2 5 Dibromo 3 Hexylthiophene
quinoline thiophene imidazole thiazole

2,5-dibromo-3-hexylthiophene

Taiy Chemical

    Specifications

    HS Code

    905352

    Chemical Formula C10H16Br2S
    Molecular Weight 326.01
    Appearance Solid (presumably, based on typical organosulfur - bromine compounds)
    Physical State At Room Temperature Solid
    Solubility In Organic Solvents Soluble in common organic solvents like chloroform, dichloromethane (推测基于其结构和相似化合物性质)
    Solubility In Water Insoluble (hydrophobic due to long alkyl chain and non - polar thiophene ring)
    Vapor Pressure Low (due to its solid state at room temperature)
    Stability Stable under normal conditions, but may react with strong oxidizing agents

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    Frequently Asked Questions

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    What is the chemical structure of 2,5-dibromo-3-hexylthiophene?
    The chemical structure of 2% 2C5-dibromo-3-hexylpentamide is involved in the field of organic chemistry. Its structure is formed by bonding specific atoms in a certain way.
    In this compound, pentamide is the basic structure, and pentamide is the structure formed by the reaction of the carboxyl group of pentanoic acid with ammonia or amine. The main chain of pentamide contains five carbon atoms, and its carbon chain is chain-like extension.
    At the 2nd and 5th positions of the main chain of pentamide, each connected to a bromine atom. Bromine atoms are highly electronegative and are covalently bonded to the main chain carbon atoms. This substitution causes the polarity of the molecule to change, which affects its physical and chemical properties.
    In addition, at the 3rd position of the main chain of pentamide, a monohexyl group is attached. Hexyl is an alkyl group containing six carbon atoms, which is connected to the main chain carbon atoms by a single bond. The introduction of hexyl increases the molecular carbon chain length and hydrophobicity.
    Thus, the chemical structure of 2% 2C5-dibromo-3-hexylpentamide is composed of the main chain of pentamide, the bromine atoms at the 2nd and 5th positions, and the hexyl group at the 3rd position. The interaction of each part jointly determines the unique properties and reactivity of the compound, and may have specific uses and significance in the fields of organic synthesis, medicinal chemistry, etc.
    What are the main uses of 2,5-dibromo-3-hexylthiophene?
    2% 2C5-dibromo-3-hexylthiophene, this substance is widely used in various fields of chemical industry.
    In the field of organic synthesis, it is a key intermediate. With its unique structure, it can be derived from many chemical reactions. If it is coupled, it can be connected with other halogenated hydrocarbon-containing substances to build complex macromolecules, paving the way for the creation of new materials and pharmaceutical active ingredients.
    In the field of materials science, it also plays a pivotal role. It is often used in the preparation of conductive polymer materials. Adding this substance can optimize the conductivity of polymers, and is frequently used in the preparation of organic semiconductors and conductive films. Such conductive materials play a key role in devices such as organic Light Emitting Diodes (OLEDs) and organic field effect transistors (OFETs), which can improve the photoelectric properties of devices, such as enhancing luminous efficiency and improving carrier mobility.
    Furthermore, in the field of medicinal chemistry, its potential value should not be underestimated. Although not directly developed into drugs, as intermediates, they can be structurally modified and modified, or compounds with specific biological activities can be obtained, providing possible directions for the development of new drugs.
    In summary, 2% 2C5-dibromo-3-hexylthiophene has important uses in organic synthesis, materials science, medicinal chemistry, and other fields, and plays a significant role in promoting the development of related fields.
    What are the synthesis methods of 2,5-dibromo-3-hexylthiophene?
    The synthesis method of 2% 2C5-dibromo-3-hexylpentamide is often involved in the synthesis of organic chemistry. One of these methods is based on pentamide, and bromine atoms are added to a specific check point by bromination reaction.
    First take an appropriate amount of pentamide and dissolve it into a suitable organic solvent, such as dichloromethane or tetrahydrofuran, which can well dissolve the reactants and have stable chemical properties and do not disturb the reaction process. Stir well to create a homogeneous environment for efficient reaction.
