1-% Jiang-3-methoxy-5- (trimethylsilyl) benzene, which has important uses in many fields.
In the field of medicinal chemistry, it can be used as a key intermediate to synthesize drug molecules with specific biological activities. Due to its unique chemical structure, it can give drugs specific properties, such as improving the lipid solubility of drug molecules, helping them to more easily penetrate biofilms and improve bioavailability. For example, when developing anti-cardiovascular drugs, by introducing this structure, it can enhance the affinity of drugs with specific targets and improve drug efficacy.
In the field of materials science, it can participate in the synthesis of high-performance organic materials. For example, the preparation of organic optoelectronic materials, using its structural properties to regulate the optoelectronic properties of materials, such as improving the material's luminous efficiency and stability. Applied to the manufacture of organic Light Emitting Diodes (OLEDs), it helps to improve the luminous quality and service life of display screens.
In the field of organic synthetic chemistry, as a building block for organic synthesis, it uses its silicon-based and methoxy-based reactivity to carry out diverse organic reactions, such as participating in the formation of carbon-carbon bonds and carbon-heteroatom bonds to construct complex organic molecular structures, providing an effective way for the synthesis of new organic compounds, enabling organic synthesis chemists to expand the compound library and explore new chemical substances and functions.
It can be seen that 1-% Jiang-3-methoxy-5- (trimethylsilyl) benzene plays a key role in many fields such as medicine, materials, and organic synthesis, promoting technological development and innovation in various fields.

1-%E6%B0%9F-3-%E7%94%B2%E6%B0%A7%E5%9F%BA-5-%28%E4%B8%89%E6%B0%9F%E7%94%B2%E5%9F%BA%29%E8%8B%AF, this substance is one of the organic compounds. Its physical properties are quite unique, let me talk about them one by one.
Looking at its state, under room temperature and pressure, it is mostly in a liquid state, with a relatively viscous texture, like a stagnant liquid, which flows slightly slowly. Compared with many common liquid substances, this state has unique flow characteristics.
As for the color, it usually shows a colorless and transparent shape, just like clear water, without any variegation, and pure and flawless.
Smell its smell, exuding a special fragrance, which is neither rich and pungent fragrance nor light and tasteless, but a unique fragrance, quite unique, once smelled, it is hard to forget.
When it comes to volatility, its volatility is weak. Left in the air for a long time, its mass loss is extremely slow, unlike some volatile substances, which disappear in an instant.
Another word density, compared to water, its density is slightly smaller. If it is placed in the same container as water, it can be seen floating lightly on the surface of the water, just like a light boat floating on the surface of a lake.
In terms of solubility, this substance is insoluble in water, and the two are like incompatible enemies and difficult to blend. However, it shows good solubility in organic solvents, such as ethanol, ether and other organic solvents, which can be fused with to form a uniform and stable solution.
The boiling point of this substance is quite high, and it needs to be applied to a higher temperature to make it boil into a gaseous state. As for the melting point, it is also relatively high. At room temperature, it can maintain a stable liquid state.
In summary, the 1-%E6%B0%9F-3-%E7%94%B2%E6%B0%A7%E5%9F%BA-5-%28%E4%B8%89%E6%B0%9F%E7%94%B2%E5%9F%BA%29%E8%8B%AF has unique physical properties such as liquid, colorless and transparent, special aromatic odor, weak volatility, less density than water, insoluble in water, high boiling point and high melting point.

The chemical properties of 1-% hydrocarbon-3-amino-5- (trihydrocarbyl) benzene are relatively stable. In this compound, the hydrocarbyl part has certain hydrophobicity and chemical inertness due to its hydrocarbon structure. Under common mild conditions, it is difficult to chemically react. It can dissolve well in many organic solvents, but it is difficult to dissolve in water, which is determined by the properties of the hydrocarbyl group itself. The functional group
3-amino gives the compound a certain alkalinity. The nitrogen atom in the amino group has a pair of lone pairs of electrons, which can be combined with protons, thus exhibiting alkaline characteristics. However, due to its surrounding chemical environment, this alkalinity is not extremely strong. In some specific acid-base reactions, amino groups can play a role in reacting with acids to form corresponding salts.
5 - (trihydrocarbon) benzene part, the benzene ring itself has a unique conjugated π electronic system, which endows the compound with certain stability. The conjugated structure of the benzene ring allows electrons to delocalize within the entire ring system, thereby reducing the energy of the molecule. This makes the benzene ring less susceptible to attack by nucleophiles under normal conditions. However, in the presence of specific catalysts and suitable reaction conditions, the benzene ring can undergo electrophilic substitution reactions, such as halogenation, nitrification, sulfonation and other reactions. The trihydrocarbon groups connected here will affect the electron cloud density distribution of the benzene ring, which in turn affects the activity and positional selectivity of the electrophilic substitution reaction on the benzene ring.
Overall, the parts of 1-% hydrocarbon-3-amino-5- (trihydrocarbyl) benzene interact with each other, and the overall chemical properties are relatively stable. However, under specific conditions and the action of suitable reagents, each part of the functional group can still exhibit corresponding chemical reactivity, participate in various organic synthesis reactions, and construct more complex organic compound structures.

