2 Deoxy 5 Iodocytidine
Iodobenzene

2 Deoxy 5 Iodocytidine

Fengxi Chemical

Specifications

HS Code

566297

Chemical Formula C9H12IN3O4
Molecular Weight 365.11
Appearance White to off - white solid
Solubility Soluble in some organic solvents
Melting Point Typically in a certain temperature range
Pka Specific pKa value related to its acidic/basic nature
Logp A value indicating lipophilicity
Stability Stable under certain conditions, may degrade under others
Uv Vis Absorption Absorbs light at specific wavelengths
Chemical Formula C9H12IN3O4
Molar Mass 367.11 g/mol
Appearance Solid
Solubility Soluble in some organic solvents
Melting Point Specific value would require research
Pka Values depend on functional groups, need research
Density Data would need to be sourced
Stability Stable under proper storage conditions
Chirality May have chiral centers depending on structure
Chemical Formula C9H12IN3O4
Molar Mass 367.114 g/mol
Appearance White to off - white solid
Melting Point Typically in a certain range (data may vary, e.g., around 180 - 190 °C)
Solubility Soluble in some polar solvents like DMSO, less soluble in non - polar solvents
Pka There are relevant pKa values related to its functional groups (data may need precise experimental determination)
Stability Stable under normal storage conditions, but may degrade upon exposure to light, heat, or certain reactive substances
Crystal Structure Has a specific crystal lattice structure determined by X - ray crystallography
Uv Vis Absorption Absorbs light at specific wavelengths in the ultraviolet - visible spectrum
Chirality May possess chiral centers, and exist in enantiomeric forms
Chemical Formula C9H12IN3O4
Molecular Weight 367.114
Appearance Solid
Melting Point 189 - 191 °C
Solubility In Water Slightly soluble
Purity Typically high purity in research - grade products
Cas Number 1032-65-1
Storage Conditions Store at -20°C
Stability Stable under proper storage conditions
Category Nucleoside analogue
Packing & Storage
Packing 10 g of 2'-deoxy-5-iodocytidine packaged in a sealed, chemical - resistant vial.
Storage 2'-Deoxy-5-iodocytidine should be stored in a cool, dry place, away from direct sunlight and heat sources. Keep it in a tightly sealed container to prevent moisture absorption and exposure to air. Ideal storage temperature is typically around 2 - 8°C in a refrigerator. This helps maintain its chemical stability and integrity over time.
Shipping 2'-deoxy - 5 - iodocytidine, a chemical, is shipped in accordance with strict hazardous materials regulations. Packaged securely to prevent breakage, it's transported by carriers trained in handling such substances, ensuring safe delivery.
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2'-deoxy-5-iodocytidine 2'-deoxy-5-iodocytidine 2'-deoxy-5-iodocytidine
General Information
Frequently Asked Questions
What is the chemical structure of -deoxy-5-iodocytidine?
2% 27-deoxy-5-iodocytidine is a kind of organic compound. Its chemical structure is unique, containing deoxyribose, cytosine bases and iodine atoms.
As far as its structure is concerned, deoxyribose is the glycosyl part. This glycosyl is formed by the loss of 2% 27 hydroxyl groups in ribose, so it is called 2% 27-deoxyribose. It plays an important role in supporting and connecting nucleic acid structures.
Cytosine base is a nitrogen-containing heterocyclic structure, which is connected to the 1% 27 carbon atoms of deoxyribose through glycoside bonds. Cytosine belongs to the pyrimidine group of bases and is of great significance for the transmission and expression of genetic information. The 5-iodine atom is attached to the 5-position of the cytosine base. The introduction of the iodine atom greatly changes the physical and chemical properties of the compound. The iodine atom has a large atomic radius and electronegativity, which affects the spatial structure, polarity and reactivity of the molecule.
The chemical structure of 2% 27-deoxy-5-iodine cytidine is composed of 2% 27-deoxy ribose, cytosine base and 5-iodine atom. This unique structure makes it show potential application value in the fields of medicine, biochemistry, etc., such as in the development of antiviral and anti-tumor drugs, and may play an important role.
What are the main uses of 2 '-deoxy-5-iodocytidine?
2% 27-deoxy-5-iodocytidine is a particularly important compound. Its main uses are widely involved in medicine, scientific research and many other fields.
In the field of medicine, this compound is often used in the development of antiviral drugs. It can effectively interfere with the replication process of viruses due to its unique molecular structure. For example, in the study of some DNA viruses, 2% 27-deoxy-5-iodocytidine can be embedded in the DNA chain of the virus, hindering its normal synthesis and replication, thereby inhibiting the proliferation of viruses and providing a key material for the creation of antiviral drugs.
In the field of scientific research, 2% 27-deoxy-5-iodocytidine also plays an important role. First, it can be used as a key component of nucleic acid probes. With its special properties of iodine atoms, the probe can show higher sensitivity and specificity when detecting nucleic acid sequences, helping researchers to detect specific gene fragments more accurately. Second, in cell biology research, this compound can be used to explore the mechanism of nucleic acid metabolism in cells. By observing the uptake, metabolism of 2% 27-deoxy-5-iodocytidine and its impact on the cell cycle, scientists can gain a deeper understanding of the mystery of cellular nucleic acid metabolism.
In conclusion, 2% 27-deoxy-5-iodocytidine, with its unique structure and properties, is of great value in the journey of pharmaceutical research and development and scientific research, and contributes to human beings' fight against diseases and enhance their understanding of life sciences.
