2 Hydroxythiophene
Quinoline Thiophene Imidazole Thiazole
2-Hydroxythiophene
Chemical Formula C4H4OS
Molar Mass 100.14 g/mol
Appearance Solid
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents
FAQ

What are the main uses of 2-Hydroxythiophene?

2-Hydroxythiophene is also an organic compound. It has a wide range of uses and has important applications in many fields.

Bearing the brunt, in the field of medicinal chemistry, 2-Hydroxythiophene is a key synthetic building block. With it as a base, chemists can construct drug molecules with diverse structures. Due to its unique structure, the cover can endow the synthesized drug with specific biological activities, such as antibacterial, anti-inflammatory, and anti-tumor effects. For example, through ingenious chemical reactions, linking 2-Hydroxythiophene with other active groups can develop new antibacterial drugs to deal with the increasingly serious problem of bacterial drug resistance.

Furthermore, in the field of materials science, 2-hydroxythiophene also shines. Because of its conjugated structure, it shows great potential in the field of optoelectronic materials. It can be used to prepare organic Light Emitting Diode (OLED) materials. With its good luminous properties, it can improve the luminous efficiency and color purity of OLEDs, so that the color gamut of the display screen is wider and the image quality is clearer. In addition, in the research and development of solar cell materials, 2-hydroxythiophene can also play a role, which helps to improve the photoelectric conversion efficiency of solar cells and promote the development of renewable energy.

In organic synthesis chemistry, 2-hydroxythiophene, as a reaction substrate, participates in many organic reactions. The unique activity of its hydroxyl group and thiophene ring can initiate various reactions such as nucleophilic substitution and electrophilic substitution, providing a convenient way for the synthesis of complex organic compounds. With this, chemists can construct organic molecules with special structures and functions to meet the needs of specific organic compounds in different fields.

In summary, 2-hydroxythiophene plays an indispensable role in the fields of medicine, materials, and organic synthesis, and is of great significance for promoting scientific research and technological development in various fields.

What are the physical properties of 2-Hydroxythiophene?

2-Hydroxythiophene is one of the organic compounds. Its physical properties are quite important and are listed as follows:
First appearance and properties, at room temperature, 2-Hydroxythiophene is often white to light yellow crystalline powder, with fine texture. It can be seen by the eye and can be felt by hand. This appearance characteristic is quite critical in the identification and preliminary cognition of the substance. It can be obtained by naked eye observation.
Second and melting point, the melting point of 2-Hydroxythiophene is about a specific temperature range. For the melting point, the critical temperature at which a substance changes from a solid state to a liquid state. This characteristic is crucial for defining its physical state at different temperatures. Accurately knowing the melting point helps to control the temperature conditions in experiments and industrial production to ensure that the substance is in the desired state, and can also provide an important basis for purity testing. The melting point often changes due to the presence of impurities.
In addition, solubility, 2-hydroxythiophene exhibits different solubility in a variety of organic solvents. In common organic solvents such as ethanol, ether, etc., it has a certain solubility. This solubility characteristic makes it possible to select a suitable solvent according to its solubility in the process of chemical reaction, separation and purification or preparation to achieve the desired chemical operation. For example, in the synthesis reaction, the selection of a suitable solvent can promote the full contact of the reactants and improve the reaction efficiency; in the separation process, the difference in solubility can be used to effectively separate 2-hydroxythiophene from the mixture.
Also on the density, although its density value is not as widely known as some common substances, in specific chemical production and scientific research scenarios, density data are indispensable. Density reflects the mass per unit volume of a substance. For processes involving volume and mass conversion, such as material measurement, reactor loading calculation, etc., accurate density data is a key factor to ensure the accuracy of production and experiments.
In addition, 2-hydroxythiophene may have a certain odor. Although odor is not its most critical physical property, it can be used as an intuitive basis for judgment during actual operation and use. A specific odor may indicate the presence or absence of the substance. At the same time, it also has certain significance for the safety and comfort of the operating environment. If the odor is pungent or has a special odor, corresponding protective measures need to be taken to protect the health of the operator.

In summary, the physical properties of 2-hydroxythiophene, such as appearance, melting point, solubility, density and odor, are of great significance in chemical research, industrial production and related application fields. In-depth understanding and mastering of these properties can make better use of this compound.

