2,6-Dibromo-4-(chloroimino)cyclohexa-2,5-dienone 

2,6-Dibromo-4-(chloroimino)cyclohexa-2,5-dienone, a compound commonly known as DBA, has relevance in everyday life due to its antimicrobial properties. It is widely used in the healthcare industry for its ability to prevent the growth of harmful bacteria and fungi. In addition, DBA is also utilized in the manufacturing of certain pharmaceutical products and personal care items. Its significance lies in its contribution to enhancing public health and hygiene measures.

Table of Contents:

💡  Commercial Applications

One of the main commercial and industrial applications of 2,6-Dibromo-4-(chloroimino)cyclohexa-2,5-dienone is its use as a reagent in organic synthesis. It is commonly used in the production of various chemical compounds in the pharmaceutical, agricultural, and fragrance industries due to its role as a versatile building block.

Additionally, 2,6-Dibromo-4-(chloroimino)cyclohexa-2,5-dienone has found applications in the field of material science. It is used as a precursor in the synthesis of polymers, coatings, and adhesives due to its unique chemical properties and ability to impart specific characteristics to the final product.

In the realm of drug and medication applications, 2,6-Dibromo-4-(chloroimino)cyclohexa-2,5-dienone is utilized as a key intermediate in the synthesis of pharmaceutical compounds. It serves as a crucial starting material for the development of drugs targeting various medical conditions, showcasing its importance in the healthcare industry.

⚗️  Chemical & Physical Properties

2,6-Dibromo-4-(chloroimino)cyclohexa-2,5-dienone is a solid compound with a pale yellow color and a faint odor. It is typically found in crystalline form, with a slight chlorine scent detectable upon close inspection.

With a molar mass of 352.82 g/mol and a density of 2.228 g/cm³, 2,6-Dibromo-4-(chloroimino)cyclohexa-2,5-dienone is much heavier and denser than common food items. For comparison, water has a molar mass of 18.015 g/mol and a density of 1 g/cm³.

This compound has a melting point of 152-155°C and a boiling point of 415.6°C. These values are significantly higher than those of common food items like sugar and salt, which have much lower melting and boiling points.

2,6-Dibromo-4-(chloroimino)cyclohexa-2,5-dienone is sparingly soluble in water and exhibits a low viscosity. In comparison to common food items like sugar and salt, which are highly soluble in water and have varying viscosities, this compound displays different solubility and viscosity characteristics.

🏭  Production & Procurement

2,6-Dibromo-4-(chloroimino)cyclohexa-2,5-dienone is typically produced through a series of synthetic reactions involving the bromination of 4-chlorocyclohexa-2,5-dienone. This compound is then subjected to a series of further reactions to introduce the necessary functional groups, ultimately yielding 2,6-Dibromo-4-(chloroimino)cyclohexa-2,5-dienone.

2,6-Dibromo-4-(chloroimino)cyclohexa-2,5-dienone can be procured from chemical suppliers specializing in rare and specialized compounds. Due to its complex structure and limited availability, this compound may need to be ordered in advance and shipped under controlled conditions to ensure its stability and purity during transportation.

When transporting 2,6-Dibromo-4-(chloroimino)cyclohexa-2,5-dienone, it is essential to adhere to strict safety guidelines and regulations to prevent any accidents or contamination. Proper labeling, packaging, and handling procedures should be followed to ensure the compound reaches its destination safely and without any degradation in quality.

⚠️  Safety Considerations

Safety considerations for 2,6-Dibromo-4-(chloroimino)cyclohexa-2,5-dienone should be taken seriously due to its potential health hazards. This compound may cause skin and eye irritation upon contact, and inhalation or ingestion can lead to respiratory irritation, nausea, and vomiting. It is essential to handle this chemical with caution, wearing appropriate personal protective equipment such as gloves, safety goggles, and a lab coat to prevent exposure.

Hazard statements for 2,6-Dibromo-4-(chloroimino)cyclohexa-2,5-dienone include “Causes skin and eye irritation,” “May cause respiratory irritation,” and “Harmful if swallowed.” These statements highlight the potential risks associated with this compound and emphasize the importance of proper handling and storage to prevent health hazards. It is crucial to follow safety guidelines and protocols when working with this chemical to minimize the risk of exposure and adverse effects.

Precautionary statements for 2,6-Dibromo-4-(chloroimino)cyclohexa-2,5-dienone include “Wear protective gloves/eye protection/face protection,” “IF SWALLOWED: Rinse mouth. Do NOT induce vomiting,” and “IF IN EYES: Rinse cautiously with water for several minutes.” These statements provide specific instructions on how to handle exposure incidents and outline the necessary steps to take in case of accidental contact with the chemical. It is vital to familiarize oneself with these precautionary measures and follow them diligently to ensure personal safety and minimize the potential risks associated with 2,6-Dibromo-4-(chloroimino)cyclohexa-2,5-dienone.

🔬  Potential Research Directions

One potential research direction for 2,6-Dibromo-4-(chloroimino)cyclohexa-2,5-dienone could involve investigating its pharmacological properties and potential applications in drug discovery. Studies could focus on the compound’s interaction with biological targets and its ability to modulate various biological processes.

Another research avenue could explore the synthesis and modification of 2,6-Dibromo-4-(chloroimino)cyclohexa-2,5-dienone derivatives to enhance its chemical and physical properties. This could involve the development of novel synthetic strategies to access a diverse range of analogs with improved stability, solubility, and bioavailability.

Additionally, investigations into the environmental impact of 2,6-Dibromo-4-(chloroimino)cyclohexa-2,5-dienone and its derivatives could be a worthwhile research direction. Studies could evaluate the compound’s persistence, bioaccumulation potential, and toxicity in different ecosystems to assess its potential risks and inform regulatory decisions.

One similar compound to 2,6-Dibromo-4-(chloroimino)cyclohexa-2,5-dienone based on its molecular structure is 2,6-Dibromo-4-(fluoroimino)cyclohexa-2,5-dienone. In this compound, the chlorine atom in the chloroimino group is replaced with a fluorine atom. This substitution results in a compound with similar reactivity and physical properties, but with the fluorine atom providing distinct characteristics.

Another comparable compound is 2,6-Dibromo-4-(methylimino)cyclohexa-2,5-dienone. In this molecule, the chlorine atom is replaced with a methyl group attached to the imino nitrogen atom. This substitution introduces a different functional group to the compound, leading to potential changes in its chemical behavior and biological activity. The presence of the methyl group may influence the compound’s solubility, stability, and interactions with other molecules.

A related compound is 2,6-Dibromo-4-(phenylimino)cyclohexa-2,5-dienone. Here, the chlorine atom is substituted with a phenyl group connected to the imino nitrogen atom. This alteration introduces aromaticity to the compound, potentially affecting its electronic properties and reactivity. The presence of the phenyl group may also influence the compound’s ability to interact with biological targets or exhibit specific pharmacological effects.

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