1 3 2 Dioxaborolane 2 3 Chloro 5 Iodophenyl 4 4 5 5 Tetramethyl
Iodobenzene

1 3 2 Dioxaborolane 2 3 Chloro 5 Iodophenyl 4 4 5 5 Tetramethyl

Fengxi Chemical

Specifications

HS Code

625502

Chemical Formula C12H17BClIO2
Molecular Weight 364.43
Appearance Solid (Typical)
Melting Point Data may vary
Boiling Point Data may vary
Density Data may vary
Solubility Solubility characteristics depend on solvents
Purity Can be specified by manufacturer
Cas Number Data required from specific sources
Storage Conditions Should be stored in a cool, dry place
Chemical Formula C12H15BClIO2
Molecular Weight 366.41
Appearance Solid (likely, based on similar compounds)
Solubility Soluble in organic solvents like dichloromethane, toluene (common for similar boron - containing aromatic compounds)
Stability Stable under normal conditions, but sensitive to strong oxidizing agents and moisture
Reactivity Reactive in cross - coupling reactions such as Suzuki - Miyaura coupling due to the presence of the boron - containing moiety and halogen atoms
Chemical Formula C12H17BClIO2
Molecular Weight 366.53
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, toluene (typical for such organoboron compounds)
Stability Air - and moisture - sensitive (common for borolane derivatives)
Reactivity Reactive in cross - coupling reactions (e.g., Suzuki - Miyaura coupling due to the presence of boron and halide groups)
Chemical Formula C12H15BClIO2
Molecular Weight 364.41
Appearance Solid (likely)
Melting Point Data may vary, check literature
Boiling Point Data may vary, check literature
Solubility Solubility characteristics in different solvents would need literature research
Density Data may vary, check literature
Flash Point Data may vary, check literature
Purity Can be specified as a % value in commercial products, check product specs
Stability May be sensitive to air, moisture etc., check literature
Packing & Storage
Packing 100g of 2-(3 - chloro - 5 - iodophenyl)-4,4,5,5 - tetramethyl -1,3,2 - dioxaborolane in sealed vial.
Storage 1,3,2 - dioxaborolane, 2-(3 - chloro - 5 - iodophenyl)-4,4,4,5,5 - tetramethyl - should be stored in a cool, dry place, away from heat and ignition sources. Keep it in a tightly - sealed container to prevent exposure to air and moisture, which could potentially lead to decomposition or reaction. Store it separately from incompatible substances, following safety regulations for handling halogen - containing and borane - based chemicals.
Shipping 1,3,2 - dioxaborolane, 2 - (3 - chloro - 5 - iodophenyl)-4,4,5,5 - tetramethyl - is shipped in accordance with strict chemical transport regulations. Packaged securely to prevent leakage, transported in appropriate containers, and handled with care for safety.
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1,3,2-dioxaborolane, 2-(3-chloro-5-iodophenyl)-4,4,5,5-tetramethyl- 1,3,2-dioxaborolane, 2-(3-chloro-5-iodophenyl)-4,4,5,5-tetramethyl- 1,3,2-dioxaborolane, 2-(3-chloro-5-iodophenyl)-4,4,5,5-tetramethyl-
General Information
Frequently Asked Questions
What are the physical properties of 1,3,2-dioxaborane, 2- (3-chloro-5-iodophenyl) -4,4,5,5-tetramethyl-
The material properties of 1% 2C3% 2C2-dioxetane, 2- (3-chloro-5-pyrimidinyl) -4% 2C4% 2C5% 2C5-tetramethyl-are as follows:
This compound has specific properties due to its unique chemical structure. From the perspective of physical properties, it may be a solid state under normal conditions, and the specific melting point and boiling point vary depending on the fine structure. Differences in the bonding mode between atoms and the electronegativity of atoms within the molecule cause differences in molecular polarity or affect its solubility in different solvents. Generally speaking, due to its various functional groups, it may exhibit different dissolution tendencies in polar and non-polar solvents.
Chemically, 3-chloro-5-pyrimidinyl groups interact with 1% 2C3% 2C2-dioxane and tetramethyl structures. The activity of chlorine atoms may make the compound prone to nucleophilic substitution reactions, and nucleophilic reagents can attack the carbon atoms attached to the chlorine atoms, causing chlorine to be replaced. Pyrimidine rings are aromatic and can participate in a variety of aromatic-specific reactions, such as electrophilic substitution reactions. However, the structure of dioxane may undergo ring-opening reactions under specific conditions, expanding the molecular structure and participating in more complex reactions. Tetramethyl groups can use their electronic effects to affect the overall reactivity and stability of the molecule, or increase the molecular steric resistance, which has an effect on the reaction selectivity.
What are the chemical synthesis methods of 1,3,2-dioxaborane, 2- (3-chloro-5-iodophenyl) -4,4,5,5-tetramethyl-
There are many chemical synthesis methods for 1% 2C3% 2C2-dioxane, 2- (3-chloro-5-bromobenzyl) -4% 2C4% 2C5% 2C5-tetramethyl -. The following is a detailed description.
First, through the selection and reaction of starting materials. With a compound containing a specific halogenated benzyl structure and a raw material containing a dioxane skeleton, under the action of a suitable base and catalyst, a nucleophilic substitution reaction occurs in an organic solvent. This process is like two dancers, on a specific stage (solvent), under the guidance of the conductor (catalyst and base), precisely combine. For example, selecting a suitable halogenated benzyl halide, together with the corresponding dioxane derivatives, in a solvent such as toluene, using potassium carbonate as a base and cuprous iodide as a catalyst, heating reaction can gradually build the target structure.
Second, the intermediate product can be modified. First synthesize the intermediate product containing part of the target structure, and then improve it by means of functional group conversion. Like building a castle, first build the main frame, and then refine the details. For example, first prepare intermediates with similar benzyl groups but different halogen atoms, and then introduce the required chlorine and bromine atoms through a halogen exchange reaction to achieve the synthesis of the target product.
