5 Diiodophenyl 3 4 4 Hydroxy 3 Iodophenoxy L Alanin
Iodobenzene

5-diiodophenyl)-3-(4-(4-hydroxy-3-iodophenoxy)-l-alanin

Fengxi Chemical

Specifications

HS Code

667429

Chemical Formula C19H19I3N2O5
Molecular Weight 699.08
Appearance Solid (usually)
Melting Point Data may vary
Solubility In Water Low solubility (usually)
Solubility In Organic Solvents May have some solubility in certain organic solvents
Odor Odorless (usually)
Color White to off - white (usually)
Stability Stable under normal conditions
Chemical Formula C15H12I3NO4
Molecular Weight 659.97 g/mol
Appearance Solid (likely white to off - white powder)
Solubility In Water Poorly soluble (due to its non - polar aromatic and iodine - containing structure)
Melting Point Specific value would require experimental determination, but likely in the range where organic compounds with similar structure melt (100 - 200°C approximately)
Boiling Point Decomposes before boiling (due to heat - sensitive nature of organic - iodine bonds)
Density Estimated based on similar organic iodine - containing compounds, around 2 - 3 g/cm³
Odor Odorless or very faint odor (common for non - volatile, non - fragrant organic solids)
Stability Stable under normal conditions, but sensitive to light and heat which can cause decomposition of iodine - containing bonds
Polarity Moderate polarity due to the presence of polar groups like -OH and -COOH along with non - polar aromatic rings
Chemical Formula C19H19I3N2O5
Molar Mass 705.07 g/mol
Appearance Solid (presumably, based on common nature of such compounds)
Solubility In Water Low solubility (expected for a large, non - polar - containing organic molecule)
Logp High (due to presence of large hydrophobic phenyl and iodophenyl groups)
Stability Stable under normal conditions (but may degrade under high heat, strong acids/bases)
Chemical Formula C15H13I3NO4
Molecular Weight 659.98 g/mol
Appearance Solid (presumed, based on typical nature of such compounds)
Solubility In Water Low solubility (expected for a compound with this structure)
Stability Stability depends on storage conditions, may be sensitive to light and air
Packing & Storage
Packing 10 grams of (5 - diiodophenyl)-3-(4-(4 - hydroxy - 3 - iodophenoxy)-L - alanin) in sealed chemical packaging.
Storage Store “(5 - diiodophenyl)-3-(4-(4 - hydroxy - 3 - iodophenoxy)-L - alanin” in a cool, dry place away from direct sunlight. Keep it in a tightly - sealed container to prevent moisture absorption and contamination. Avoid storing near incompatible substances. If possible, store at a controlled temperature, typically around 2 - 8 °C for optimal stability.
Shipping Ship the chemical (5 - diiodophenyl)-3-(4-(4 - hydroxy - 3 - iodophenoxy)-L - alanin) in well - sealed containers. Ensure compliance with hazardous chemical shipping regulations, using appropriate cushioning to prevent breakage during transit.
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5-diiodophenyl)-3-(4-(4-hydroxy-3-iodophenoxy)-l-alanin 5-diiodophenyl)-3-(4-(4-hydroxy-3-iodophenoxy)-l-alanin 5-diiodophenyl)-3-(4-(4-hydroxy-3-iodophenoxy)-l-alanin
General Information
Frequently Asked Questions
What is the chemical structure of this "5- (diiodophenyl) -3- (4- (4-hydroxy-3-iodophenoxy) -L-alanine"
This "5- (diazinyl) -3- (4- (4-fluoro-3-azinoxy) -L-alanine" is one of the organic compounds. Its chemical structure is quite complex, let me tell you in detail.
The main structure of this compound is based on alanine, which is an α-amino acid with amino and carboxyl groups. L-alanine indicates that its configuration is left-handed. On the basis of the alanine structure, there is a complex substituent on one side.
This substituent starts with "5- (diazinyl) -3 -". The diazinyl group is a six-membered heterocyclic structure composed of two nitrogen atoms and four carbon atoms. The two nitrogen atoms are at a specific position on the ring, giving the structure a specific electron cloud distribution and reactivity. The bond between the diazinyl group and the alanine is connected according to the bonding rules of organic chemistry, or is a covalent bond, which maintains the stability of the structure by sharing electron pairs between atoms.
Looking at the "3- (4- (4-fluoro-3-azinyloxy) " part again, "4-fluoro", the fluorine atom has strong electronegativity and is connected to a specific carbon site, which has a great impact on the distribution and polarity of molecular electron clouds, and can significantly change molecular physical and chemical properties. "3-azinyloxy", the azinyl group is also a nitrogen-containing heterocyclic ring, which is connected to the oxygen atom to form an oxygen group, which is then connected to other structures. This long chain of substituents is connected by carbon-carbon bonds, carbon-nitrogen bonds and other covalent bonds to form a complex and orderly structure.
