1-Chloro-2,4-dimethoxy-5-nitrobenzene, despite its complex chemical name, has practical applications in everyday life. This compound is commonly used in the pharmaceutical industry as a building block for various drugs and medications. It serves as a key intermediate in the synthesis of several important pharmaceuticals, contributing to the development of new treatments for various medical conditions. Therefore, the relevance of 1-Chloro-2,4-dimethoxy-5-nitrobenzene lies in its instrumental role in advancing healthcare and improving the quality of life for individuals around the world.
Table of Contents:
- 💡 Commercial Applications
- ⚗️ Chemical & Physical Properties
- 🏭 Production & Procurement
- ⚠️ Safety Considerations
- 🔬 Potential Research Directions
- 🧪 Related Compounds
💡 Commercial Applications
1-Chloro-2,4-dimethoxy-5-nitrobenzene has various commercial and industrial applications. It is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, it is utilized in the production of dyes, antioxidants, and other specialty chemicals.
In the pharmaceutical industry, 1-Chloro-2,4-dimethoxy-5-nitrobenzene is a key ingredient in the manufacturing of certain drugs and medications. It is often employed in the synthesis of antibacterial agents, antifungal medications, and other pharmaceutical compounds. Its unique chemical properties make it a valuable component in drug development processes.
Furthermore, 1-Chloro-2,4-dimethoxy-5-nitrobenzene is also used in the production of herbicides and pesticides, making it an essential compound in the agricultural sector. Its ability to act as a building block for various chemicals and compounds makes it a versatile and important component in both commercial and industrial settings.
⚗️ Chemical & Physical Properties
1-Chloro-2,4-dimethoxy-5-nitrobenzene appears as a colorless liquid with a faint odor. Its scent is slightly reminiscent of chlorine due to the presence of the chlorine atom in its chemical structure.
The molar mass of 1-Chloro-2,4-dimethoxy-5-nitrobenzene is approximately 245.60 g/mol, and its density is around 1.36 g/cm3. Compared to common food items, such as sugar (molar mass of 342.30 g/mol, density of 1.59 g/cm3) and salt (molar mass of 58.44 g/mol, density of 2.16 g/cm3), this compound has a lower molar mass and density.
The melting point of 1-Chloro-2,4-dimethoxy-5-nitrobenzene is approximately 58-60°C, while its boiling point is around 244-246°C. In comparison, common food items like butter (melting point of 30-35°C, boiling point of 177°C) and chocolate (melting point of 30-32°C, boiling point of 160°C) have lower melting and boiling points.
1-Chloro-2,4-dimethoxy-5-nitrobenzene is sparingly soluble in water, but it exhibits low viscosity as a liquid. This differs from common food items like salt and sugar, which are highly soluble in water and have higher viscosity when dissolved.
🏭 Production & Procurement
1-Chloro-2,4-dimethoxy-5-nitrobenzene is typically produced through a multistep synthetic route starting from readily available starting materials. The synthesis involves a series of chemical reactions such as chlorination, methylation, and nitration to introduce the desired functional groups onto the benzene ring. This process requires careful control of reaction conditions and purification steps to obtain high yield and purity of the final product.
The procurement of 1-Chloro-2,4-dimethoxy-5-nitrobenzene can be accomplished through chemical suppliers specializing in rare and specialty chemicals. The compound is usually available in the form of a solid powder or crystalline material. It is important to handle and store the compound in accordance with safety guidelines due to its chemical reactivity and potential hazards. Transportation of 1-Chloro-2,4-dimethoxy-5-nitrobenzene should be done in compliance with regulations for hazardous materials to ensure safe delivery to the end user.
Once procured, 1-Chloro-2,4-dimethoxy-5-nitrobenzene can be stored in a cool, dry place away from direct sunlight and sources of heat or ignition. Proper labeling of the container with safety information and handling instructions is essential to prevent accidents or mishandling. Care should be taken when handling the compound to avoid exposure to skin, eyes, or inhalation of vapors. It is recommended to use appropriate personal protective equipment and follow established safety protocols when working with 1-Chloro-2,4-dimethoxy-5-nitrobenzene.
⚠️ Safety Considerations
Safety considerations for 1-Chloro-2,4-dimethoxy-5-nitrobenzene must be taken seriously due to its potential hazards. This compound is classified as harmful if swallowed, inhaled, or in contact with skin, and may cause skin and eye irritation. It is also considered harmful to aquatic life with long-lasting effects. Therefore, it is imperative to handle this chemical with caution and use appropriate personal protective equipment, such as gloves and goggles, when working with it.
Additionally, proper storage and handling of 1-Chloro-2,4-dimethoxy-5-nitrobenzene is crucial to prevent accidents and ensure safety. This compound should be kept in a well-ventilated area away from heat sources and incompatible materials. It should also be stored in a tightly sealed container in a cool, dry place, and should not be allowed to come into contact with strong oxidizing agents or reducing agents.
In case of accidental exposure or ingestion of 1-Chloro-2,4-dimethoxy-5-nitrobenzene, immediate medical attention should be sought. It is important to provide the medical personnel with all relevant information about the compound, including its chemical name and CAS number, to ensure appropriate treatment.
The hazard statements for 1-Chloro-2,4-dimethoxy-5-nitrobenzene include “Harmful if swallowed,” “Causes skin irritation,” “Causes serious eye irritation,” and “Toxic to aquatic life with long-lasting effects.” These statements indicate the potential risks associated with this compound and emphasize the need for proper handling and storage to prevent harm to humans and the environment.
Precautionary statements for 1-Chloro-2,4-dimethoxy-5-nitrobenzene include “Avoid breathing dust/fume/gas/mist/vapors/spray,” “Wear protective gloves/protective clothing/eye protection/face protection,” “IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing,” and “Dispose of contents/container in accordance with local/regional/national/international regulations.” These statements provide guidelines for safe handling and disposal of the compound to minimize the risk of exposure and environmental contamination.
🔬 Potential Research Directions
Potential research directions for 1-Chloro-2,4-dimethoxy-5-nitrobenzene may include investigations into its chemical properties and reactivity. This compound’s unique structure, with both electron-withdrawing and electron-donating groups, could make it a subject of interest for studies on organic reactions and synthesis.
Furthermore, studies on the biological activities and potential pharmacological applications of 1-Chloro-2,4-dimethoxy-5-nitrobenzene could be pursued. Its nitro and chloro substituents may confer specific interactions with biological targets, making it a potential lead compound for drug development.
Additionally, research into the environmental fate and effects of 1-Chloro-2,4-dimethoxy-5-nitrobenzene could be of importance. Understanding its behavior in the environment, as well as its toxicity to organisms, can contribute to assessments of its risk and potential impact on ecosystems.
🧪 Related Compounds
One similar compound to 1-Chloro-2,4-dimethoxy-5-nitrobenzene is 1-Bromo-2,4-dimethoxy-5-nitrobenzene. This compound shares a similar structure with the chlorine atom being replaced by a bromine atom. The bromine atom also belongs to the halogen group, making this compound a suitable candidate for comparison with 1-Chloro-2,4-dimethoxy-5-nitrobenzene.
Another comparable compound is 1-Chloro-2,4-dimethoxy-3-nitrobenzene. This compound differs from the original due to the location of the nitro group on the benzene ring. The presence of the chlorine substituent and the methoxy groups remains consistent across these two compounds, allowing for a straightforward comparison of their properties and reactivity.
