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4-((2R)-2-(Chloromethyl)-3-Methylbutyl)-1-Methoxy-2-(3-Methoxypropoxy)Benzene
Linshang Chemical
|
HS Code |
765984 |
| Chemical Formula | C18H31ClO3 |
| Molecular Weight | 330.89 |
As an accredited 4-((2R)-2-(Chloromethyl)-3-Methylbutyl)-1-Methoxy-2-(3-Methoxypropoxy)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1 kg of 4-((2R)-2-(chloromethyl)-3 - methylbutyl)-1 - methoxy - 2-(3 - methoxypropoxy)benzene in sealed chemical drums. |
| Storage | Store 4-((2R)-2-(chloromethyl)-3 -methylbutyl)-1 -methoxy-2-(3 -methoxypropoxy)benzene in a cool, dry place, away from heat sources and direct sunlight. Keep it in a tightly - sealed container to prevent evaporation and contamination. It should be stored separately from incompatible substances, such as oxidizing agents and strong acids, in a well - ventilated area dedicated to chemical storage. |
| Shipping | Ship the chemical 4-((2R)-2-(chloromethyl)-3 - methylbutyl)-1 - methoxy - 2-(3 - methoxypropoxy)benzene in well - sealed, corrosion - resistant containers. Ensure compliance with hazardous chemical shipping regulations during transport. |
Competitive 4-((2R)-2-(Chloromethyl)-3-Methylbutyl)-1-Methoxy-2-(3-Methoxypropoxy)Benzene prices that fit your budget—flexible terms and customized quotes for every order.
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What is the main use of 4- ((2r) -2- (chloromethyl) -3-methylbutyl) -1-methoxy-2- (3-methoxypropoxy) benzene
4 - [ (2R) -2 - (chloromethyl) -3 -methylbutyl] -1 -methoxy-2 - (3 -methoxypropoxy) benzene, this compound is widely used in the field of chemical medicine.
In the process of pharmaceutical research and development, it may be a key intermediate. Through specific chemical reactions, specific functional groups can be added or transformed to construct novel compounds with unique pharmacological activities. When groups such as methoxy and propoxy in molecules give them specific physical and chemical properties, such as lipophilicity and stability, they can affect the absorption, distribution, metabolism and excretion of drugs when they interact with targets in organisms.
In the field of materials science, it may be involved in the creation of functional materials. Due to the complex combination of carbon chains and oxygen groups in its structure, it may endow materials with special electrical, optical or mechanical properties. For example, introducing it into polymer materials, or adjusting the solubility and film-forming properties of materials, makes materials emerge in electronic devices, optical coatings, etc.
Furthermore, in organic synthetic chemistry, as a characteristic structural unit, it can pave the way for the synthesis of complex natural products or functional molecules. Chemists can expand the complexity and diversity of molecular structures by manipulating their reactivity check points and carrying out various reactions, such as nucleophilic substitution, electrophilic addition, etc., providing rich raw materials and strategies for the creation of new compounds.
In the process of pharmaceutical research and development, it may be a key intermediate. Through specific chemical reactions, specific functional groups can be added or transformed to construct novel compounds with unique pharmacological activities. When groups such as methoxy and propoxy in molecules give them specific physical and chemical properties, such as lipophilicity and stability, they can affect the absorption, distribution, metabolism and excretion of drugs when they interact with targets in organisms.
In the field of materials science, it may be involved in the creation of functional materials. Due to the complex combination of carbon chains and oxygen groups in its structure, it may endow materials with special electrical, optical or mechanical properties. For example, introducing it into polymer materials, or adjusting the solubility and film-forming properties of materials, makes materials emerge in electronic devices, optical coatings, etc.
Furthermore, in organic synthetic chemistry, as a characteristic structural unit, it can pave the way for the synthesis of complex natural products or functional molecules. Chemists can expand the complexity and diversity of molecular structures by manipulating their reactivity check points and carrying out various reactions, such as nucleophilic substitution, electrophilic addition, etc., providing rich raw materials and strategies for the creation of new compounds.
What are the synthesis methods of 4- ((2r) -2- (chloromethyl) -3-methylbutyl) -1-methoxy-2- (3-methoxypropoxy) benzene
To prepare 4 - (2R) - 2 - (chloromethyl) - 3 - methylbutyl) - 1 - methoxy - 2 - (3 - methoxypropoxy) benzene, there are many methods, which can be selected according to the raw materials and conditions.
