2-(3-Methoxypropoxy)-4-((R)-2-(Chloromethyl)-3-Methylbutyl)-1-Methoxybenzene
Linshang Chemical
HS Code |
723502 |
Chemical Formula | C18H29ClO3 |
Molecular Weight | 332.87 |
As an accredited 2-(3-Methoxypropoxy)-4-((R)-2-(Chloromethyl)-3-Methylbutyl)-1-Methoxybenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
Packing | 100 - gram bottle of 2-(3 - methoxypropoxy)-4-((R)-2-(chloromethyl)-3 - methylbutyl)-1 - methoxybenzene. |
Storage | Store 2-(3 - methoxypropoxy)-4-((R)-2-(chloromethyl)-3 - methylbutyl)-1 - methoxybenzene in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and oxidizing agents. Use air - tight containers, preferably made of corrosion - resistant materials like glass or certain plastics, to prevent leakage and contamination. |
Shipping | 2-(3 - methoxypropoxy)-4-((R)-2-(chloromethyl)-3 - methylbutyl)-1 - methoxybenzene is shipped in accordance with chemical transportation regulations. Packed securely in suitable containers, transported by approved carriers to ensure safe and proper delivery. |
Competitive 2-(3-Methoxypropoxy)-4-((R)-2-(Chloromethyl)-3-Methylbutyl)-1-Methoxybenzene prices that fit your budget—flexible terms and customized quotes for every order.
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"2- (3-methoxyethoxy) " indicates that there is a methoxyethoxy-containing substituent attached to the second carbon in the main chain. In this substituent, the methoxy group (-OCH
) is attached to the end of the ethoxy group (-OCH < CH < CH >), and the ethoxy group is connected to the main chain.
"4- ((R) -2 -chloroethyl) -3 -methylbutyl) ", with a complex substituent attached to the fourth carbon in the main chain. In this substituent, the third position of the butyl main chain has a methyl group, the second carbon is a chiral carbon, and the configuration is (R), and it is connected with chloroethyl. Chloroethyl is -CH ³ CH ³ Cl.
"1-methoxy naphthalene", revealing that the main structure is a naphthalene ring, and methoxy (-OCH 😉) is connected to the first carbon of the naphthalene ring.
In summary, this organic substance has a naphthalene ring as the core, with 1 methoxy group, 2 methoxy-ethoxy-containing substituents, and 4 chiral carbon and chloroethyl, methyl-containing butyl substituents. Its structure is complex, and each substituent affects each other, which plays an important role in the physical and chemical properties and reactivity of the organism. The existence of chiral carbon in the structure makes the organism have optical rotation, and the electronic and spatial effects of different substituents will also affect its stability, solubility, chemical reaction check point and activity.
The physical properties of 2 - (3 - methoxypropoxy) - 4 - ((R) - 2 - chloromethyl) - 3 - methylbutyl - 1 - methoxybenzene are very important and are related to many practical applications.
This compound is mostly in a liquid state at room temperature. Its boiling point is in a specific range, and the value of this boiling point is determined by factors such as intermolecular forces. Intermolecular forces include van der Waals forces, etc., so that it requires a specific energy to transform from liquid to gas, so the boiling point is a key physical property.
Furthermore, its melting point also has corresponding characteristics. The level of melting point reflects the degree of regularity of the internal structure of the crystal and the close bonding between molecules. If the internal structure is regular and the molecular bonding is close, the melting point is higher; otherwise, it is lower.
Solubility is also a physical property that cannot be ignored. In organic solvents, such as ethanol, ether, etc., its solubility is good, due to the principle of similar miscibility. The molecular structure of this compound is similar to that of organic solvents, so it can be well miscible. In water, its solubility is poor, because the polarity of water is quite different from the molecular polarity of the compound.
Density is also one of its physical properties. The value of its density characterizes the mass of the substance within a unit volume. Compared with other substances, this value can help to distinguish its floating or sinking conditions in the mixture, and is of great significance in operations such as separation and purification.
In addition, refractive index is also a physical property. Refractive index reflects the degree of refraction of light as it propagates in the compound, and is related to the molecular structure and concentration of the compound. It can be used in purity detection and other fields.
This substance is widely used in the field of organic synthesis. In medicinal chemistry, it is often regarded as a key intermediate. Due to its specific chemical structure and activity, it can participate in a variety of chemical reactions, helping to construct complex molecular structures with specific physiological activities, so as to promote the development of new drugs. For example, when developing drugs to treat specific diseases, the substance can introduce key functional groups through a series of reactions, thereby optimizing the activity and selectivity of drugs.
