
pyridine pyrrole pyrazine piperidine piperazine

1H-Pyrrolo[2,3-c]pyridine-2-carboxylic acid, 5-chloro-

    Specifications

    HS Code

    778284

    Name 5-chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxylic acid
    Molecular Formula C8H5ClN2O2
    Molecular Weight 196.59
    Appearance Solid (predicted)
    Boiling Point 474.3°C at 760 mmHg (predicted)
    Melting Point 257 - 259°C
    Density 1.602 g/cm³ (predicted)
    Pka 1.77±0.20 (predicted)
    Solubility Soluble in DMSO, DMF, slightly soluble in methanol
    Logp 1.49 (predicted)
    Refractive Index 1.732 (predicted)

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    General Information
    Where to Buy 1H-Pyrrolo[2,3-c]pyridine-2-carboxylic acid, 5-chloro- in China?
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    Frequently Asked Questions

    As a leading 1H-Pyrrolo[2,3-c]pyridine-2-carboxylic acid, 5-chloro- supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What are the chemical properties of 1H-Pyrrolo [2,3-c] pyridine-2-carboxylic acid, 5-chloro-
    5-Chloro-1H-pyrrolido [2,3-c] pyridine-2-carboxylic acid, this is an organic compound. It is acidic and can release protons in a suitable medium due to its carboxyl group.
    From a structural perspective, the pyridine ring fuses with the pyrrole ring, giving the compound a special conjugate system, which affects its electron cloud distribution and stability. The introduction of chlorine atoms alters the electron density and steric resistance of the molecule.
    In terms of physical properties, its solubility may vary depending on the polarity of the molecule. The presence of carboxyl groups increases its solubility in polar solvents. Its melting point and boiling point are also determined by intermolecular forces, such as hydrogen bonds, van der Waals forces, etc.
    In terms of chemical properties, carboxyl groups can participate in many reactions, such as esters, which react with alcohols under the action of catalysts to form corresponding esters; they can also react with bases to form salts. Hydrogen atoms on pyridine rings and pyrrole rings have certain reactivity due to the influence of conjugation systems, and can participate in electrophilic substitution reactions, while chlorine atoms can be replaced by nucleophiles, resulting in a variety of chemical transformations, which have great application potential in the field of organic synthesis.
    What is the main use of 1H-Pyrrolo [2,3-c] pyridine-2-carboxylic acid, 5-chloro-
    5-Chloro-1H-pyrrolido [2,3-c] pyridine-2-carboxylic acid has a wide range of uses. In the field of medicine, it is often used as a key intermediate for the synthesis of a variety of drugs with special curative effects. Due to the unique chemical structure of this compound, it has the ability to interact with specific targets in organisms. Through carefully designed chemical reactions, it can be converted into drugs for the treatment of diseases such as cardiovascular diseases, neurological diseases and tumors.
    It also has important applications in the field of pesticides. Because of its certain biological activity, it can be modified and modified to develop highly efficient and low-toxic pesticide products. Such pesticides can precisely act on the specific physiological processes of pests or pathogens, inhibit their growth and reproduction, and achieve the purpose of crop protection, and have relatively little impact on the environment, which is in line with the current needs of green agriculture development.
    In the field of materials science, 5-chloro-1H-pyrrolido [2,3-c] pyridine-2-carboxylic acid can also play an important role. It can be used as a basic raw material for the construction of new functional materials. By polymerization or coordination with other compounds, materials with special optical, electrical or magnetic properties can be prepared, which are expected to be applied to many cutting-edge scientific and technological fields such as optoelectronic devices and sensors, and promote the development and innovation of related industries.
    What are the synthesis methods of 1H-Pyrrolo [2,3-c] pyridine-2-carboxylic acid, 5-chloro-
    The synthesis method of 5-chloro-1H-pyrrolido [2,3-c] pyridine-2-carboxylic acid is a key investigation in the field of organic synthesis. To make this substance, common methods include specific pyridine derivatives as starting materials.
    First, a pyridine compound containing an appropriate substituent can be taken first, and the chlorine atom is introduced into the designated position through halogenation reaction. In this halogenation process, a suitable halogenation reagent, such as a chlorine-containing halogenating agent, should be selected, and the reaction conditions, such as temperature and solvent, should be controlled to ensure that the chlorine atom falls precisely at the expected check point. Then, through ingenious cyclization reaction, the core structure of pyrrolido-pyridine is constructed. This cyclization step may require the help of a catalyst to promote the formation of intra-molecular rings and form the basic structure of the target product.
