Linshang Chemical
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1-(Chloromethyl)-3,5-Dinitrobenzene
Linshang Chemical
|
HS Code |
676628 |
| Chemical Formula | C7H3ClN2O4 |
| Molar Mass | 216.56 g/mol |
| Appearance | Yellow solid |
| Odor | Pungent |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in common organic solvents like benzene, toluene |
| Melting Point | 90 - 92 °C |
| Boiling Point | Decomposes before boiling |
| Density | 1.66 g/cm³ |
| Hazard Class | Toxic, corrosive |
As an accredited 1-(Chloromethyl)-3,5-Dinitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 1-(chloromethyl)-3,5 - dinitrobenzene in sealed, labeled chemical - grade container. |
| Storage | 1-(Chloromethyl)-3,5 -dinitrobenzene should be stored in a cool, dry, well - ventilated area, away from heat sources and open flames. It must be kept in a tightly sealed container to prevent leakage. Store it separately from oxidizing agents, reducing agents, and other incompatible substances to avoid potential chemical reactions. |
| Shipping | 1-(Chloromethyl)-3,5 -dinitrobenzene is a hazardous chemical. Shipping requires proper packaging in accordance with regulations, labeled clearly. It must be transported by carriers approved for handling such chemicals with safety precautions. |
Competitive 1-(Chloromethyl)-3,5-Dinitrobenzene prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615365006308 or mail to info@alchemist-chem.com.
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Tel: +8615365006308
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As a leading 1-(Chloromethyl)-3,5-Dinitrobenzene supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
What are the physical properties of 1- (chloromethyl) -3,5-dinitrobenzene?
1 - (methoxy) -3,5 - di-tert-butylbenzene, this substance has many physical properties. At room temperature, it is mostly colorless to light yellow transparent liquid, and its properties are stable. Looking at its color, pure ones are light in color, and impurities can cause slight color changes.
When it comes to odor, it often emits a weak and special aromatic smell, which is not pungent and unpleasant, but can be sensed by those with a keen sense of smell. The boiling point value fluctuates slightly due to environmental pressure, about a specific temperature range. This temperature makes it change from liquid to gaseous state, reflecting the strength of intermolecular forces.
The density is moderate, which is different from common organic solvents, causing it to be stratified according to the density in the mixed system. Good solubility, can be miscible with most organic solvents such as ethanol, ether, toluene, etc. Due to the principle of similar phase dissolution, the molecular structure is similar to each other so that it is easy to mix evenly, but it is difficult to dissolve in water, because its molecular polarity is different from water.
In addition, the melting point of 1- (methoxy) -3,5 -di-tert-butylbenzene is also a key physical property. At a specific temperature, solid and liquid states are transformed into each other, and this temperature is determined by molecular arrangement and interaction. Overall, these physical properties lay the foundation for their application in chemical, materials and other fields, providing important reference for related research and production.
When it comes to odor, it often emits a weak and special aromatic smell, which is not pungent and unpleasant, but can be sensed by those with a keen sense of smell. The boiling point value fluctuates slightly due to environmental pressure, about a specific temperature range. This temperature makes it change from liquid to gaseous state, reflecting the strength of intermolecular forces.
The density is moderate, which is different from common organic solvents, causing it to be stratified according to the density in the mixed system. Good solubility, can be miscible with most organic solvents such as ethanol, ether, toluene, etc. Due to the principle of similar phase dissolution, the molecular structure is similar to each other so that it is easy to mix evenly, but it is difficult to dissolve in water, because its molecular polarity is different from water.
In addition, the melting point of 1- (methoxy) -3,5 -di-tert-butylbenzene is also a key physical property. At a specific temperature, solid and liquid states are transformed into each other, and this temperature is determined by molecular arrangement and interaction. Overall, these physical properties lay the foundation for their application in chemical, materials and other fields, providing important reference for related research and production.
What are the chemical properties of 1- (chloromethyl) -3,5-dinitrobenzene?
1 - (methoxy) -3,5 -dimethylphenol, this is an organic compound. Its chemical properties are quite rich, let me explain in detail for you.
First, the phenolic hydroxyl group endows it with acidity. Due to the strong electronegativity of the oxygen atoms in the phenolic hydroxyl group, the polarity of the hydrogen-oxygen bond increases, and the hydrogen atoms are more likely to leave in the form of protons, thus showing a certain acidity, which can react with bases to generate corresponding phenolic salts.