Is 2-Hydroxythiophene chemically stable?

The stability of the chemical properties of 2-hydroxythiophene depends on many aspects.

This compound contains hydroxyl groups and thiophene rings. Hydroxyl groups are active and can participate in many reactions. Because the oxygen atom has lone pairs of electrons, it is easy to bind to protons, showing a certain acidity and can neutralize with bases. And the hydroxyl groups can be esterified to form ester compounds with acids.

thiophene rings are aromatic systems and have certain stability. However, the electron cloud density distribution of the thiophene ring is uneven, and the electron cloud density of the α-position is relatively high, which is more prone to electrophilic substitution. Therefore, in the electrophilic substitution reaction of 2-hydroxythiophene, the localization effect of the hydroxyl group interacts with the activity of the thiophene ring itself.

In terms of stability, the presence of the hydroxyl group may affect the electron cloud distribution of the thiophene ring, causing its stability to change slightly. In the air, the hydroxyl group may be oxidized, which affects its stability. However, under appropriate conditions, if unfavorable factors such as oxidation can be avoided, 2-hydroxythiophene can also maintain a relatively stable state. In specific organic solvents, its solubility may play a role in stability. If the solvent interacts with 2-hydroxythiophene, such as hydrogen bonds, it may increase its stability; conversely, if the solvent promotes its chemical reaction, the stability will decrease. Therefore, the chemical stability of 2-hydroxythiophene depends on the specific environment and conditions, and cannot be generalized.

What are the synthesis methods of 2-Hydroxythiophene?

The synthesis method of 2-hydroxythiophene is an important research direction in the field of chemistry. The ancient chemical synthesis followed the classical path and went through several steps to achieve the goal.

One method can be started from thiophene derivatives. First, thiophene is halogenated at a specific position with a suitable halogenating reagent to obtain halogenated thiophene. For example, bromine is introduced into the thiophene ring with the assistance of a catalyst. Then, the halogenated thiophene is reacted with a nucleophile, which contains hydroxyl-related groups. After nucleophilic substitution, the halogen atom is replaced by a hydroxyl group, and then 2-hydroxythiophene is obtained. This process requires fine regulation of reaction conditions, such as temperature, solvent, and reactant ratio. If the temperature is too high or too low, it can cause a cluster of side reactions and affect the yield.

The second method can be synthesized by cyclization reaction from simple compounds containing sulfur and hydroxyl groups. If a specific thioenol-containing compound is used, under suitable catalyst and reaction conditions, cyclization occurs in the molecule to construct a thiophene ring, while retaining the hydroxyl group in the 2 position. This cyclization reaction requires a high degree of catalyst, and the type and amount of catalyst need to be precisely selected to promote the efficient and directional progress of the reaction.

In addition, there are also methods of metal catalysis. Using the unique activity and selectivity of metal catalysts, the substrate molecules are activated to guide the reaction in the direction of generating 2-hydroxythiophene. Metal catalysts can often reduce the activation energy of the reaction and accelerate the reaction process. However, the recovery and reuse of metal catalysts are also key factors to be considered in practical applications.

All these synthesis methods have their own advantages and disadvantages. In practical application, the ideal synthesis effect can be achieved when considering various factors such as raw material availability, cost, reaction conditions and product purity, and making careful choices.

What is the price range of 2-Hydroxythiophene in the market?

Today, I am inquiring about the price of 2 - Hydroxythiophene in the market. This product is also a chemical product. However, the price between the markets is wide and narrow, and it is difficult to be sure. The price varies according to the quality, the amount of sources, and the urgency of the demand.

If it is common sense, the price of chemical reagents varies depending on the specification. High purity, the price must be high; ordinary products are slightly cheaper. And different suppliers have different pricing.

Look at the market of various chemical materials, the price of similar products may vary by twice. To get a definite price, ask a merchant specializing in chemical reagents. It can tell the nearest price according to the current market conditions and the status of the goods.

Or on the trading platform of chemical raw materials, check the records of its price in detail, and you can also get an approximate range. However, the prices of these platforms are not constant and change with the market. In short, if you want to know the price of 2-Hydroxythiophene, you must consult the merchants and observe the platforms to measure the situation of the market.