    Furthermore, other heterocyclic compounds are also used as the starting point and obtained through multi-step transformation. First, the functional group of the initial heterocyclic ring is modified, and an active group that can be further reacted is introduced. Then, through a series of reactions such as condensation and closed-loop, the structure of the target molecule is gradually built. In this process, each step of the reaction needs to be carefully controlled. From the ratio of reactants to the determination of reaction time and temperature, it is all about success or failure.
    Or the reaction strategy of transition metal catalysis can be used. Transition metal catalysts, such as palladium, copper and other metal complexes, are used to catalyze the coupling reaction between specific substrates to realize the construction of carbon-carbon or carbon-heteroatomic bonds. In this way, molecular fragments are gradually spliced to achieve the synthesis of 5-chloro-1H-pyrrolido [2,3-c] pyridine-2-carboxylic acid. And in the synthesis process, it is necessary to use separation and purification techniques, such as column chromatography, recrystallization, etc. in a timely manner to obtain high-purity products. Such various methods are all effective ways to synthesize this compound, but the advantages and disadvantages of each method are mutually exclusive, and it is necessary to carefully choose according to actual needs and conditions.
    1H-Pyrrolo [2,3-c] pyridine-2-carboxylic acid, 5-chloro - what is the price range in the market
    In today's world, it is difficult to determine the market price of 1H - Pyrrolo [2,3 - c] pyridine - 2 - carboxylic acid, 5 - chloro -. The price of this compound, or involved in pharmaceutical research and development, chemical research and many other fields, is determined by multiple factors.
    As far as the raw materials are concerned, if the raw materials required to synthesize this compound are rare or difficult to prepare, the price must be high. If the raw materials need to be refined through complicated processes, or are obtained from rare materials, the cost will increase greatly, which will then push up the price of the product.
    When it comes to the synthesis process, if the synthesis requires high-precision technology, or requires severe reaction conditions, such as specific temperature and pressure, and the requirements for the reaction equipment are very high, or the synthesis steps are cumbersome and lengthy, requiring multiple purification and refining, all of which will cause the production cost to soar and the price to rise.
    Market supply and demand is also the key. If many pharmaceutical companies and scientific research institutions have strong demand for it, but the supply is limited and the supply is in short supply, the price will rise; conversely, if the demand is low and the supply is sufficient, the price will fall.
    In addition, the scale of production also has an impact. In large-scale production, due to the scale effect, the unit cost may be reduced, and the price may be more affordable; if only small-scale production, the cost is difficult to decrease, and the price will be relatively high.
    Overall, the price of this compound in the market may fluctuate within a large range. For ordinary scientific research dosage, if the raw materials are easy to obtain and the process is conventional, the price per gram may be in the hundreds of yuan; if the raw materials are rare and the process is complicated, the price per gram may exceed 1,000 yuan, or even higher. However, this is only a guess. The actual price needs to be determined by carefully observing the dynamics of the market and the quotations of various suppliers.
    What are the storage conditions for 1H-Pyrrolo [2,3-c] pyridine-2-carboxylic acid, 5-chloro-
    5-Chloro-1H-pyrrolido [2,3-c] pyridine-2-carboxylic acid, its storage is important, related to physical properties, need to be cautious. This substance has specific chemical properties and is susceptible to the surrounding environment.
    Its storage environment is the first to dry. If it is in a humid place, water vapor is easy to interact with it, or cause deterioration, affecting its chemical structure and purity. Therefore, when choosing a dry place, if conditions permit, a desiccant can be placed next to it to absorb moisture and keep it pure.
    Temperature is also key. It should be stored in a cool place to avoid high temperature and hot topics. Due to high temperature, it can promote its chemical reaction, causing decomposition, polymerization and other adverse changes. The ideal temperature is between 2 and 8 degrees Celsius, which can stabilize its chemical properties and prolong its storage.
    Furthermore, it should not be ignored when protected from light. Optical radiation or photochemical reactions cause damage to its quality. Therefore, it should be stored in an opaque container or stored in a dark place to prevent light from contacting objects.
    In addition, the storage place should be well ventilated. If it is closed and the air does not flow, the volatile gas will accumulate and not disperse, or cause danger, or affect the substance itself. < Br >
    And because it may be toxic and corrosive, it must be separated from other objects when storing, especially with active metals, strong oxidizing agents, etc., to prevent accidental reactions and ensure storage safety. When handling and storing, you should also follow safety procedures and wear protective equipment to protect personal safety. In this way, it can be properly stored and its properties are stable for later use.