Furthermore, it has electrophilic substitution reaction activity. The phenolic hydroxyl group is an adjacent and para-site locator, which can increase the electron cloud density of the phenyl ring and make it more susceptible to attack by electrophilic reagents. In the adjacent and para-site of the phenyl ring, electrophilic substitution reactions such as halogenation, nitrification, and sulfonation are For example, when it encounters bromine water, it will rapidly undergo bromination reaction at the ortho and para-sites of phenolic hydroxyl groups to form white precipitates, which is often used to test phenolic compounds.
In addition, the methoxy group in this compound, as the donator group, also affects the electron cloud distribution of the benzene ring, enhances the electron cloud density of the benzene ring, and further enhances the electrophilic substitution reaction activity. At the same time, the steric resistance effect of the methoxy group may play a role in the selectivity of the reaction.
And methyl is also the donator group, which increases the electron cloud density of the benzene ring and promotes the electrophilic substitution reaction. However, the donator capacity of methyl is slightly different from that of methoxy group, and the two work together to make the reactivity and selectivity of this compound unique.
1- (methoxy) -3,5-dimethylphenol has unique chemical properties and may have important applications and research values in organic synthesis, medicinal chemistry and other fields.
First, the phenolic hydroxyl group endows it with acidity. Due to the strong electronegativity of the oxygen atoms in the phenolic hydroxyl group, the polarity of the hydrogen-oxygen bond increases, and the hydrogen atoms are more likely to leave in the form of protons, thus showing a certain acidity, which can react with bases to generate corresponding phenolic salts.
Furthermore, it has electrophilic substitution reaction activity. The phenolic hydroxyl group is an adjacent and para-site locator, which can increase the electron cloud density of the phenyl ring and make it more susceptible to attack by electrophilic reagents. In the adjacent and para-site of the phenyl ring, electrophilic substitution reactions such as halogenation, nitrification, and sulfonation are For example, when it encounters bromine water, it will rapidly undergo bromination reaction at the ortho and para-sites of phenolic hydroxyl groups to form white precipitates, which is often used to test phenolic compounds.
In addition, the methoxy group in this compound, as the donator group, also affects the electron cloud distribution of the benzene ring, enhances the electron cloud density of the benzene ring, and further enhances the electrophilic substitution reaction activity. At the same time, the steric resistance effect of the methoxy group may play a role in the selectivity of the reaction.
And methyl is also the donator group, which increases the electron cloud density of the benzene ring and promotes the electrophilic substitution reaction. However, the donator capacity of methyl is slightly different from that of methoxy group, and the two work together to make the reactivity and selectivity of this compound unique.
1- (methoxy) -3,5-dimethylphenol has unique chemical properties and may have important applications and research values in organic synthesis, medicinal chemistry and other fields.
What are the main uses of 1- (chloromethyl) -3,5-dinitrobenzene?
The main use of 1 - (cyanomethyl) -3,5 -dihydroxybenzene is described in "Tiangong Materials", which is related to general engineering and practical applications.
In terms of engineering, it may be used in certain dyes. Due to its specific chemical and general chemical properties, it can produce color and good quality dyes, which can be used for printing and dyeing of materials. Ancient dyes are prosperous, this compound can help craftsmen obtain colorful materials, and the clothes of the rich.
In the field of application, 1 - (cyanomethyl) -3,5 -dihydroxybenzene may have certain chemical activity. Or it can be used in the synthesis of some middle herbs, or it has the functions of clearing and detoxifying, promoting blood circulation and removing blood stasis. In ancient times, the source of natural compounds has been explored for many years to identify the practical value of many substances. This compound may be processed, compatible and other means, and it may also have its presence in the ancient incense industry. Because of its chemical properties, or it can be combined with fragrances, it makes the incense more mellow and long-lasting, adding elegance to the lives of the ancients.
Therefore, 1- (cyanomethyl) -3,5-dihydroxybenzene may play an important role in engineering, application and other aspects, reflecting the wisdom of ancient technology and technology.
In terms of engineering, it may be used in certain dyes. Due to its specific chemical and general chemical properties, it can produce color and good quality dyes, which can be used for printing and dyeing of materials. Ancient dyes are prosperous, this compound can help craftsmen obtain colorful materials, and the clothes of the rich.