To prepare 1-hydrocarbon-3-methoxy-5- (trihydrocarbon methyl) benzene, there are three methods.
First, benzene is used as the starting point. First, benzene and halogenated hydrocarbons are alkylated by Fu-g under the catalyst to obtain hydrocarbon benzene. Next, nitric acid and sulfuric acid are mixed to form a mixed acid to nitrate hydrocarbyl benzene to obtain nitrohydrocarbyl benzene. Then iron powder and hydrochloric acid are used to reduce the nitro group to amino group to obtain aminohydrocarbyl benzene. Then, methylation reagents such as dimethyl sulfate are used to convert the amino group into methoxy group to obtain 1-hydrocarbon-3-methoxybenzene. Finally, the target product 1-hydrocarbon-3-methoxybenzene was obtained by reacting the halogenated trihydrocarbon methane with 1-hydrocarbon-3-methoxybenzene under a suitable catalyst.
Second, phenol is used as the base. Phenol is first reacted with the halogenated hydrocarbon under basic conditions to introduce a hydrocarbon group to obtain hydrocarbyl phenol. Then dimethyl sulfate is used to methylate the phenol hydroxyl group to obtain 1-hydrocarbon-3-methoxybenzene. The next step is the same as the first method, that is, the reaction with the halogenated trihydrocarbon methane under the action of a catalyst to obtain 1-hydrocarbon-3-methoxy-5- (trihydrocarbon methyl) benzene.
Third, m-methoxybenzoic acid is used as the starting material. First, m-methoxybenzoic acid is reduced to m-methoxybenzyl alcohol, and reducing agents such as lithium aluminum hydride can be selected. M-methoxybenzyl alcohol is then reacted with a halogenating agent to obtain m-methoxyhalotoluene. After that, it is made into Grignard reagent, reacted with halogenated trihydrocarbon methane to form carbon-carbon bonds, and finally, after appropriate treatment, the protective groups that may be introduced are removed to obtain 1-hydrocarbon-3-methoxy-5 - (trihydrocarbon methyl) benzene. These three methods have their own advantages and disadvantages. The actual selection method depends on the trade-off of the availability of raw materials, the cost, the difficulty of reaction, and the yield.

What I am asking you is about the "price range of 1-Jiang-3-Methoxy-5- (trimethyl) silicon in the market". However, the matter is quite complicated, and the market price often changes due to many factors, making it difficult to determine the exact range.
First of all, the price of such substances is greatly affected by the cost of raw materials. The abundance of raw materials, the difficulty of mining, and the cost of obtaining them all determine their price. If raw materials are scarce or difficult to obtain, the cost will rise, and the price of this substance will also rise.
Second, the complexity of the production process is also critical. If production requires high-end technology and fine processes, involving special equipment and professionals, production costs will be high, and prices will rise.
Furthermore, the market supply and demand relationship has a significant impact. If demand is strong and supply is limited, merchants may raise prices to make a profit; if supply is abundant and demand is sluggish, prices will be under pressure to decline.
In addition, regional factors cannot be ignored. In different places, prices may vary due to differences in transportation costs and market competition. In places with convenient transportation and intense competition, prices may be relatively low; in remote areas and few supply channels, prices may be high.
Overall, in order to know the exact price range, it is necessary to pay attention to the market dynamics of chemical raw materials in real time, and consult relevant suppliers, distributors or industry experts to obtain more accurate information. However, in my opinion, it is difficult to say the specific price range at the moment, because the market is changing rapidly, and various factors are intertwined, resulting in price fluctuations.