5 Iodo 7 2 C Methyl Beta D Ribofuranosyl 7h Pyrrolo 2 3 D Pyrimidin 4 Amine

5-Iodine-7- (2-C-methyl - β - D-furan-ribosyl) -7H-pyrrolido [2,3-d] pyrimidine-4-amine is a complex organic compound. To understand its chemical structure, its name needs to be analyzed first. " 5-Iodine ", shown in the 5 position of the pyrimidine ring with iodine atom substitution;" 7- (2-C-methyl - β - D-furan ribosyl) ", meaning that the 7 position is connected with 2-C-methyl - β - D-furan ribosyl group, this ribosyl group is a sugar structure, with furan ring, and there is methyl substitution on the 2 carbon atom, β-D configuration determines its spatial orientation;" 7H-pyrrolido [2,3-d] pyrimidine ", Ming molecule contains pyrrolido pyrimidine fused heterocyclic ring, this ring is the core structure of the compound , 7H means the relevant substitution at the 7-position hydrogen atom; "4-amine" refers to the amino substitution at the 4-position.
Its chemical structure, the core is pyrrolido [2,3-d] pyrimidine fused ring, which is like the cornerstone of a building. 5-Position iodine atom, like a special sign hanging outside the building; 7-position 2-C-methyl - β - D-furan ribosyl group, such as a unique branch extending from the cornerstone, carrying the characteristics of sugar structure; 4-position amino group, adding reactive check point to the molecule, such as the special entrance of the building, leading to many chemical reactions. This structure is complex and delicate, and the parts are interdependent, which together determine the physical and chemical properties of the compound.

5-Iodo-7- (2-c-methyl-beta-d-ribofuranosyl) -7h-pyrrolo [2,3-d] pyrimidin-4-amine is an organic compound. Its main uses are quite extensive.
In the field of pharmaceutical research and development, this compound may have potential pharmacological activity. Its unique structure may act on specific biological targets, and it is expected to become a lead compound for the treatment of certain diseases. For example, after in-depth research and modification, it may be used in the creation of anti-tumor drugs. Because the growth and proliferation process of tumor cells involves many complex biochemical reactions, the structural characteristics of this compound may interact with tumor-related proteins, enzymes, etc., thereby inhibiting the growth and spread of tumor cells.
In the field of biochemical research, it can be used as a tool compound. By studying its interaction with biological macromolecules, researchers can gain a deeper understanding of the molecular mechanism in living organisms. For example, exploring its binding mode with nucleic acids can enhance the understanding of basic biological processes such as gene expression regulation and DNA replication. This helps to reveal the mysteries of life activities and lay a solid foundation for subsequent biological research.
In the field of organic synthesis, its complex structure and characteristic groups can provide organic synthesis chemists with novel synthesis ideas and challenges. By synthesizing such compounds, chemists can develop and optimize new synthesis methods and strategies to improve the technical level of organic synthesis. By ingeniously designing the reaction route, the efficient synthesis of the compound and its analogs is achieved, providing a sufficient material basis for further research and application.

To prepare 5-iodo-7- (2-c-methyl-β-D-ribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidin-4-amine, the method is as follows:
First take an appropriate amount of starting materials containing specific groups. This raw material needs to be carefully selected and of high quality. In a clean reaction vessel, mix the starting material with a specific reagent in an appropriate proportion. The choice of reagents is a matter of success and failure, and it should be done with caution.
Subsequently, adjust the reaction temperature, which is a key step. Slow down the heat to slowly raise the temperature to a suitable range, during which close attention should be paid to temperature changes, any difference or reaction deviation. After reaching a suitable temperature, maintain stability and make the reaction proceed smoothly.
When reacting, it may be necessary to stir to fully contact the reactants and accelerate the reaction process. And operate in an inert gas atmosphere to prevent the raw materials and products from being oxidized.
After the reaction is completed, the product is precipitated from the reaction system by delicate separation methods, such as column chromatography or recrystallization. The operation needs to be meticulous to avoid product loss. Through this series of steps, the product of 5-iodo-7- (2-c-methyl-β-D-ribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidin-4-amine can be obtained. The whole process is complicated, and the experimenter needs to be skilled and attentive to ensure a smooth reaction and obtain a pure product.

