3 7 Dihydro 5 Iodo 4h Pyrrolo 2 3 D Pyrimidin 4 One
Iodobenzene

3,7-dihydro-5-iodo-4h-pyrrolo[2,3-d]pyrimidin-4-one

Fengxi Chemical

Specifications

HS Code

124809

Chemical Formula C6H4IN3O
Molar Mass 263.02 g/mol
Appearance Solid (usually)
Melting Point Data needed
Boiling Point Data needed
Solubility In Water Limited solubility likely
Solubility In Organic Solvents Soluble in some organic solvents
Density Data needed
Pka Data needed
Stability Stable under normal conditions
Chemical Formula C6H4IN3O
Molecular Weight 261.02
Chemical Formula C6H4IN3O
Molar Mass 261.02 g/mol
Physical State Solid (predicted)
Appearance White to off - white solid (predicted)
Solubility In Water Low (due to its non - polar nature in part)
Solubility In Organic Solvents Soluble in some organic solvents like DMSO, DMF (predicted)
Chemical Formula C6H4IN3O
Molar Mass 261.02 g/mol
Physical State Solid (usually)
Appearance Off - white to yellowish solid
Melting Point N/A (experimental value may vary)
Boiling Point N/A (decomposes before boiling)
Solubility In Water Low solubility in water
Solubility In Organic Solvents Soluble in some polar organic solvents like DMSO
Density N/A (experimental determination required)
Crystal Structure Unknown (without X - ray diffraction study)
Odor Odorless or very faint odor
Packing & Storage
Packing 100g of 3,7 - dihydro - 5 - iodo - 4h - pyrrolo[2,3 - d]pyrimidin - 4 - one in sealed chemical - grade packaging.
Storage Store 3,7 - dihydro - 5 - iodo - 4H - pyrrolo[2,3 - d]pyrimidin - 4 - one in a cool, dry place, away from direct sunlight. Keep it in a tightly sealed container to prevent moisture absorption and exposure to air, which could potentially lead to decomposition. Store it separately from incompatible substances to avoid chemical reactions.
Shipping The chemical "3,7 - dihydro - 5 - iodo - 4h - pyrrolo[2,3 - d]pyrimidin - 4 - one" will be shipped in sealed, appropriately labeled containers. Special handling for chemicals is ensured to maintain integrity during transit.
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3,7-dihydro-5-iodo-4h-pyrrolo[2,3-d]pyrimidin-4-one 3,7-dihydro-5-iodo-4h-pyrrolo[2,3-d]pyrimidin-4-one 3,7-dihydro-5-iodo-4h-pyrrolo[2,3-d]pyrimidin-4-one
General Information
Frequently Asked Questions
What are the chemical properties of 3,7-dihydro-5-iodine-4H-pyrrolido [2,3-d] pyrimidine-4-one?
This is a question about the properties of a chemical substance, which is "3% 2C7-dioxide-5-azole-4H-pyrrolido [2,3-d] pyrimidine-4-amine". This compound has the following chemical properties:
From a structural perspective, its nitrogen-containing heterocyclic structure is quite complex. It is formed by fusing pyrrole rings with pyrimidine rings. This fused ring structure endows the molecule with specific stability and electron cloud distribution characteristics. Nitrogen atoms exist in different hybrid states in the ring, which has a significant impact on the electron cloud density and chemical reactivity of the whole molecule. For example, non-shared electron pairs on nitrogen atoms can participate in many reactions, such as nucleophilic reactions, because they can provide electrons and exhibit nucleophilicity.
In terms of physical properties, since it contains multiple polar atoms and groups, such as nitrogen and oxygen atoms, it is speculated that it has a certain polarity, and its solubility in common organic solvents may be related to polarity. In water, its solubility may exhibit specific performance due to factors such as molecular polarity and hydrogen bonding. Generally speaking, polar organic solvents such as alcohols and ketones have better solubility than non-polar solvents such as alkanes.
From the perspective of chemical activity, the nitrogen atoms and amine groups on its rings are all reactive activity check points. Amine groups are typically alkaline and can neutralize with acids to generate corresponding salts. At the same time, due to the uneven distribution of electron clouds in molecules, the density of electron clouds on some carbon atoms is relatively low, making them vulnerable to attack by nucleophiles and nucleophilic substitution reactions. Under suitable conditions, cyclization reactions, redox reactions, etc. may also occur.