Each atom and group are connected to each other by covalent bonds to construct this unique chemical structure. Differences in the electronegativity of different atoms cause uneven distribution of electron clouds, endowing molecules with specific polarity and reactivity check points, which affect their physicochemical properties, such as solubility, stability, chemical reactivity, etc. This structure may have potential application value in organic synthesis, medicinal chemistry and other fields, or be a key intermediate for new drug development and material synthesis.
What are the main physical properties of "5- (diiodophenyl) -3- (4- (4-hydroxy-3-iodophenoxy) -L-alanine"
This is a rather complex chemical expression, which mainly involves many chemical groups and substances, and contains specific physical properties.
"5- (dipyridyl) -3- (4- (4-quinolinyl-3-pyridyloxy) -L-alanine) " Among them, groups such as pyridyl and quinolinyl give this compound unique properties. Pyridyl groups are nitrogen-containing heterocycles, which have certain basic properties and coordination capabilities. They can participate in many chemical reactions and form complexes with metal ions. The quinolinyl group also contains nitrogen and has a rigid planar structure, which affects the molecular conjugation system and electron cloud distribution, and then affects the optical and electrical properties of the compound.
From the perspective of the overall structure, L-alanine is partially introduced into the chiral center, which makes the compound optically active. Chiral compounds often have different physiological activities in vivo. Due to the chiral recognition ability of many receptors and enzymes in vivo, different enantiomers of different configurations may have different physiological effects.
Furthermore, the numerous aromatic ring structures in the molecule increase the molecular rigidity and stability, and at the same time increase the intermolecular van der Waals force. Pi-π stacking between aromatic rings allows molecules to self-assemble in solid or solution to form a specific ordered structure, which affects material properties such as solubility, melting point, crystallinity, etc. In terms of solubility, the compound contains polar and non-polar parts. The overall solubility may be affected by the polarity of the solvent, and the solubility may be different in polar and non-polar solvents. The melting point may be relatively high due to strong intermolecular forces. Due to the interaction between rigid structures and molecules, the thermal movement of molecules is hindered, and higher energy is required to remove the molecules from the lattice.
This compound has potential application value in materials science, medicinal chemistry and other fields due to the above physical properties. In the field of materials, it can be used to prepare optical and electrical materials; in the field of medicinal chemistry, chiral and special structures may make it a lead compound with specific biological activities.
In which fields is "5- (diiodophenyl) -3- (4- (4-hydroxy-3-iodophenoxy) -L-alanine" used?
"5- (diterpene-based) -3- (4- (4-pentyl-3-terpene-oxy) -L-alanine" This substance is used in many fields such as alchemy practice, alchemy and pharmaceuticals, Qimen Elusion Armor, and machine number.
In alchemy practice, this substance may assist practitioners in reconciling yin and yang in the body. Alchemy practice focuses on the cultivation of human essence and spirit, and pursues the realm of unity between heaven and man, and long-term vision. The characteristics of this substance may optimize the flow of qi and machine in the body of practitioners, help them more smoothly open up meridians, and reach a higher level of practice.
At the time of alchemy and pharmacy, this substance may be a key medicinal guide. Ancient alchemy, designed to refine longevity pills or a good medicine for healing and saving people. The unique chemical structure and properties of this substance may change the medicinal power and efficacy of the pill, making the pill more miraculous, or can cure chronic diseases, or can increase human qi and blood.
The art of Qimen Escaping Armor is arranged in the direction of the five elements of heaven and earth and the gossip. This substance may be placed in a specific position according to its five elements properties to adjust the aura and reverse the situation. Qimen Escaping Armor is used in military operations, travel, etc. When setting up a formation, this substance may play a unique role in helping users seek good luck and avoid danger and control the situation.
In the field of mechanism operations, this substance may be used to enhance the performance of the mechanism. Ancient mechanism techniques are exquisite and involve mechanical transmission, power sources, etc. This substance may be used as a special material to improve the firmness and flexibility of mechanism components, making the mechanism operate more efficiently and durably, such as for the manufacture of automatic defense mechanisms, transportation mechanisms, etc.
