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Description
2-Chloro-1,4-naphthoquinone is a chemical compound widely used in laboratory settings for its versatile reactivity and structural stability. It belongs to the class of aromatic compounds and is commonly employed in organic synthesis due to its ability to participate in various chemical reactions. This compound serves as a building block for the development of more complex molecules, making it an essential tool in synthetic chemistry. Its presence in laboratory experiments is particularly notable in oxidation and reduction reactions, where it acts as a key intermediate.
The compound's reactivity and aromatic structure make it a preferred choice for researchers. It exhibits strong chemical stability under specific conditions and can react with a variety of functional groups such as amines, alcohols, and acids. These properties allow it to be used in the synthesis of biologically active compounds, including those with pharmaceutical or industrial applications. Its ability to engage in multiple reaction pathways enhances its utility in both academic and applied research environments.
In Indonesian laboratories, 2-Chloro-1,4-naphthoquinone is a popular reagent in organic chemistry research. It is frequently used in the development of new compounds with potential applications in drug discovery or material science. Its availability and reliability in chemical reactions make it a valuable resource for scientists working in diverse research fields. The compound's consistent performance supports its widespread use in both teaching and applied research settings.
Laboratory Applications
Organic synthesis is a primary application where 2-Chloro-1,4-naphthoquinone is used to build complex molecules due to its reactivity and aromatic structure.
Oxidation and reduction reactions benefit from this compound's ability to act as an intermediate, enabling the formation of various functional groups.
Biologically active compound development relies on its capacity to participate in reactions that yield compounds with pharmaceutical or industrial potential.
Teaching laboratories utilize it as an educational tool to demonstrate chemical reactivity and synthetic pathways in organic chemistry.
Industrial research applications leverage its stability and versatility for the creation of new materials or chemical products.
Specifications
Brand: TCI
CAS number: 1010-60-2
Category: Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes: As available from supplier
Physical form: Solid
Storage note: Store in a cool, dry place away from light and moisture
Handling and Storage
2-Chloro-1,4-naphthoquinone should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air and humidity, which may affect its reactivity. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. The compound is not classified as hazardous under standard laboratory conditions, but standard chemical handling protocols should be followed. It is important to keep the substance in a well-ventilated area and avoid contact with incompatible materials. Proper storage and handling practices help preserve its effectiveness and ensure safe usage in laboratory settings.