This compound has important application value in organic synthesis, pharmaceutical chemistry and other fields due to its unique chemical structure. It can be used as a key intermediate for the synthesis of more complex compounds with specific biological activities.
What are the common synthesis methods of 3,7-dihydro-5-iodine-4H-pyrrolido [2,3-d] pyrimidine-4-one?
In order to obtain this substance, a specific method needs to be followed. This involves starting with 3% of a certain agent and 2,7-diketone, and then going through a series of steps.
The first step is to put 2,7-diketone in a suitable vessel, and then add an appropriate amount of 3% of the specific agent. The properties of this agent can initiate specific chemical changes. In the meantime, it is necessary to control the temperature moderately and add stirring from time to time to make the two mix evenly and promote the reaction to go forward.
Then, during the reaction process, an intermediate state will be formed. At this time, 5-nitrogen is added, and this nitrogen can interact with the reaction products of the former two in the system to change the direction of the chemical change. When adding nitrogen, the rate should also be paid attention to. If it is too fast or too slow, it may affect the final product.
After that, the addition of 4H and hydrogen is often an active element in the transformation. The addition of 4H can further transform the reaction system and tend to the desired product. This step of the reaction requires quite strict environmental requirements, such as humidity and air pressure, which need to be carefully regulated.
As for the preparation of [2,3-d] quinoline, there is also a method. With specific raw materials, through suitable reaction conditions, such as catalysis, heating and other means, the raw materials can be gradually converted into [2,3-d] quinoline. In this process, the choice of catalyst is very critical, different catalysts, or the difference between the reaction rate and the purity of the product.
As for the subsequent steps of subtracting 4 and removing aldehyde, there are also different ways. Subtracting 4 may require specific reagents to react with it to remove the part of 4. In addition to aldehyde, the common method is either chemical adsorption or reaction with other agents to make the aldehyde into a state that is easy to separate, and then separation techniques, such as distillation, extraction, etc., to obtain a pure final product.
In short, to achieve this synthesis, it is necessary to accurately grasp the conditions of each step of the reaction, the amount and order of reagents, in order to obtain the desired product.
In what fields is 3,7-dihydro-5-iodine-4H-pyrrolido [2,3-d] pyrimidine-4-one used?
Let's look at this equation, where "3% 2C7", or the expression of numerical value, but in common arithmetic, if this "%" is a remainder operation, 3 divided by 2 is 1, which seems to be different from the book "3% 2C7", which is questionable here. "Dioxygen", presumably refers to "carbon dioxide", chemical things are also. "5-dice-4H", "dice", dice also, in the field of chemistry or other sciences, the meaning of this combination is unknown. "To beryllium [2,3-d] quinoline-4-one", this is the name of an organic chemical, which is a nitrogen-containing heterocyclic compound and the like, often used in pharmaceutical chemistry, organic synthesis and other fields.
"To beryllium [2,3-d] quinoline-4-one" in the field of pharmaceutical research and development, can be used as pharmaceutical intermediates. Due to its unique activity, chemists use it to build complex molecular structures to find new compounds with pharmacological activity, or to be promising new drugs for treating diseases. In the field of materials science, it may be able to participate in the preparation of special functional materials. For example, organic optoelectronic materials, with their conjugate structure and electronic properties, affect the optical and electrical properties of materials, and can be used to fabricate Light Emitting Diodes, solar cells and other devices. In organic synthetic chemistry, it is a key synthetic building block. Chemists build more complex molecules based on organic reaction mechanisms and various reaction conditions to expand the variety and application of organic compounds.
What are the market prospects for 3,7-dihydro-5-iodine-4H-pyrrolido [2,3-d] pyrimidine-4-one?
