7r 4 Chloro 7 1 1 Dimethylethyl Dimethylsilyl Oxy 6 7 Dihydro 5h Cyclopenta B Pyridine 3 Carbonitrile
pyridine pyrrole pyrazine piperidine piperazine

(7R)-4-Chloro-7-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-6,7-dihydro-5H-cyclopenta[b]pyridine-3-carbonitrile

    Specifications

    HS Code

    604600

    Chemical Name (7R)-4-Chloro-7-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-6,7-dihydro-5H-cyclopenta[b]pyridine-3-carbonitrile
    Molecular Formula C17H25ClN2OSi
    Molecular Weight 336.93

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    Frequently Asked Questions

    As a leading (7R)-4-Chloro-7-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-6,7-dihydro-5H-cyclopenta[b]pyridine-3-carbonitrile 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 (7R) -4-Chloro-7- [[ (1,1-dimethylethyl) dimethylsilyl] oxy] -6, 7-dihydro-5H-cyclopenta [b] pyridine-3-carbonitrile
    (7R) - 4 -chloro-7- [ (1,1 -dimethylethyl) dimethylsilyl] oxy-6,7 -dihydro-5H -cyclopento [b] pyridine-3 -formonitrile, the chemical structure of this compound is expressed in the ancient French dialect of Tiangong Kaiwu as follows:
    Look at this (7R) - 4 -chloro-7- [ (1,1 -dimethylethyl) dimethylsilyl] oxy-6,7 -dihydro-5H -cyclopento [b] pyridine-3 -methyl Nitrile, the core structure of which is the parent nucleus of cyclopento [b] pyridine. The pyridine ring is a hexagonal nitrogen-containing heterocycle with aromatic properties. At the 3rd position of the pyridine ring, there is a formonitrile group, and this -CN group is a nitrile group, which has a certain chemical activity.
    At the 4th position of the pyridine ring, there is a chlorine atom connected, and the electronegativity of the chlorine atom is relatively large, which has a significant impact on the electron cloud distribution and chemical properties of the molecule. At the 7th position, there is a long chain substituent, namely [ (1,1-dimethylethyl) dimethylsilyl] oxy. Among them, (1,1 -dimethylethyl), also known as tert-butyl, has a structure of -C (CH < 3), which has a large steric resistance; dimethylsilyl, that is, -Si (CH ₃)₂ - , is connected to the oxygen atom to form this long chain substituent.
    This long chain substituent is connected to the 7 position of the pyridine ring, and the existence of other substituents on the pyridine ring makes the spatial structure and electron cloud distribution of the whole molecule unique, which in turn affects its physical and chemical properties. Thus, the details of the chemical structure of (7R) -4-chloro-7- [ (1,1-dimethylethyl) dimethylsilyl] oxy-6,7-dihydro-5H-cyclopento [b] pyridine-3-formonitrile are given.
    What are the main uses of (7R) -4-Chloro-7- [[ (1,1-dimethylethyl) dimethylsilyl] oxy] -6, 7-dihydro-5H-cyclopenta [b] pyridine-3-carbonitrile
    (7R) -4-chloro-7- [ (1,1-dimethylethyl) dimethylsilyl] oxy-6,7-dihydro-5H-cyclopento [b] pyridine-3-formonitrile, this compound has a wide range of uses. In the field of pharmaceutical research and development, or as a key intermediate. Due to its unique chemical structure, it can be reacted through a series of reactions to build molecular structures with specific biological activities to create new drugs, such as therapeutic drugs targeting specific disease targets. In the field of organic synthesis, it is often used as a starting material or key building block. With its chlorine atoms, siloxy groups and nitrile groups, it can construct complex organic molecules through various organic reactions, such as nucleophilic substitution, coupling reactions, etc., which can be used to synthesize materials with special properties, such as photoelectric materials. It can also provide a foundation for the synthesis of other biologically active or special functional compounds, assist the development of organic synthesis chemistry, and promote the creation and research of new compounds.
    What are the synthesis methods of (7R) -4-Chloro-7- [[ (1,1-dimethylethyl) dimethylsilyl] oxy] -6, 7-dihydro-5H-cyclopenta [b] pyridine-3-carbonitrile
    The synthesis of (7R) -4-chloro-7- [ (1,1-dimethylethyl) dimethylsilyl] oxy-6,7-dihydro-5H-cyclopento [b] pyridine-3-formonitrile has been used for a long time, but the advantages and disadvantages of each method are mutually different, and it needs to be screened in detail.
    One method starts with cyclopentopyridine derivatives, first introduces chlorine atoms at specific positions, and then reacts with (1,1-dimethylethyl) dimethylsilyl reagents to form the target siloxy structure, and the formonitrile group is cleverly constructed in appropriate steps. This process requires precise control of the reaction conditions, temperature, time, and reagent dosage are all key. If the temperature is too high, it may cause side reactions and the product is impure; if the temperature is too low, the reaction will be slow and time-consuming.
    Another method is to build a cyclopentopyridine skeleton first, and reserve a check point for the introduction of chlorine, siloxy, and methonitrile groups. Through a step-by-step reaction, each functional group is introduced in sequence. This method requires strict reaction sequence, and if you make a wrong step, you will lose everything. For example, if the siloxy group is introduced too early, it may affect the subsequent introduction of chlorine atoms or methonitrile groups; if the methonitrile group is not constructed properly, it will also affect the overall product structure and purity.
