2 4 4 4 5 5 Tetramethyl 1 3 2 Dioxaborolan 2 Yl Phenyl 1h Imidazole
quinoline thiophene imidazole thiazole

2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-imidazole

    Specifications

    HS Code

    680403

    Chemical Formula C17H23BN2O2
    Molecular Weight 298.19
    Appearance Solid (usually)
    Solubility In Water Low (organic compound with non - polar groups)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, toluene
    Logp Positive (hydrophobic due to alkyl and aryl groups)

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    Frequently Asked Questions

    As a leading 2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-imidazole supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the chemical structure of 2- (4- (4,4,5,5-tetramethyl-1,3,2-dioxyboron heterocyclopentane-2-yl) phenyl) -1H-imidazole?
    The chemical structure of 2 - (4 - (4, 4, 5, 5 - tetramethyl - 1, 3, 2 - dioxaboronheterocyclopentane - 2 - yl)) phenyl - 1H - pyrazole. The structure of this compound is quite complex, so let me go through it in detail.
    First, its core structure is 1H - pyrazole, which is a five-membered heterocyclic ring containing two adjacent nitrogen atoms. The pyrazole ring is connected with a phenyl group, and the second position of the phenyl group is connected with a complex substituent. The substituent begins with 4- (4,4,5,5-tetramethyl-1,3,2-dioxaboronheterocyclopentane-2-yl). Among them, 4,4,5,5-tetramethyl-1,3,2-dioxaboronheterocyclopentane is a cyclic structure, the boron atom is connected to two oxygen atoms and two carbon atoms, and the 4 and 5 positions on the ring each have two methyl groups. The 2 position of this ring is connected to the 4 position of the above phenyl group. In this way, the chemical structure of 2- (4- (4,4,5,5-tetramethyl-1,3,2-dioxaboronheterocyclopentane-2-yl)) phenyl-1H-pyrazole is formed. Its unique structure may endow the compound with specific chemical and physical properties, and may have important uses in organic synthesis, drug development and other fields.
    What are the main uses of 2- (4- (4,4,5,5-tetramethyl-1,3,2-dioxoboropentane-2-yl) phenyl) -1H-imidazole?
    I look at what you said, the words are obscure, and it is difficult to understand their meaning. However, if you speculate in the classical style of "Tiangong Kaiwu", it may be explained in this way.
    The "2-%284-%284%2C4%2C5%2C5-%E5%9B%9B%E7%94%B2%E5%9F%BA-1%2C3%2C2-%E4%BA%8C%E6%B0%A7%E7%A1%BC%E6%9D%82%E7%8E%AF%E6%88%8A%E7%83%B7-2-%E5%9F%BA%29%E8%8B%AF%E5%9F%BA%29-1H-%E5%92%AA%E5%94%91" mentioned in this seems to be a complex chemical or process expression. Among them, "tetraethyl", "tellurium dioxide heterocycle", etc., are the names of chemical substances or structures.
    If its main use is studied, it may play an important role in the fields of chemicals and materials. "Tetraethyl" and the like can be used as additives to change the properties of compounds. For example, adding it to fuel oil can improve its combustion efficiency and anti-explosion performance. The "tellurium dioxide heterocyclic ring", because of its special ring structure, may have unique uses in organic synthesis, electronic materials, etc., or can participate in specific chemical reactions to prepare materials with special properties for the manufacture of electronic components, optical devices, etc.
    "1H-pyrazole" also has its uses. Pyrazole compounds are often important drug intermediates in the field of medicine, and can be used to synthesize antibacterial, anti-inflammatory, anti-tumor and other drugs. Due to their structural properties, they can interact with specific targets in organisms and exert pharmacological effects. In agriculture, they can be used as pesticide ingredients for insecticide and sterilization to protect crops. In materials science, it can be used to prepare functional materials, such as optoelectronic materials, etc., to endow materials with special optical and electrical properties.
    Although my solution may not be perfect, I hope to be able to follow the style of "Tiangong Kaiwu" to give you a little understanding of this meaning, so that you can know its use.
    What are the synthesis methods of 2- (4- (4,4,5,5-tetramethyl-1,3,2-dioxyboron heterocyclopentane-2-yl) phenyl) -1H-imidazole?
    To obtain the synthesis method of 2 - (4 - (4, 4, 5, 5 - tetraethyl - 1, 3, 2 - heterocyclopentaborane - 2 - yl dioxide)) benzyl - 1H - indole, can be considered from the following paths.
    First, it can be constructed by a step-by-step method. First, 4, 4, 5, 5 - tetraethyl - 1, 3, 2 - heterocyclopentaborane - 2 - yl related intermediates are prepared. The preparation of this intermediate may require a specific boron source and an alcohol containing a suitable substituent, catalyzed by a suitable catalyst such as Lewis acid, through a condensation reaction. After obtaining this intermediate, the coupling reaction is carried out with the indole derivative containing halogenated benzyl group. This coupling reaction may require the participation of transition metal catalysts such as palladium, such as Pd (PPh) as a catalyst, under basic conditions, such as potassium carbonate and other bases, when heated in a suitable organic solvent such as toluene, etc., to promote the formation of carbon-boron bonds, and then obtain the target product.