First, the benzene derivative with the corresponding substituent is used as the starting material. First, methoxy and 3 - methoxypropoxy are introduced into the phenyl ring, which can be obtained by nucleophilic substitution. If phenols are used as substrates, they can be reacted with halogenated methyl ether and 3 - halogenated propyl methyl ether under basic conditions to introduce the desired oxygen group.
Then, connect (2R) -2- (chloromethyl) -3 -methylbutyl at a specific position in the benzene ring. This step may require the participation of Grignard reagents, organolithium reagents, etc. If there is a halide containing (2R) -2- (chloromethyl) -3 -methylbutyl, it can react with metallized benzene derivatives to form a carbon-carbon bond, achieving the purpose of introducing the group. Attention should be paid to stereochemical control during the reaction to ensure the correct configuration of the product.
Or it can be thought in reverse, first construct a fragment containing (2R) -2- (chloromethyl) -3-methylbutyl, and then connect it with a benzene ring containing methoxy and 3-methoxypropoxy. This also requires selection to make the two effectively combine, and control the reaction conditions to ensure the selectivity and yield of the reaction.
Furthermore, the catalytic reaction can also be a good method. By using transition metal catalysis, such as palladium-catalyzed coupling reaction, each fragment can be precisely connected. Selecting aptamers and reaction conditions can promote the reaction to proceed efficiently and obtain the target product.
In conclusion, the method of synthesizing this compound must be based on the actual situation, considering the availability of raw materials, the difficulty of reaction, the cost, etc., and the optimal path must be selected to achieve the purpose of synthesis.
First, the benzene derivative with the corresponding substituent is used as the starting material. First, methoxy and 3 - methoxypropoxy are introduced into the phenyl ring, which can be obtained by nucleophilic substitution. If phenols are used as substrates, they can be reacted with halogenated methyl ether and 3 - halogenated propyl methyl ether under basic conditions to introduce the desired oxygen group.
Then, connect (2R) -2- (chloromethyl) -3 -methylbutyl at a specific position in the benzene ring. This step may require the participation of Grignard reagents, organolithium reagents, etc. If there is a halide containing (2R) -2- (chloromethyl) -3 -methylbutyl, it can react with metallized benzene derivatives to form a carbon-carbon bond, achieving the purpose of introducing the group. Attention should be paid to stereochemical control during the reaction to ensure the correct configuration of the product.
Or it can be thought in reverse, first construct a fragment containing (2R) -2- (chloromethyl) -3-methylbutyl, and then connect it with a benzene ring containing methoxy and 3-methoxypropoxy. This also requires selection to make the two effectively combine, and control the reaction conditions to ensure the selectivity and yield of the reaction.
Furthermore, the catalytic reaction can also be a good method. By using transition metal catalysis, such as palladium-catalyzed coupling reaction, each fragment can be precisely connected. Selecting aptamers and reaction conditions can promote the reaction to proceed efficiently and obtain the target product.
In conclusion, the method of synthesizing this compound must be based on the actual situation, considering the availability of raw materials, the difficulty of reaction, the cost, etc., and the optimal path must be selected to achieve the purpose of synthesis.
What are the physical properties of 4- ((2r) -2- (chloromethyl) -3-methylbutyl) -1-methoxy-2- (3-methoxypropoxy) benzene
This compound is named 4- [ (2R) -2 - (chloromethyl) -3 -methylbutyl] -1 -methoxy-2 - (3 -methoxypropoxy) benzene. Its physical properties are as follows:
This substance is mostly colorless to light yellow transparent liquid, pure and uniform in appearance, without obvious visible impurities. In terms of odor, it has a light special aromatic smell, is not pungent and unpleasant, and is relatively mild.
In terms of solubility, it exhibits good solubility in organic solvents such as ethanol, ether, chloroform, etc., and can be miscible with these solvents in any ratio. However, its solubility in water is extremely poor, almost insoluble, due to the large proportion of hydrophobic groups in its molecular structure, which makes it difficult to interact with polar solvents such as water.
When it comes to melting point and boiling point, due to the complexity of its structure, the melting point is relatively low, roughly in the range of -10 ° C to -5 ° C; the boiling point is higher, about 280 ° C to 290 ° C. The reason for the higher boiling point is that there are certain van der Waals forces and hydrogen bonds between molecules, which make it necessary to use more energy to overcome these forces during heating, thus gasifying.
In terms of density, it is slightly lighter than the density of water of 1g/cm ³, with a density of about 0.95-0.98g/cm ³, which means that when mixed with water, it will float in the upper layer of water.
