Interesting facts
Interesting Facts About 2,4,6-Trinitrobenzoyl Chloride
2,4,6-Trinitrobenzoyl chloride, often abbreviated as TNBC, is a fascinating compound that belongs to the family of nitro-substituted aromatic compounds. Its unique structure and reactivity make it an important subject of study in both organic chemistry and materials science. Here are some intriguing facts about TNBC:
- Reactivity: As a versatile intermediate, 2,4,6-trinitrobenzoyl chloride can participate in various chemical reactions, including acylation, making it valuable for synthesizing more complex organic molecules.
- Unyielding Stability: The presence of multiple nitro groups provides significant stability, but they also increase the compound’s potential for nitration reactions, influencing its reactivity dramatically.
- Role in Synthesis: This compound is often utilized in the synthesis of other organic compounds, particularly in the development of pesticides and pharmaceuticals, showcasing its practical importance in industrial chemistry.
- Environmental Implications: The use of TNBC and similar compounds in industry raises awareness regarding their environmental impacts, emphasizing the need for sustainable practices in chemical manufacturing.
- Historical Context: This compound has roots in historical research on explosives, tying into the broader narrative of how chemical discoveries have shaped modern warfare and industry.
Overall, 2,4,6-trinitrobenzoyl chloride is not just a compound of theoretical interest; it has practical implications and applications that resonate through industries and environmental concerns alike. As we continue to explore its chemistry, we uncover more about its potential uses and effects on our world.
Synonyms
2,4,6-Trinitrobenzoyl chloride
Trinitrobenzoyl chloride (VAN)
BENZOYL CHLORIDE, 2,4,6-TRINITRO-
Trinitrobenzoyl chloride
3YQ5NP3QUV
NSC 408026
BRN 1916188
AI3-19900
NSC-408026
DTXSID60225959
4-09-00-01363 (Beilstein Handbook Reference)
DTXCID40148450
7500-86-9
2,4,6-Trinitrobenzoylchloride
UNII-3YQ5NP3QUV
2,6-Trinitrobenzoyl chloride
WLN: WNR BVG CNW ENW
SCHEMBL3327506
Benzoyl chloride,4,6-trinitro-
MWGGWCCALVNFPN-UHFFFAOYSA-N
MFCD01664374
NSC408026
AKOS003652283
Solubility of 2,4,6-trinitrobenzoyl chloride
2,4,6-trinitrobenzoyl chloride, with the chemical formula C7H3ClN3O5, showcases a unique solubility profile that is essential for its applications in chemical synthesis and various industries.
The solubility characteristics of this compound can be outlined as follows:
Due to its hydrophobic nature, 2,4,6-trinitrobenzoyl chloride is typically handled in anhydrous conditions to avoid complications that arise from moisture. This is notably important in processes where the compound's reactivity is utilized.
In summary, understanding the solubility of 2,4,6-trinitrobenzoyl chloride is crucial for its effective application in chemical reactions and laboratory settings, providing insights into how to maximize its utility while minimizing potential hazards.