What is the synthesis method of 2 '-deoxy-5-iodocytidine?
The synthesis of 2% 27-deoxy-5-iodocytidine is a key issue in the field of organic synthesis. To obtain this compound, the path of chemical synthesis is often followed. The method is roughly as follows:
Starting material, often taking cytidine or its derivatives. Prior to the 2% 27-hydroxy group of cytidine, it is protected by an appropriate protective base to prevent it from participating unnecessarily in the subsequent reaction and causing the reaction direction to deviate from expectations. This protective step is crucial to ensure the accuracy of the reaction.
Then, for the 5-position of cytidine, the technique of iodization is applied. Various iodizing reagents can be used, such as iodine elementals supplemented with specific catalysts, or some active iodized salts. This iodization reaction requires careful regulation of reaction conditions, such as temperature, reaction duration, and proportion of reactants. If the temperature is too high, it may cause side reactions; if the duration is insufficient, the iodization will be incomplete.
After successful iodization of 5-bit, remove 2% of the 27-bit protecting group. The deprotection step requires the appropriate deprotection reagent and conditions according to the characteristics of the selected protecting group. This process needs to ensure that the deprotection reaction is efficient and does not damage the formed 5-iodide structure.
During the entire synthesis process, the products of each step of the reaction need to be carefully separated and purified. Commonly used methods include column chromatography, recrystallization, etc. Through this procedure, a high purity of 2% 27-deoxy-5-iodocytidine can be obtained. Although every step of the synthesis process needs to be handled carefully, following this orderly method can achieve the purpose of synthesizing the target compound.
2 '-deoxy-5-iodocytidine What are the precautions during use?
For 2 '-deoxy-5-iodocytidine, many matters need to be paid attention to when using it. This is a fine compound with unique chemical properties and is the first to be safe when used. Because of its certain chemical activity, be sure to wear suitable protective equipment when exposed, such as gloves, goggles, etc., to prevent it from touching the skin and eyes and causing injury to the body.
In addition, its storage is also exquisite. It should be placed in a dry, cool and well-ventilated place, protected from heat and light, so as to maintain its chemical stability and prevent it from deteriorating, so as to maintain its due effect.
During use, the weighing must be accurate. The dosage of this compound often has a great impact on the experimental results or application results. A little difference may lead to false results. Therefore, accurate weighing equipment should be used, and the dosage should be strictly controlled according to the needs of the experiment or application.
The use environment should not be underestimated. It is necessary to ensure that the operating environment is clean and free of excessive impurities and dust to prevent contamination of this compound and then interfere with its normal use. And the operation process should follow the established norms and procedures, and must not act recklessly.
Because of its biological activity, it is more prudent when applying biological experiments. It is necessary to know its potential impact on the experimental biological system in detail, consider the possible situation in advance, and formulate countermeasures in order to achieve the intended purpose without accident. In short, with 2 '-deoxy-5-iodocytidine, all the details are crucial to success and cannot be ignored.
What is the market outlook for 2 '-deoxy-5-iodocytidine?
2% -deoxy-5-iodocytidine is an important compound in the field of medicinal chemistry. It is especially crucial in the field of antiviral drug research and development. The prospect of the current market of Guanfu can be said to be quite potential.
In the process of antiviral research, many viruses are raging and endangering human health. Such as herpes virus, it poses a serious threat to human life and health. With its unique chemical structure, 2% -deoxy-5-iodocytidine can effectively inhibit the replication process of viruses. Its mechanism of action is that it can accurately incorporate the DNA strand of the virus, and then stop the DNA synthesis of the virus, so as to achieve the effect of antiviral. This characteristic makes it a high-profile research object in the antiviral drug research and development market.
In terms of market demand, the incidence of viral infectious diseases is quite high worldwide and is on the rise. Both developed and developing countries have a strong demand for highly effective antiviral drugs. 2% -deoxy-5-iodocytidine has significant antiviral activity and will be able to meet these market demands. If pharmaceutical companies can successfully develop antiviral drugs based on it, they will be able to occupy a place in the market and reap considerable economic benefits.
Furthermore, research on it is also becoming increasingly in-depth in the field of scientific research. Many scientific research teams are involved in it to explore more potential pharmacological activities. With the advancement of research, it may be able to discover its application value in the treatment of other diseases, such as adjuvant treatment of certain tumor diseases. This will further expand the market prospect of 2% -deoxy-5-iodocytidine, making it more widely used and shining brightly in the future pharmaceutical market.