In the field of application, 1 - (cyanomethyl) -3,5 -dihydroxybenzene may have certain chemical activity. Or it can be used in the synthesis of some middle herbs, or it has the functions of clearing and detoxifying, promoting blood circulation and removing blood stasis. In ancient times, the source of natural compounds has been explored for many years to identify the practical value of many substances. This compound may be processed, compatible and other means, and it may also have its presence in the ancient incense industry. Because of its chemical properties, or it can be combined with fragrances, it makes the incense more mellow and long-lasting, adding elegance to the lives of the ancients.
Therefore, 1- (cyanomethyl) -3,5-dihydroxybenzene may play an important role in engineering, application and other aspects, reflecting the wisdom of ancient technology and technology.
What are the synthesis methods of 1- (chloromethyl) -3,5-dinitrobenzene?
To prepare 1 - (cyanomethyl) -3,5 -dihydroxybenzene, there are various ways to synthesize it, which are described in detail below.
First, it can be started by a suitable phenolic compound. First, the phenols are substituted with cyanogen-containing reagents under specific conditions. For example, the reaction of phenol with halogenated acetonitrile is catalyzed by a base. The base can remove the hydrogen of the phenolic hydroxyl group to form a phenoxy negative ion. This negative ion has strong nucleophilicity and can attack the carbon connected to the halogen atom of halogenated acetonitrile, and the halogen atom leaves, thereby introducing the cyanogen methyl group. Subsequently, the resulting product is hydroxylated. A suitable oxidizing agent or hydroxylating agent can be used to introduce hydroxyl groups at specific positions in the benzene ring to achieve the target structure of 3,5-dihydroxyl groups. This process requires fine regulation of reaction conditions, such as temperature, reaction time, and reagent dosage. Due to the high activity of phenolic compounds, improper conditions are prone to overreaction.
Second, it is also possible to start from compounds containing benzene rings with functional groups that can be converted into cyanomethyl and hydroxyl groups. For example, first use compounds with suitable substituents, such as ester groups, attached to the benzene ring as raw materials. Through the hydrolysis of ester groups, the corresponding carboxylic acid can be obtained. After that, the carboxylic acid is converted into a halogen, and then reacted with a cyanide reagent to introduce a cyanide group, and then the cyanide group is converted into a cyanide methyl group through hydrolysis and reduction. As for the introduction of hydroxyl groups, according to the positioning effect of the existing substituents on the benzene ring, the appropriate electrophilic substitution reaction conditions can be selected to introduce the hydroxyl group to the 3,5-position.
Third, some special organic synthesis strategies can also be considered. For example, using a metal-catalyzed coupling reaction. First prepare compounds containing benzene rings and groups such as suitable halogen atoms or borate esters, and at the same time prepare reagents containing cyanide methyl groups and groups that can be coupled with the former. Under the action of metal catalysts, such as palladium catalysts, a coupling reaction occurs to form a carbon-carbon bond, and cyanogen methyl is introduced. After that, the benzene ring is hydroxylated. This method requires higher reaction conditions and catalysts, but it can construct the target molecular structure more accurately.
First, it can be started by a suitable phenolic compound. First, the phenols are substituted with cyanogen-containing reagents under specific conditions. For example, the reaction of phenol with halogenated acetonitrile is catalyzed by a base. The base can remove the hydrogen of the phenolic hydroxyl group to form a phenoxy negative ion. This negative ion has strong nucleophilicity and can attack the carbon connected to the halogen atom of halogenated acetonitrile, and the halogen atom leaves, thereby introducing the cyanogen methyl group. Subsequently, the resulting product is hydroxylated. A suitable oxidizing agent or hydroxylating agent can be used to introduce hydroxyl groups at specific positions in the benzene ring to achieve the target structure of 3,5-dihydroxyl groups. This process requires fine regulation of reaction conditions, such as temperature, reaction time, and reagent dosage. Due to the high activity of phenolic compounds, improper conditions are prone to overreaction.
Second, it is also possible to start from compounds containing benzene rings with functional groups that can be converted into cyanomethyl and hydroxyl groups. For example, first use compounds with suitable substituents, such as ester groups, attached to the benzene ring as raw materials. Through the hydrolysis of ester groups, the corresponding carboxylic acid can be obtained. After that, the carboxylic acid is converted into a halogen, and then reacted with a cyanide reagent to introduce a cyanide group, and then the cyanide group is converted into a cyanide methyl group through hydrolysis and reduction. As for the introduction of hydroxyl groups, according to the positioning effect of the existing substituents on the benzene ring, the appropriate electrophilic substitution reaction conditions can be selected to introduce the hydroxyl group to the 3,5-position.
