2-[4-bromo-2-(diethylaminomethyl)phenoxy]acetohydrazide
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- Molecular formula
- C13H19BrN2O2
- CAS Number
- 102886-98-4
- IUPAC Name
- 2-[4-bromo-2-(diethylaminomethyl)phenoxy]acetohydrazide
- Molecular Weight
- 330.21g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3700g/cm3
- Appearance
- depending on the purity and form (such as amorphous or crystalline) of the sample.
- Synonyms
- 16158-14-8
Identification
Interesting facts
Interesting Facts about 2-[4-bromo-2-(diethylaminomethyl)phenoxy]acetohydrazide
2-[4-bromo-2-(diethylaminomethyl)phenoxy]acetohydrazide is a fascinating compound that has garnered attention in both chemical research and potential therapeutic applications. Below are some intriguing insights into this compound:
- Dual Functional Groups: This compound features both an acetohydrazide moiety and a bromo-substituted phenoxy structure, which makes it a versatile scaffold for further chemical modifications.
- Pharmacological Potential: Compounds with hydrazide linkages have been studied for their biological activities, including potential use as anti-cancer agents. The presence of the diethylaminomethyl group may enhance its interaction with biological targets.
- Electrophilic Character: The bromine atom in the compound can act as a leaving group in nucleophilic substitution reactions, making it an excellent candidate for further derivatization.
- Synthetic Pathways: This compound can be synthesized through multiple synthetic routes, allowing for the creation of various analogs. Students and chemists find this flexibility in synthesis to be particularly appealing.
- Research Applications: Due to its unique structure, this compound is of interest in fields such as medicinal chemistry, where researchers explore its potential as a lead compound for drug development.
As a chemist, encountering compounds like 2-[4-bromo-2-(diethylaminomethyl)phenoxy]acetohydrazide broadens our understanding of chemical reactivity and potential applications. This compound exemplifies the importance of modifying well-established structures to innovate and discover new therapeutic avenues.