Third, adopt a step-by-step construction strategy. Starting from simple basic raw materials, such as common alcohols, aldides, ketones, etc., through multi-step reactions, dioxapentane rings are first built, then benzyl groups are introduced, and chlorine and bromine atoms are gradually introduced on the benzyl groups. This process is like drawing a precise picture, stroke by stroke, step by step, and finally a complete picture is drawn. It is necessary to pay attention to the precise control of the reaction conditions at each step, such as temperature, reaction time, proportion of reactants, etc., to obtain the target product of ideal yield and purity.
What are the applications of 1,3,2-dioxaborane, 2- (3-chloro-5-iodophenyl) -4,4,5,5-tetramethyl-in organic synthesis?
1% 2C3% 2C2-dioxapentane, 2- (3-chloro-5-thiophenyl) -4% 2C4% 2C5% 2C5-tetramethyl-in organic synthesis, this substance is widely used. In the field of pharmaceutical chemistry, it is often used as a key intermediate to help create many drugs. For example, in the development of specific antiviral drugs, with its unique chemical structure, it can effectively participate in the reaction, build the core part of drug activity, and open up new paths for drug research and development.
In the field of materials science, it also has significant uses. It can be modified by specific reactions and integrated into polymer material systems to improve material properties. Such as improving the thermal stability and mechanical strength of materials, or endowing materials with special optical and electrical properties, so that materials can be used in many fields such as electronic devices and optical materials.
In the field of fine chemicals, it is an important raw material for the synthesis of various fine chemicals. It can be used to prepare fine products such as fragrances and additives, endowing products with unique aroma or excellent properties, and meeting the needs of different industries.
In summary, 1% 2C3% 2C2-dioxane, 2- (3-chloro-5-thiophenyl) -4% 2C4% 2C5% 2C5-tetramethyl are indispensable in many fields of organic synthesis, playing a significant role in promoting the continuous development and progress of related industries.
What are the storage conditions for 1,3,2-dioxaborane, 2- (3-chloro-5-iodophenyl) -4,4,5,5-tetramethyl-?
Storage conditions for 1% 2C3% 2C2-dioxapentanone, 2- (3-chloro-5-thiophenyl) -4% 2C4% 2C5% 2C5-tetramethyl -, this is the content of chemical substances. The following is answered in classical Chinese form:
1% 2C3% 2C2-dioxapentanone and 2- (3-chloro-5-thiophenyl) -4% 2C4% 2C5% 2C5-tetramethyl This substance, the temperature and humidity of the first environment. It should be placed in a cool, dry place away from direct sunlight. Sunlight can promote its chemical reactions and cause it to deteriorate.
As for the humidity, too high will easily cause deliquescence, and too low or cause its physical properties to change. Generally speaking, the humidity should be controlled between [X]% and [X]%. Temperature is also critical, and it should be in the range of [X] ° C to [X] ° C. Excessive temperature, molecular movement will intensify, or cause structural changes; too low temperature, or affect its stability.
In addition, the storage place should be well ventilated, avoiding other miscellaneous places to prevent interaction. These two types of substances may have special chemical activities, and in case of incompatible substances, they may cause violent reactions and endanger safety.
And it needs to be properly sealed to prevent contact with the air. Oxygen, water vapor, etc. in the air can interact with the material and damage its quality. Therefore, the sealing device should be selected as a material adapter to ensure its chemical stability. In this way, it is necessary to store these two types of substances and preserve their characteristics for future use.
What is the market price of 1,3,2-dioxaborane, 2- (3-chloro-5-iodophenyl) -4,4,5,5-tetramethyl-
1% 2C3% 2C2-dioxacyclopentanone, 2- (3-bromo-5-chlorophenyl) -4% 2C4% 2C5% 2C5-tetramethyl-this item is in the market, what is the price of it? This question is similar to what is involved in "Tiangong Kaiwu". It is necessary to consider various factors in order to know its approximation.
The first thing to think about is the production of this item. If the production method is difficult, the materials used are scarce and difficult to collect, or exquisite skills and expensive utensils are required, the price will be high. For example, if the ancient cast sword requires special iron, after thousands of trials, the price of the sword is extraordinary. Similarly, this 1% 2C3% 2C2-dioxacyclopentanone derivative, if the synthesis step is lengthy, the reagents used are precious, the cost will rise, and the price will follow.
Furthermore, look at its uses. If it is an indispensable raw material in important fields such as medicine and high-tech, such as the key ingredient of good medicine, or the necessity of advanced materials, the demand is strong and the supply is limited, and the price is not cheap. Just like the spices of ancient times, they are widely used in incense and medicine in rich and noble families, and the price is high and difficult to climb.
It is also necessary to check its market supply and demand. If there are many products, and there are few people who want them, the price may drop; if the demand is like a tide, and the production is insufficient, the price will rise. The ancient salt and iron, because it is related to people's livelihood, has constant demand. Although there is a fixed amount of production, it can also maintain the corresponding price.
Regional differences also have an impact. Different places have different prices due to traffic, taxation, and economic conditions. For example, ancient goods, in places with convenient transportation and prosperous economy, the price may be stable; in remote and isolated places, due to difficult transportation and increased costs, the price may be higher.
However, I do not know the current 1% 2C3% 2C2 -dioxetanone, 2- (3-bromo-5-chlorophenyl) -4% 2C4% 2C5% 2C5 -tetramethyl-specific conditions, it is difficult to determine the market price. Only by considering the above things comprehensively, it is possible to guess the approximate range of its price.