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What is the chemical structure of methyl 1- (phenylsulfonyl) -1H-pyrrolo [2,3-b] pyridine-3-carboxylate?
This is the chemical structure analysis of "methyl 1- (benzenesulfonyl) -1H-pyrrolido [2,3 -b] pyridine-3-carboxylic acid ester". Looking at its name, its structural composition can be deduced. "Methyl" is a group -CH < unk > containing one carbon atom and three hydrogen atoms, which is often one of the ester groups in ester compounds. "1- (benzenesulfonyl) ", where "benzenesulfonyl" is the structure of phenyl linked to sulfonyl (-SO < unk > -), that is, C < unk > H < SO < unk > -, and is connected to the No. 1 position of the main structure. " 1H-pyrrole [2,3-b] pyridine ", this is a fused heterocyclic structure, formed by fusing pyrrole ring with pyridine ring," [2,3-b] "shows the positional relationship between the fused two rings," 1H "table 1 has a hydrogen atom." 3-carboxylate ", indicating that there is a carboxylic acid ester group connected at the 3rd position, and the" methyl "at the beginning is combined, which can be known as -COOCH. In general, this compound uses 1H-pyrrole [2,3-b] pyridine as the core skeleton, benzenesulfonyl at the 1st position, and methyl carboxylate at the 3rd position, thus constituting its chemical structure.
What are the main uses of methyl 1- (phenylsulfonyl) -1H-pyrrolo [2,3-b] pyridine-3-carboxylate?
Methyl 1- (benzenesulfonyl) -1H-pyrrolido [2,3-b] pyridine-3-carboxylic acid ester, which has a wide range of uses. In the field of medicinal chemistry, it is often used as an intermediate in organic synthesis to help build new drug molecular architectures. Due to its unique chemical structure and activity, it can be modified by various chemical reactions to synthesize compounds with specific biological activities, paving the way for the development of new drugs.
In the field of materials science, or involved in the creation of organic optoelectronic materials. Its structure gives the material unique electrical and optical properties, which is expected to be used in organic Light Emitting Diodes, solar cells and other devices to improve their performance and efficiency.
In scientific research and exploration, as a key raw material for researchers to deeply study the properties and reaction mechanisms of pyrrolidine compounds, expand the boundaries of organic chemistry knowledge, and lay the foundation for innovation and development in related fields. With its multi-faceted uses, this compound has important value in chemical industry, scientific research and many other fields, and is like a key to opening the door to many technologies.
What are the synthesis methods of methyl 1- (phenylsulfonyl) -1H-pyrrolo [2,3-b] pyridine-3-carboxylate?
The method of synthesizing methyl 1- (phenylsulfonyl) -1H-pyrrolo [2,3-b] pyridine-3-carboxylate has various paths. First, the target molecule can be constructed by a multi-step reaction starting from a substrate containing pyridine and pyrrole structures. Initially, a suitable pyridine derivative is selected and a suitable substituent is introduced at a specific position in the pyridine ring. This step requires fine control of the reaction conditions, such as temperature, catalyst type and dosage, etc., to guide the desired substitution check point.
Then, pyrrole derivatives are reacted with it, or reactions such as nuclear substitution and cyclization condensation are used to construct the parent nucleus of pyrrolido-pyridine. In this process, the reaction solvent needs to be carefully selected, and different solvents have a significant impact on the reaction rate and selectivity.
Furthermore, the introduction of phenyl sulfonyl groups can be used to sulfonate reagents to interact with the aforementioned intermediates under a suitable reaction environment. This step requires very high reactivity and selectivity, and requires precise regulation of reaction parameters.
Or, the strategy of constructing some key structural fragments first and then coupling them through fragments can be considered. First, fragments containing pyridine, pyrrole and carboxyl esters are synthesized separately, and then the fragments are spliced through ingenious organic reactions, such as coupling reactions catalyzed by transition metals. This strategy can effectively control the reaction process and improve the synthesis efficiency, but the requirements for fragment design and synthesis are also quite high.
Synthesis of methyl 1- (phenylsulfonyl) -1H-pyrrolo [2,3-b] pyridine-3-carboxylate, according to the characteristics of the substrate, reaction conditions and operability and other factors to choose the optimal synthesis path to achieve high efficiency and high purity synthesis goals.
What are the physical properties of methyl 1- (phenylsulfonyl) -1H-pyrrolo [2,3-b] pyridine-3-carboxylate?
Methyl 1- (benzenesulfonyl) -1H-pyrrolido [2,3-b] pyridine-3-carboxylic acid ester, this is an organic compound. Its physical properties are of great interest.
Looking at its appearance, under room temperature and pressure, it mostly appears as a solid state, which is caused by intermolecular forces and structural properties. The melting point of this compound is an important physical property. The melting point is determined by the chemical bonds and interatomic interactions in the molecular structure. After many experimental measurements and theoretical calculations, its melting point may be in a specific temperature range, which is related to the interaction between molecules and hydrogen bonds.
Furthermore, solubility is also a key physical property. In organic solvents, such as common ethanol, dichloromethane, etc., it may exhibit good solubility. This is because the organic solvent and the compound molecules can form van der Waals forces, hydrogen bonds and other interactions, which promote the occurrence of the dissolution process. However, in water, its solubility may not be good, because its molecular structure is strong in hydrophobicity, and the interaction with water molecules is weak.
In addition, the density of the compound is also a category of physical properties. Its density is related to the molecular weight and the degree of molecular packing. With accurate measurement methods, the specific value of its density can be obtained, which is of great significance in many chemical application scenarios, such as material separation, reaction system design, etc.
In summary, the physical properties of methyl 1- (benzenesulfonyl) -1H-pyrrolo [2,3 - b] pyridine-3-carboxylic acid esters, such as appearance, melting point, solubility, density, etc., are determined by the nature of their molecular structure, and play an indispensable role in chemical research and practical application fields.
What is the market outlook for methyl 1- (phenylsulfonyl) -1H-pyrrolo [2,3-b] pyridine-3-carboxylate?
Methyl 1- (benzenesulfonyl) -1H-pyrrolido [2,3-b] pyridine-3-carboxylate, this compound is like a star in the sky in today's market prospects, and its brilliance is waiting to be carefully observed.
In the current field of pharmaceutical and chemical engineering, innovative drug research and development is like a thousand sails racing, and this compound may emerge in the meantime. In the process of drug synthesis, its unique molecular structure is like the key to opening the door to treasure. The exploration of many new targeted drugs requires such novel compounds as cornerstones, which may pave a new way for the creation of anti-cancer, anti-inflammatory and other drugs, and the market potential cannot be underestimated.
In the field of materials science, the progress of science and technology is like a river. Due to its own structural characteristics, this compound may become a key raw material for the preparation of high-performance organic materials. For example, the innovation of optoelectronic materials, the demand for compounds with special optoelectronic properties is increasing, and it may be able to find a place in this booming field, shining in cutting-edge technologies such as flat panel displays and solar cells.
However, its market prospects are not smooth sailing, just like a boat in the waves. The complexity of the synthesis process is like a roadblock, increasing production costs and restricting its large-scale production and application. And similar competitive compounds are also standing like a forest. If they want to win the market, they need to overcome many difficulties and obstacles. However, if we can break through the technical shackles, optimize the synthesis process, and improve product quality, this compound will surely be like a dragon, swimming in the blue ocean of the market, shining brightly in the fields of medicine and materials, contributing to the progress of the industry and winning a broad market prospect.