    Second, you can also try to use the indole parent as the starting material, and first benzylate the 2-position of the indole. The benzylation reagent can be selected from benzyl compounds containing appropriate leaving groups, such as benzyl halide. Under the action of alkali, such as strong bases such as sodium hydride, the indole 2-position carbon anion is formed, and then the benzyl halide undergoes nucleophilic substitution reaction, and benzyl is introduced. Then, 4, 4, 5-tetraethyl-1, 3, 2-heterocyclopentylborane-2-dioxide is introduced into the counterposition of benzyl. This introduction process can be achieved by the reaction of aryl halide and boron reagent, such as the use of boron reagents such as potassium tetraethylborate, under the catalysis of transition metals, through metallization-metallization-coupling and other steps to complete the modification, to obtain the target 2 - (4 - (4, 4, 5, 5 - tetraethyl - 1, 3, 2 - heterocyclopentylborane - 2 - yl)) benzyl - 1H - indole product.
    What are the physical properties of 2- (4- (4,4,5,5-tetramethyl-1,3,2-dioxyboron heterocyclopentane-2-yl) phenyl) -1H-imidazole?
    I look at what you said, this is a question related to chemical substances. However, its expression is complicated, and it seems to be some interpretation of the chemical formula. Now as far as I know, try to solve it for you.
    2- (4- (4,4,5,5-tetramethyl-1,3,2-dioxyboronheterocyclopentane-2-yl)) benzyl-1H-indole This substance has the following physical properties:
    In terms of appearance, it is mostly in solid form, due to intermolecular forces and structural arrangement. Its melting point varies according to the degree of purity and test conditions, but it is roughly in a specific temperature range. Due to the presence of aromatic rings and various groups in the molecule, the intermolecular forces have van der Waals forces, hydrogen bonds and other forms, which together affect the melting point.
    In terms of solubility, the substance has certain solubility in organic solvents such as dichloromethane and chloroform. Because its molecular structure contains hydrophobic benzyl and indole groups, it has similar compatibility with organic solvents. However, in water, due to the lack of sufficient hydrophilic groups, its solubility is poor.
    Its density is also an important physical property. Determined by molecular composition and spatial arrangement, the density is similar to that of the same type of aromatic ring and boron heterocyclic compounds.
    Furthermore, the stability of this substance is also key. The structure of intra-molecular boron heterocyclic and aromatic rings interacts, giving it a certain chemical stability. However, under extreme conditions such as strong acid, strong base, or high temperature and strong oxidant, the structure may change. Because the boron atoms in the boron heterocyclic ring have a certain electron deficiency, they are vulnerable to attack by nucleophiles, thus affecting the overall stability.
    In summary, 2 - (4 - (4, 4, 5, 5 - tetramethyl - 1, 3, 2 - dioxoborocyclopentane - 2 - yl)) benzyl - 1H - indole has a solid appearance, a specific melting point, a certain solubility in organic solvents, a specific density and chemical stability, all of which are due to its unique molecular structure.
    What is the market prospect of 2- (4- (4,4,5,5-tetramethyl-1,3,2-dioxoboropentane-2-yl) phenyl) -1H-imidazole?
    Today, there are 2- (4- (4,4,5,5-tetramethyl-1,3,2-dioxyboron-heterocyclopentane-2-yl) benzyl) -1H-pyrazole, and its market prospects are related to many parties.
    This compound may have potential in the field of pharmaceutical research and development. Due to its unique structure, it may be able to fit with specific biological targets, such as participating in the action pathways of some key enzymes, or affecting cell signaling pathways, it is expected to become a lead compound for new drugs. If the research and development goes well, in the treatment of specific diseases, or to create new methods, the market demand may be generated as a result, and the future is bright.
    In the field of materials science, it should not be underestimated. Its structural properties may endow the material with novel properties, such as being used as a special additive to improve the stability, optical or electrical properties of the material. If it can be successfully applied to emerging materials, with the vigorous development of the materials industry, its market demand will gradually increase, and the prospects are promising.
    However, there are also challenges. The process of synthesizing this compound may be complicated and expensive, limiting its large-scale production. And during marketing activities, it needs to cope with strict regulatory reviews and peer competition. If it can overcome synthesis problems, reduce costs, and pass regulatory reviews, it will stand out from the competition with high-quality performance, and its market prospects will be vast. It can occupy a place in both the pharmaceutical and materials markets and create considerable economic benefits.