3,5-Dichloro-N-(1,1-dimethylprop-2-ynyl)benzamide
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- Molecular formula
- C12H11Cl2NO
- CAS Number
- 101389-84-4
- IUPAC Name
- 3,5-dichloro-N-(1,1-dimethylprop-2-ynyl)benzamide
- Molecular Weight
- 255.12g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3030g/cm3
- Appearance
- typically includes a crystalline structure and is often encountered as a powder. The solid is generally white to off-white in color.
- Synonyms
- Propyzamide
Identification
Interesting facts
Interesting Facts about 3,5-Dichloro-N-(1,1-dimethylprop-2-ynyl)benzamide
3,5-Dichloro-N-(1,1-dimethylprop-2-ynyl)benzamide is a fascinating compound known for its unique structural characteristics and applications in various fields. Here are some intriguing aspects of this chemical:
- Biological Activity: The compound has been studied for its potential therapeutic effects, particularly in the realm of pharmaceutical chemistry. Its formulation often explores its capacity as a selective inhibitor, which can be crucial in the development of targeted treatments.
- Structural Complexity: This compound contains a benzamide moiety, which is associated with numerous biologically active agents. The presence of multiple chlorine atoms enhances its reactivity and allows for a diversified range of chemical interactions, making it a molecule of interest for synthetic chemists.
- Synthesis Considerations: The synthesis of 3,5-dichloro-N-(1,1-dimethylprop-2-ynyl)benzamide can involve intricate multi-step reactions, illustrating the creativity required in organic synthesis. Researchers often utilize this compound as a benchmark for new synthetic strategies.
- Applications in Agrochemicals: Beyond pharmaceuticals, there is a growing interest in this compound's potential use in agrochemicals. The chlorinated structure could provide the stability and efficacy needed for pest control formulations.
- Research Implications: Scientists are continually exploring the implications of variations within the compound's structure. Studies may focus on modifying the groups attached to the benzamide, which can result in compounds with significantly different properties and activities.
As noted by a renowned chemist, "Understanding the nuances of molecular interactions at this level is what drives innovation." This sentiment rings true with compounds like 3,5-dichloro-N-(1,1-dimethylprop-2-ynyl)benzamide, as they represent the intersection of creativity and rigorous scientific inquiry.
In the context of materials science, this compound demonstrates how synthetic modifications can lead to enhanced material properties, paving the way for future research and applications.