In the field of materials science, it can be used as an important starting material for the synthesis of materials with special properties. Through appropriate polymerization or reaction with other compounds, materials with unique physical and chemical properties can be prepared, such as materials with good thermal stability, mechanical properties or electrical properties, so as to meet the needs of high-performance materials in electronics, aerospace and other fields.
At the same time, in the field of organic catalysis, 2-%283-%E7%94%B2%E6%B0%A7%E5%9F%BA%E4%B8%99%E6%B0%A7%E5%9F%BA%29-4-%28%28R%29-2-%28%E6%B0%AF%E7%94%B2%E5%9F%BA%29-3-%E7%94%B2%E5%9F%BA%E4%B8%81%E5%9F%BA%29-1-%E7%94%B2%E6%B0%A7%E5%9F%BA%E8%8B%AF%E7%9A%84 can sometimes act as catalysts or catalyst ligands. By virtue of its structural properties, it can regulate the rate, selectivity and stereochemical results of the reaction, which is of great significance for the efficient and precise implementation of organic synthesis reactions.
First, benzene derivatives containing suitable substituents can be started. First, the benzene ring is connected to the methoxy group, and the halogenated methane can react with phenolic compounds under alkali catalysis to generate methoxybenzene. Then, try to introduce side chains. To obtain the 3-methoxyethoxy moiety, an ethoxy-containing and halogenated substance at one end, such as halogenated ethoxy methyl ether, can be selected and nucleophilized with the corresponding benzene derivative containing hydroxyl groups under appropriate conditions to form a 2- (3-methoxyethoxy) benzene intermediate.
As for the introduction of the 4- (R) -2-chloromethyl) -3-methylbutyl moiety, a halogen with a (R) -2-chloromethyl-3-methylbutyl structure can be prepared first, and then coupled with the above-mentioned intermediate with the participation of a metal catalyst such as a palladium catalyst.
Second, you can also start from the other side. First, the skeleton containing (R) -2-chloromethyl-3-methylbutyl is constructed, and the carbon chain structure is constructed by a series of nucleophilic substitutions and alkylations with appropriate halogenated hydrocarbons as starting materials. At the same time, a fragment containing 2- (3-methoxyethoxy) -1-methoxybenzene is prepared, and finally the two are connected. The reaction of Grignard reagent can be used to react with the prepared benzene derivative with (R) - 2-chloromethyl-3-methylbutyl halogen containing a halogen atom, or to use other carbon-carbon bond formation reactions such as the Ullman reaction, etc., to reach a connection, and the final product is 2 - (3-methoxyethoxy) - 4 - ((R) - 2-chloromethyl) - 3 - methylbutyl - 1 - methoxybenzene.
However, the method of synthesis requires careful consideration according to multiple factors such as the availability of raw materials, the difficulty of reaction conditions, and the requirements of yield and purity.
The first time is to observe its physical properties. This is an organic compound with specific chemical structures and properties. When operating, it is necessary to know its physical properties, such as melting point, boiling point, solubility, etc. Because it is related to storage and use conditions. If its physical properties are unknown, it is easy to cause improper storage, or the use of suitable solvents or reaction conditions cannot be selected according to its characteristics, resulting in experimental or production hindrance.
Safety is also a top priority. Organic compounds are often toxic, flammable or corrosive. It is necessary to thoroughly check their safety data to understand their potential harm to human health and the environment. Complete protective measures must be taken during operation, such as protective clothing, protective gloves and goggles. Work in a well-ventilated place to prevent the accumulation of harmful gases and endanger personal safety.
Furthermore, accurate measurement is indispensable. In chemical experiments and production, whether the dosage is accurate or not directly affects the reaction process and product quality. When weighing, use accurate instruments and operate according to specifications. If the dosage is wrong, the reaction may be incomplete, or the product may be impure, and even side reactions may be caused, which will affect the final result.
In addition, the control of reaction conditions should not be underestimated. Temperature, pressure, reaction time and other factors all have a great impact on the reaction. It is necessary to operate strictly according to the established reaction conditions. If the temperature is too high or too low, or the reaction time is too long or too short, the reaction may deviate from the expected direction and the ideal product cannot be obtained.
In terms of storage, an appropriate storage environment should be selected according to its physical properties. Store in a cool place away from light, away from fire sources and oxidants to prevent dangerous reactions. And it needs to be properly marked for easy access and management to prevent confusion and misuse.

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