The market prospect of 3% 2C7-dioxy-5-well-4H-pyrrolido [2,3-d] pyrimidine-4-amine that Guanfu inquired about is actually related to many factors, like an intertwined map.
This compound has potential applications in the field of medicine. Looking at the current trend of pharmaceutical research, there is a thirst for innovative drugs, which may become a key component of new therapeutic agents due to their unique chemical structure. If it can demonstrate excellent biological activity, such as high affinity and selectivity of targets for specific diseases, just like the precision of the target, the market prospect may be bright.
In the process of research and development, the difficulty of the synthesis process is an important consideration. If the synthesis step is simple and efficient, the raw materials are easy to obtain and the cost is controllable, just like the smooth road, it will definitely improve its commercial viability. On the contrary, if the synthesis process is like thorns and the cost is high, it may limit its large-scale production and marketing activities.
Furthermore, the situation of market competition cannot be ignored. Looking at the market layout of the same type of compound, if this 3% 2C7-dioxy-5-well-4H-pyrrolido [2,3-d] pyrimidine-4-amine can stand out and have unique advantages. If you win with excellent efficacy or safety, you can win a place in the market.
In addition, regulations and policies are like invisible ropes, which also have a great impact on their market prospects. The rigorous drug approval process is like a lot of barriers, and only if you pass it smoothly can you enter the market. Therefore, you need to always pay attention to the trend of regulations to ensure that the road of compliance with R & D is orderly.
To sum up, the market prospect of 3% 2C7-dioxy-5-well-4H-pyrrolido [2,3-d] pyrimidine-4-amine has both opportunities ahead and challenges ahead. If you can properly handle R & D, competition, and regulatory issues, you may be able to shine in the market. If you don't deal with it properly, you may be like a pearl in the dust, and it will be difficult to show its brilliance.
What are the precautions in the preparation of 3,7-dihydro-5-iodine-4H-pyrrolido [2,3-d] pyrimidine-4-one?
To prepare this product, you need to pay attention to the following things:
First, the material is used accurately. The amount of each material of 3% 2,7-diketone-5-hydrazine-4H-pyrano [2,3-d] pyrimidine-4-one needs to be determined according to the prescription, and the measurement should be carefully weighed. If there is a slight difference, or the product is impure, it will affect the subsequent effect. If the agent is prepared, it is completely wrong, or the drug effect is not good.
Second, the reaction environment is very important. During the reaction, temperature, humidity, and air pressure can all affect the reaction process. If the temperature is too high, or the reaction is too fast, the product will decompose; if the temperature is too low, the reaction will be slow and take a long time. Just like cooking, the heat is not appropriate, and it is difficult to make a good meal. The specific temperature and humidity conditions required for this reaction must be strictly controlled to create a suitable environment.
Third, the reaction equipment must be clean. The utensils used must be clean and free of stains, otherwise impurities will mix in and interfere with the reaction, and the products may contain impure impurities. Just as clean water can raise good seedlings, clean utensils are the foundation for a smooth reaction. Before each use, wash and dry in a suitable way to ensure that no impurities remain.
Fourth, the operation steps are carried out in sequence. The preparation process is complicated and orderly, and must not be reversed. Each step is interconnected, and the effect of the previous step is related to the progress of the next step. If you don't operate in sequence, it will seem chaotic and disorderly, and the reaction may be difficult to succeed, or even cause danger.
Fifth, safety protection should not be ignored. When preparing or involving harmful, flammable, and explosive substances, you should strictly follow safety procedures when operating, wear protective clothing, goggles, gloves, etc., and work in a well-ventilated manner. Like walking on thin ice in the abyss, always be vigilant to keep safe and safe from harm.