    Another method is to start from simple raw materials and gradually build complex molecular structures through multi-step reactions. The basic fragments are synthesized first, and then the fragments are spliced together through condensation, substitution and other reactions. However, this path is lengthy, and each step of the reaction needs to be carefully operated. The purification of intermediate products cannot be ignored, otherwise impurities will accumulate and the quality of the final product will be worrying.
    Although there are many ways to synthesize this compound, if you want to obtain a product with high purity and high yield, you must weigh the advantages and disadvantages of each method according to the actual situation, and carefully optimize the reaction conditions to be successful.
    What are the physical properties of (7R) -4-Chloro-7- [[ (1,1-dimethylethyl) dimethylsilyl] oxy] -6, 7-dihydro-5H-cyclopenta [b] pyridine-3-carbonitrile
    (7R) -4-chloro-7- [ (1,1-dimethylethyl) dimethylsilyl] oxy-6,7-dihydro-5H-cyclopento [b] pyridine-3-formonitrile This material has complex and interesting physical properties.
    Looking at its appearance, it is often white to light yellow powder, delicate and uniform, slightly shiny in light, like the light of years precipitation. Its melting point is quite critical, about a specific temperature range, this temperature is the node of the transition from solid to liquid, like the critical point of melting ice and snow, which is of great significance for its treatment under specific process conditions. < Br >
    When it comes to solubility, it has certain solubility characteristics in common organic solvents, such as ethanol and dichloromethane. In ethanol, with a slight increase in temperature, the dissolution rate accelerates, and it gradually disperses and fuses like a fish gets water. In dichloromethane, the solution is clear and transparent after dissolution, just like a mirror. This property is very important in the chemical synthesis and separation purification steps. According to this property, an exquisite process can be designed to achieve the desired effect.
    In terms of density, it is relatively stable. Its value reflects the degree of close arrangement of particles within the material, like a closely arranged soldier's phalanx, giving it a specific weight and volume relationship. In storage and transportation, this physical property is a key factor to consider.
    In addition, its stability is also a major characteristic. It can maintain its inherent structure and properties under normal temperature, pressure and dry environment, just like a stable old man, and is not easily disturbed by the outside world. In case of strong acid and alkali, or extreme conditions of high temperature and humidity, the structure may change. In case of hard ice of fire, it will gradually melt and deform. This characteristic warns that caution is required during storage and use to ensure the constancy of its chemical nature.
    What is the market outlook for (7R) -4-Chloro-7- [[ (1,1-dimethylethyl) dimethylsilyl] oxy] -6,7-dihydro-5H-cyclopenta [b] pyridine-3-carbonitrile
    Nowadays, there are (7R) -4-chloro-7- [ (1,1-dimethylethyl) dimethylsilyl] oxy-6,7-dihydro-5H-cyclopento [b] pyridine-3-formonitrile, and its market prospects are related to many aspects.
    In the field of current pharmaceutical research and development, organic synthesis chemistry is booming, and the creation of many new drug molecules depends on complex organic compounds. ( 7R) - 4-chloro-7- [ (1,1-dimethylethyl) dimethylsilyl] oxy-6,7-dihydro-5H-cyclopento [b] pyridine-3-formonitrile compounds may have unique chemical structures and potential biological activities, and may emerge in the screening of drug lead compounds. Pharmaceutical companies and scientific research institutions spare no effort in the search for new chemical entities. If this compound is proved to have affinity and regulatory activity for specific disease targets, it will attract attention from all parties, and then obtain R & D investment. The market prospect may be bright.
    In the field of materials science, special structural organic compounds are often the cornerstones for the preparation of high-performance materials. (7R) -4-chloro-7- [ (1,1-dimethylethyl) dimethylsilyl] oxy-6,7-dihydro-5H-cyclopento [b] pyridine-3-formonitrile The structural properties of (7R) -4-chloro-7- [ (1,1-dimethylethyl) dimethylsilyl] oxy-6,7-dihydro-5H-cyclopento [b] pyridine-3-formonitrile may endow materials with unique electrical, optical or mechanical properties. For example, in the preparation of organic optoelectronic materials, through rational molecular design and modification, key indicators such
    However, the road to its market is not smooth. Synthesizing this compound may pose technical challenges and cost control may become difficult. If the synthesis process is complicated and the yield is low, the cost will be high and the market competitiveness will be affected. And the market takes time to accept new compounds, and strict safety and effectiveness assessments are required. Only by overcoming technical obstacles can this (7R) -4-chloro-7 - [ (1,1-dimethylethyl) dimethylsilyl] oxy-6,7-dihydro-5H-cyclopento [b] pyridine-3-formonitrile be widely sold in the market, with unlimited prospects.