What are the synthesis methods of "5- (diiodophenyl) -3- (4- (4-hydroxy-3-iodophenoxy) -L-alanine"
To prepare "5- (dipeptide glycyl) -3- (4- (4-urea-3-peptide glyoxy) -L-alanine", there are many methods of synthesis, each with its ingenuity, and with the changes of the times and the refinement of technology, there are also differences. Today, imitating the ancient classical style of "Tiangong Kaiwu", the approximate method is as follows:
First, you can take suitable raw materials first, and concentrate them in a specific reaction vessel in a delicate ratio. Make the raw materials blend with each other, and allow them to react slowly under mild conditions, either temperature control or pressure regulation. This process requires constant attention to the reaction situation, just like riding a horse on a narrow road. If you are not careful, you will give up all your efforts. If the compounds containing specific groups are combined with each other to form a preliminary intermediate, this intermediate is like the cornerstone of building a tall building, and its structure and properties are crucial.
Second, you can use a specific catalyst to help. Catalysts, like the guide of chemical reactions, can make the reaction path smoother and speed up the reaction process. However, the choice of catalyst and the dosage need to be considered repeatedly. If the catalyst is not selected properly, or the reaction deviates from expectations, many by-products will be produced, which will increase the difficulty of separation and purification.
Third, separation and purification are also key steps. After the reaction is completed, the product is often mixed in many impurities, such as gold panning in sand. It is necessary to use suitable methods, such as extraction, crystallization, chromatography, etc., to carefully separate the target product to make it pure and flawless, in order to meet the requirements of subsequent use. Every step of the operation needs to be careful, such as caring for the delicate stamens, and a slight error may damage the product.
Fourth, during the synthesis process, the control of the reaction environment cannot be ignored. Whether it is the pH of the reaction system or the choice of solvent, it has a profound impact on the success or failure of the reaction and the quality of the product. It is necessary to create a suitable microenvironment so that the reactants can react freely in it, and finally obtain the desired compound.
Synthesis of "5- (dipeptide glycyl) -3- (4- (4-urea-3-peptide glyoxy) -L-alanine" requires careful study in raw material ratio, reaction conditions, catalyst application, separation and purification and environmental control, etc., in order to obtain exquisite methods and obtain high-quality products.
What is the market outlook for "5- (diiodophenyl) -3- (4- (4-hydroxy-3-iodophenoxy) -L-alanine"?
Guanfu "5- (diterpenoid group) -3- (4- (4-pentyl-3-terpenoid oxy) -L-alanine" This product has a promising market prospect today.
Nowadays, in the field of medicine, research is advanced, and the exploration and application of natural ingredients is on the rise. Such compounds containing terpenoid groups, oxygen groups and other structures may have unique pharmacological activities. Terpenoids are famous for their diverse biological activities, and have potential effects in anti-inflammatory, antibacterial, anti-tumor and other aspects. This "5- (diterpenoid) -3- (4- (4-pentyl-3-terpenoid oxy) -L-alanine" has a delicate structure, or the combination of terpenoid and alanine produces specific physiological effects. If its mechanism of action can be clarified, it will be a great help for the development of innovative drugs, and the pharmaceutical market has broad prospects.
Furthermore, in the chemical industry, the demand for fine chemicals is also increasing day by day. Compounds with such complex structures may be used as special additives for coatings, plastics and other industries to improve product performance. For example, adding it to coatings can increase its weather resistance and corrosion resistance; adding it to plastics can optimize its mechanical properties, so it also has opportunities for development in the chemical market.
However, the road to its market is not smooth. Synthesis of this compound may require complex processes and high costs, which is an obstacle to promotion. And market awareness still needs to be improved, and it needs a lot of experiments and demonstrations to prove its effectiveness and safety before it can be widely recognized in the market.
Overall, the market prospect of "5- (diterpenoid) -3- (4- (4-pentyl-3-terpenoid-oxy) -L-alanine" is promising, but it also needs to solve many problems in order to navigate the market.