3-Chloro-4,6-dinitroaniline
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- Molecular formula
- C12H7ClN4O4
- CAS Number
- 6317-18-6
- IUPAC Name
- N-(3-chlorophenyl)-2,4-dinitro-aniline
- Molecular Weight
- 265.66g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.5210g/cm3
- Synonyms
- 3'-CHLORO-2, 4-DINITRODIPHENYLAMINE
Identification
Interesting facts
Interesting Facts About N-(3-Chlorophenyl)-2,4-dinitro-aniline
N-(3-chlorophenyl)-2,4-dinitro-aniline, often referred to as a member of the aniline family, is a compound that holds a significant place in both organic chemistry and materials science. Here are some engaging facts about this intriguing compound:
- Functional Groups: This compound contains multiple functional groups, including an aniline group, which is known for its ability to engage in various chemical reactions, making it a valuable intermediate in the synthesis of complex organic molecules.
- Applications: It is commonly used in the production of dyes, pharmaceuticals, and agrochemicals, particularly because the dinitro functionality can impart specific chemical reactivity.
- Color Characteristics: Due to its chemical structure, compounds in this class can often exhibit vivid colors, making them suitable for use as dyes and indicators.
- Environmental Considerations: Like many nitroaniline derivatives, it is important to handle this compound with care due to potential environmental and health impacts, including toxicity. Safety protocols are essential in laboratory settings.
- Synthetic Pathways: The synthesis of N-(3-chlorophenyl)-2,4-dinitro-aniline typically involves nitration and chlorination reactions, showcasing a classic approach in synthetic organic chemistry.
- Structure Activity Relationship (SAR): The presence of both chlorine and nitro groups significantly affects its biological activity, making it a topic of interest in medicinal chemistry and pharmacology.
In conclusion, N-(3-chlorophenyl)-2,4-dinitro-aniline embodies the dynamic interplay of functionality, application, and reactivity typical in the world of organic compounds. As researchers continue to explore its properties and applications, they unlock further potential within organic synthesis and pharmaceutical development.