The refractive index is an important indicator to measure its optical properties. The refractive index of this compound is relatively stable, about 1.48-1.50 at 20 ° C. This value has important reference value for the identification and analysis of this compound by optical means.
This substance is mostly colorless to light yellow transparent liquid, pure and uniform in appearance, without obvious visible impurities. In terms of odor, it has a light special aromatic smell, is not pungent and unpleasant, and is relatively mild.
In terms of solubility, it exhibits good solubility in organic solvents such as ethanol, ether, chloroform, etc., and can be miscible with these solvents in any ratio. However, its solubility in water is extremely poor, almost insoluble, due to the large proportion of hydrophobic groups in its molecular structure, which makes it difficult to interact with polar solvents such as water.
When it comes to melting point and boiling point, due to the complexity of its structure, the melting point is relatively low, roughly in the range of -10 ° C to -5 ° C; the boiling point is higher, about 280 ° C to 290 ° C. The reason for the higher boiling point is that there are certain van der Waals forces and hydrogen bonds between molecules, which make it necessary to use more energy to overcome these forces during heating, thus gasifying.
In terms of density, it is slightly lighter than the density of water of 1g/cm ³, with a density of about 0.95-0.98g/cm ³, which means that when mixed with water, it will float in the upper layer of water.
The refractive index is an important indicator to measure its optical properties. The refractive index of this compound is relatively stable, about 1.48-1.50 at 20 ° C. This value has important reference value for the identification and analysis of this compound by optical means.
What are the chemical properties of 4- ((2r) -2- (chloromethyl) -3-methylbutyl) -1-methoxy-2- (3-methoxypropoxy) benzene
This is an organic compound with complex chemical properties. From a structural perspective, the molecule contains benzene ring, chloromethyl, methoxy and alkoxy groups and other functional groups, each of which endows it with unique properties.
Let's talk about the benzene ring first. It is aromatic and quite stable, and can undergo electrophilic substitution reactions such as halogenation, nitration, and sulfonation. When the electrophilic reagent is close to the benzene ring, the large π bond electron cloud of the benzene ring attracts the electrophilic reagent, which in turn initiates the reaction. For example, under suitable conditions, with bromine in the catalyst, bromine atoms can replace hydrogen atoms on the benzene ring.
The chlorine atoms in chloromethyl groups are highly active and prone to nucleophilic substitution reactions. Due to its high electronegativity, the electron cloud in the carbon-chlorine bond is biased towards the chlorine atom, making the carbon atom partially positively charged and vulnerable to attack by nucleophiles. For example, when co-heated with sodium hydroxide aqueous solution, the chlorine atom can be replaced by hydroxyl groups to form alcohols.
Methoxy and alkoxy groups have electron induction and conjugation effects, which can increase the electron cloud density of the benzene ring, making the electrophilic substitution reaction on the benzene ring more likely to occur, and the reaction mainly occurs in the ortho and para-position.
From the perspective of physical properties, the compound should have a certain polarity due to its polar groups such as methoxy and alkoxy, and its solubility in organic solvents may be better than in water. However, the specific solubility is also related to the type of solvent and the interaction between molecules. In terms of boiling point, due to the interaction between van der Waals forces and polar groups between molecules, the boiling point may be relatively high.
In summary, this compound is chemically active and can participate in a variety of organic reactions. Its physical properties are also closely related to the functional groups in the structure, which is of great significance in organic synthesis and related fields.
Let's talk about the benzene ring first. It is aromatic and quite stable, and can undergo electrophilic substitution reactions such as halogenation, nitration, and sulfonation. When the electrophilic reagent is close to the benzene ring, the large π bond electron cloud of the benzene ring attracts the electrophilic reagent, which in turn initiates the reaction. For example, under suitable conditions, with bromine in the catalyst, bromine atoms can replace hydrogen atoms on the benzene ring.
The chlorine atoms in chloromethyl groups are highly active and prone to nucleophilic substitution reactions. Due to its high electronegativity, the electron cloud in the carbon-chlorine bond is biased towards the chlorine atom, making the carbon atom partially positively charged and vulnerable to attack by nucleophiles. For example, when co-heated with sodium hydroxide aqueous solution, the chlorine atom can be replaced by hydroxyl groups to form alcohols.