5-Iodo-7- (2-c-methyl-beta-d-ribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidin-4-amine is an organic compound whose physical properties are critical to its application in many fields.
Looking at its morphology, under normal circumstances, this compound is mostly in the form of fine powder, with a fine texture, like early winter snow, with uniform and fine particles. This morphology allows it to disperse more evenly when mixed with other substances, thus affecting the reaction process and product characteristics.
In terms of color, it often shows a white color, pure and flawless, such as the snow on the top of a mountain that is not stained with dust. White color not only reflects its high purity, but also is of great significance in some application scenarios where color is strictly required.
Solubility is also one of the important physical properties. In water, its solubility is poor, just like a stubborn stone entering water, and it is difficult to melt. Due to the many hydrophobic groups in the molecular structure, it is difficult for water molecules to interact with it. However, in organic solvents such as dimethyl sulfoxide (DMSO), it can show good solubility, just like ice and snow in the warm sun, and gradually melt. This characteristic determines its choice of solvent in experimental operation and industrial production.
Melting point is also a physical property that cannot be ignored. After determination, the melting point of this compound is in a certain temperature range. When the temperature rises to the melting point, it will freeze into water and change from solid to liquid. The melting point value provides an important basis for its identification and purity judgment. The higher the purity, the closer the melting point is to the theoretical value.
In addition, the density of this compound, although the value is relatively fixed, plays a role in the process of material separation and mixing. Its density characteristics determine its position in liquid systems of different densities, which is helpful for separation and purification operations.
In summary, the morphology, color, solubility, melting point and density of 5-iodo-7- (2-c-methyl-beta-d-ribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidin-4-amine are of great significance to its research, application and production, just like a cornerstone in a tall building.

5-Iodine-7- (2-C-methyl - β - D-furan-ribosyl) -7H-pyrrolido [2,3-d] pyrimidine-4-amine is a rather complex chemical substance. Looking at its market prospects, it is very multi-faceted.
In the field of medicine, such compounds containing specific ribosyl and pyrimidine structures are often concerned by drug development. Because of its unique structure, or can interact with specific targets in organisms, it may have potential value in the development of antiviral and antitumor drugs. The current market demand for antiviral and anti-tumor drugs is huge and continues to grow. If this compound can demonstrate good pharmacological activity and safety through in-depth research and development, it is very likely to gain a place in the market, and the prospects are quite promising.
However, in actual marketing activities, there are also many challenges. First, the drug research and development process is long and expensive. From basic research, pre-clinical trials to clinical trials, a lot of manpower, material resources and time are required. If the compound encounters problems such as poor stability and low bioavailability during the research and development process, it may hinder the research and development process and consume more resources. Secondly, the market competition is fierce. Many pharmaceutical companies in the pharmaceutical field are committed to the research and development of new drugs. Compounds with similar structures or functions may already be in different stages of research and development. To stand out, they need to have significant advantages.
Looking at other fields such as chemical industry, or because of its special structure, it can be used as a key intermediate in the synthesis of some fine chemical products. With the development of the fine chemical industry, the demand for characteristic intermediates may increase. If it can be effectively developed for application in this field, it can also open up a certain market space. However, the chemical industry has strict requirements on compound purity and mass production feasibility. It is necessary to overcome relevant technical problems in order to achieve large-scale production and application.
Overall, there are opportunities and challenges in the market prospects of 5-iodine-7- (2-C-methyl - β - D-furan-ribosyl) -7H-pyrrolio [2,3-d] pyrimidine-4-amine, and in-depth research and technological breakthroughs are required to fully explore its market potential.