2-Chloro-3-nitrobenzoic acid
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- Molecular formula
- C7H4ClNO4
- CAS Number
- 1634-84-4
- IUPAC Name
- 2-chloro-3-nitro-benzoic acid
- Molecular Weight
- 201.57g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.6100g/cm3
- Synonyms
- 2-CHLORO-3-NITROBENZOIC ACID
Identification
Interesting facts
Interesting Facts about 2-Chloro-3-Nitro-Benzoic Acid
2-Chloro-3-nitro-benzoic acid is an intriguing compound that has garnered attention in various fields of chemistry. Here are some fascinating aspects of this chemical:
- Reactivity: This compound is known for its remarkable reactivity due to the presence of electron-withdrawing groups (the chloro and nitro groups). This makes it an essential starting material in the synthesis of various organic compounds.
- Applications: 2-Chloro-3-nitro-benzoic acid is utilized in the development of pharmaceuticals, agrochemicals, and other fine chemicals. Its derivatives play a role in producing dyes and pigments.
- Biological Activity: Research has indicated that this compound exhibits some promising biological activities. Some studies suggest potential antimicrobial and anti-inflammatory properties, making it an area of interest for medicinal chemistry.
- Synthetic Pathways: The synthesis of 2-chloro-3-nitro-benzoic acid can be achieved through various pathways, such as nitration of 2-chlorobenzoic acid. Understanding its synthesis is critical for chemists looking to produce this compound efficiently.
- Structural Insights: The molecular structure consists of a benzoic acid backbone, providing unique characteristics to the compound. The positioning of the chloro and nitro groups on the aromatic ring can significantly affect the compound's properties and reactivity.
In conclusion, 2-chloro-3-nitro-benzoic acid is a compound that presents numerous opportunities for exploration in organic chemistry, making it easier for students and researchers alike to appreciate its potential.