    Then, under low temperature and temperature control conditions, slowly add bromine sources. The commonly used bromine sources include bromine elemental substance or N-bromosuccinimide (NBS). Taking NBS as an example, the reaction is mild and easy to control, which can reduce the probability of side reactions. Under low temperature conditions, such as about 0 ° C, the bromination check point can be precisely controlled, and bromine atoms are mainly introduced at the 2,5 position.
    After the bromination step is completed, the reaction system may contain unreacted raw materials, by-products, etc. It needs to be separated and purified to obtain a pure target product. First, wash with water to remove impurities that are easily soluble in water. Then extract with an organic solvent to collect the organic phase. Following column chromatography, the suitable silica gel column and eluent were selected to separate and obtain pure 2,5-dibromo-3-hexylvaleramide by the difference in the partition coefficients of each component in the stationary phase and the mobile phase.
    Another way is to start from hexylvaleric acid and first convert it into the corresponding acid chloride, commonly used chlorination reagents such as dichlorosulfoxide. The acid chloride has high activity and is easier to react with ammonia or amines to form amides. After the amide is formed, the bromination step can also be performed to obtain the target product. In this process, the reaction conditions at each step need to be precisely regulated to obtain 2% 2C5-dibromo-3-hexylpentamide with high purity and high yield.
    What are the physical properties of 2,5-dibromo-3-hexylthiophene?
    2% 2C5-dibromo-3-methylpentamide is an organic compound, and its physical properties are as follows:
    Viewed at room temperature, it is mostly in the state of white crystalline powder, which is common in many organic solid compounds and is conducive to storage and handling. Its powder has a fine texture and a relatively uniform particle size distribution, which is crucial for its dispersion and reactivity in chemical reactions and industrial production.
    Smell, this compound has a weak special smell. However, the smell is not pungent and unpleasant, but relatively mild. However, during operation and use, it is still necessary to pay attention to ventilation to prevent odor accumulation and discomfort.
    When it comes to melting point, the melting point of 2% 2C5-dibromo-3-methylpentamide is about [specific value]. As an important physical property of the substance, the melting point is of great significance for its identification, purity judgment and processing applications. At this melting point temperature, the compound changes from solid state to liquid state, and this phase change process is widely used in material processing, purification and other fields.
    In terms of solubility, it is insoluble in water, but soluble in some organic solvents, such as ethanol and acetone. This difference in solubility is based on the principle of similarity and miscibility. Due to its molecular structure characteristics, the force between it and organic solvent molecules is stronger, so it can be better dissolved in it. This property is widely used in organic synthesis, separation and purification processes, and can be separated and purified by the difference in solubility of different solvents.
    What is the price range of 2,5-dibromo-3-hexylthiophene in the market?
    The price range of 2% 2C5-dibromo-3-methylvaleramide in the market is difficult to say exactly. The price depends on various factors, such as the source and flow of materials, the difficulty of preparation, the amount of market demand, and the situation of competition in the same industry.
    If the material is widely sourced and easy to obtain, the preparation process is simple and efficient, and the market demand is stable and there is no fierce competition, the price may tend to be easy. On the contrary, if the material is rare, the preparation is complicated, the market demand is strong and the supply is tight, and the competition in the same industry promotes its value-added, the price will be high.
    Looking at the past market conditions, its price often fluctuates. From time to time, due to sudden shortages of raw materials or process improvements, prices have risen and fallen sharply. Therefore, in order to know the exact price range, it is necessary to pay close attention to the dynamics of the chemical raw material market, carefully examine the quotations of various suppliers, and obtain a more accurate price according to specific quality, quantity and other factors. Or you can consult the chemical product trading platform, industry brokers, or directly inquire with the manufacturer, and it is expected to be close to the current market price range.