Third, some special organic synthesis strategies can also be considered. For example, using a metal-catalyzed coupling reaction. First prepare compounds containing benzene rings and groups such as suitable halogen atoms or borate esters, and at the same time prepare reagents containing cyanide methyl groups and groups that can be coupled with the former. Under the action of metal catalysts, such as palladium catalysts, a coupling reaction occurs to form a carbon-carbon bond, and cyanogen methyl is introduced. After that, the benzene ring is hydroxylated. This method requires higher reaction conditions and catalysts, but it can construct the target molecular structure more accurately.
What are the precautions for 1- (chloromethyl) -3,5-dinitrobenzene during storage and transportation?
1 - (methoxy) -3,5 -dicarboxylbenzene should pay attention to the following matters during storage and transportation:
First, because of its chemical properties, the storage environment requirements are quite high. It should be placed in a cool, dry and well-ventilated place, and must not be close to fire or heat sources. Because if the substance is heated, it may cause chemical reactions, cause it to deteriorate or pose a safety risk. For example, high temperature may cause reactions such as dehydration of functional groups such as carboxyl groups, affecting their chemical structure and properties.
Second, when storing, it must be stored separately from oxidants and reducing agents, and must not be mixed. The carboxyl group in Gein 1- (methoxy) -3,5-dicarboxylbenzene has a certain acidity, and the methoxy group also has specific chemical activity. Contact with oxidizing agents and reducing agents can easily trigger redox reactions and cause danger. In case of strong oxidizing agents, the substituents on the benzene ring may be oxidized, destroying its molecular structure.
Third, the transportation process must ensure that the packaging is complete and sealed. If the packaging is damaged, the substance is easy to contact with moisture, oxygen and other substances in the external environment. Moisture may cause side reactions such as hydrolysis of carboxyl groups, and oxygen may oxidize groups such as methoxy groups, affecting product quality. And package damage may also lead to leakage, posing a hazard to transporters and the surrounding environment.
Fourth, the transport vehicle should be equipped with the corresponding variety and quantity of fire fighting equipment and leakage emergency treatment equipment. In the event of leakage or fire and other accidents, emergency treatment can be carried out in time to reduce the harm. In case of fire, according to its chemical characteristics, the appropriate fire extinguishing agent can be selected for fighting.
Fifth, it should be handled lightly and lightly to avoid packaging damage due to collision, friction, etc., which will affect the stability and safety of the substance. In short, 1 - (methoxy) - 3,5 - dicarboxylbenzene needs to strictly follow relevant specifications during storage and transportation to ensure its quality and safety in an all-round way.
First, because of its chemical properties, the storage environment requirements are quite high. It should be placed in a cool, dry and well-ventilated place, and must not be close to fire or heat sources. Because if the substance is heated, it may cause chemical reactions, cause it to deteriorate or pose a safety risk. For example, high temperature may cause reactions such as dehydration of functional groups such as carboxyl groups, affecting their chemical structure and properties.
Second, when storing, it must be stored separately from oxidants and reducing agents, and must not be mixed. The carboxyl group in Gein 1- (methoxy) -3,5-dicarboxylbenzene has a certain acidity, and the methoxy group also has specific chemical activity. Contact with oxidizing agents and reducing agents can easily trigger redox reactions and cause danger. In case of strong oxidizing agents, the substituents on the benzene ring may be oxidized, destroying its molecular structure.
Third, the transportation process must ensure that the packaging is complete and sealed. If the packaging is damaged, the substance is easy to contact with moisture, oxygen and other substances in the external environment. Moisture may cause side reactions such as hydrolysis of carboxyl groups, and oxygen may oxidize groups such as methoxy groups, affecting product quality. And package damage may also lead to leakage, posing a hazard to transporters and the surrounding environment.
Fourth, the transport vehicle should be equipped with the corresponding variety and quantity of fire fighting equipment and leakage emergency treatment equipment. In the event of leakage or fire and other accidents, emergency treatment can be carried out in time to reduce the harm. In case of fire, according to its chemical characteristics, the appropriate fire extinguishing agent can be selected for fighting.
Fifth, it should be handled lightly and lightly to avoid packaging damage due to collision, friction, etc., which will affect the stability and safety of the substance. In short, 1 - (methoxy) - 3,5 - dicarboxylbenzene needs to strictly follow relevant specifications during storage and transportation to ensure its quality and safety in an all-round way.
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