Methoxy and alkoxy groups have electron induction and conjugation effects, which can increase the electron cloud density of the benzene ring, making the electrophilic substitution reaction on the benzene ring more likely to occur, and the reaction mainly occurs in the ortho and para-position.
From the perspective of physical properties, the compound should have a certain polarity due to its polar groups such as methoxy and alkoxy, and its solubility in organic solvents may be better than in water. However, the specific solubility is also related to the type of solvent and the interaction between molecules. In terms of boiling point, due to the interaction between van der Waals forces and polar groups between molecules, the boiling point may be relatively high.
In summary, this compound is chemically active and can participate in a variety of organic reactions. Its physical properties are also closely related to the functional groups in the structure, which is of great significance in organic synthesis and related fields.
What is the market outlook for 4- ((2r) -2- (chloromethyl) -3-methylbutyl) -1-methoxy-2- (3-methoxypropoxy) benzene?
Today, there are compounds called 4- [ (2R) -2 - (chloromethyl) -3 -methylbutyl] -1 -methoxy-2 - (3 -methoxypropoxy) benzene. To understand its market prospects, it is like searching for treasures in the sea of commerce, and it is necessary to gain insights from many parties.
Looking at its field, if it is involved in pharmaceutical research and development, the pharmaceutical industry is booming today, and there is a strong demand for compounds with unique structures and activities. If this compound can exhibit specific pharmacological activities, such as antibacterial, anti-inflammatory or effective against specific disease targets, it will definitely find a place in the pharmaceutical market. However, the road to pharmaceutical research and development is full of obstacles, requiring rigorous clinical trials, time-consuming and huge investment. However, if successful, the rewards will be abundant.
In the field of materials science, if the compound can impart special properties to the material, such as improving the stability, solubility or optical properties of polymer materials, with the continuous innovation of materials science, the demand for novel compounds is increasing. It may emerge in high-end material manufacturing, and be applied to cutting-edge fields such as electronics and aerospace, with considerable market potential.
However, market competition should not be underestimated. Chemical synthesis technology is developing rapidly, or similar structural compounds have been developed or are being developed. To stand out in the market, efforts need to be made in cost control and production process optimization. An efficient and green synthesis process can not only reduce production costs, but also conform to the general trend of environmental protection and enhance product competitiveness.
Furthermore, policies and regulations are increasingly strict on chemical and related products. If the compound is used in commercial production, it needs to meet many regulatory requirements such as environmental protection and safety. Compliance operation is based on the foundation of the market, otherwise it will face penalties and market ban risks.
To sum up, the market prospect of 4- [ (2R) -2 - (chloromethyl) -3 - methylbutyl] -1 - methoxy - 2 - (3 - methoxypropoxy) benzene has both opportunities and challenges. By relying on its own characteristics to find precise application fields, optimize production processes and strictly abide by regulations, it has the opportunity to expand in the market and harvest success.
Looking at its field, if it is involved in pharmaceutical research and development, the pharmaceutical industry is booming today, and there is a strong demand for compounds with unique structures and activities. If this compound can exhibit specific pharmacological activities, such as antibacterial, anti-inflammatory or effective against specific disease targets, it will definitely find a place in the pharmaceutical market. However, the road to pharmaceutical research and development is full of obstacles, requiring rigorous clinical trials, time-consuming and huge investment. However, if successful, the rewards will be abundant.
In the field of materials science, if the compound can impart special properties to the material, such as improving the stability, solubility or optical properties of polymer materials, with the continuous innovation of materials science, the demand for novel compounds is increasing. It may emerge in high-end material manufacturing, and be applied to cutting-edge fields such as electronics and aerospace, with considerable market potential.
However, market competition should not be underestimated. Chemical synthesis technology is developing rapidly, or similar structural compounds have been developed or are being developed. To stand out in the market, efforts need to be made in cost control and production process optimization. An efficient and green synthesis process can not only reduce production costs, but also conform to the general trend of environmental protection and enhance product competitiveness.
Furthermore, policies and regulations are increasingly strict on chemical and related products. If the compound is used in commercial production, it needs to meet many regulatory requirements such as environmental protection and safety. Compliance operation is based on the foundation of the market, otherwise it will face penalties and market ban risks.
To sum up, the market prospect of 4- [ (2R) -2 - (chloromethyl) -3 - methylbutyl] -1 - methoxy - 2 - (3 - methoxypropoxy) benzene has both opportunities and challenges. By relying on its own characteristics to find precise application fields, optimize production processes and strictly abide by regulations, it has the opportunity to expand in the market and harvest success.
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