Interesting facts
Interesting Facts about 2-(2-bromoacetyl)oxyethyl 2-bromoacetate
2-(2-bromoacetyl)oxyethyl 2-bromoacetate is a fascinating compound with unique properties and applications in various fields of research. Here are some noteworthy points about this intriguing molecule:
- Reactivity: This compound contains bromoacetyl groups, which are known for their reactivity in organic synthesis. These reactive functional groups can be used in the formation of more complex molecules through nucleophilic substitution reactions.
- Applications in Drug Development: Compounds with bromoacetyl moieties are often investigated for their potential therapeutic effects. Researchers explore their efficacy as intermediates in drug design, particularly in the development of anticancer and antimicrobial agents.
- Use in Polymer Chemistry: 2-(2-bromoacetyl)oxyethyl 2-bromoacetate can be utilized as a monomer in the synthesis of polymers, contributing to the creation of materials with tailored properties for various industrial applications.
- Analytical Interest: The presence of bromo groups makes this compound an excellent candidate for various spectroscopic studies. Techniques such as NMR and IR spectroscopy can provide detailed insights into its structure and dynamics.
- Environmental Impact: Understanding the behavior of this compound in environmental contexts can shed light on its persistence and potential bioaccumulation, raising important questions regarding safety and regulatory measures in chemical usage.
As stated in a recent research review, "the integration of halogenated compounds in chemical synthesis continues to expand the toolbox available for chemists, allowing for innovative approaches in both fundamental and applied chemistry."
This compound serves as a reminder of the vast possibilities within organic chemistry, linking synthetic methodologies with real-world applications. As such, it is a subject of interest for scientists and students alike, driving the exploration of new frontiers in both research and application.
Synonyms
3785-34-0
Ethylene bromoacetate
1,2-Bis(bromoacetoxy)ethane
Pandurol
Acetic acid, bromo-, 1,2-ethanediyl ester
Ethylene bis(bromoacetate)
1,2-Ethanediyl bromoacetate
Ethylene glycol, bis(bromoacetate)
Acetic acid, bromo-, ethylene ester
Bromoacetic acid ethylene ester
Bromoacetic acid 1,2-ethanediyl ester
EINECS 223-250-4
8PU1YB2O2T
NSC 25854
NSC 406054
BRN 1782335
AI3-18935
ACETIC ACID, BROMO-, DIESTER with ETHYLENE GLYCOL
NSC-25854
NSC-406054
1,2-BIS(MONOBROMOACETOXY)ETHANE
DTXSID20191282
1-02-00-00097 (Beilstein Handbook Reference)
DTXCID30113773
Acetic acid, bromo-, ethylene ester (8CI)
Acetic acid, bromo-, 1,2-ethanediyl ester (9CI)
223-250-4
Ethane-1,2-diyl bis(2-bromoacetate)
2-(2-bromoacetyl)oxyethyl 2-bromoacetate
S 13
WLN: E1VO2OV1E
Bromoacetic acid, ethylene ester
UNII-8PU1YB2O2T
Ethanediol bis(2-bromoacetate)
SCHEMBL1434603
WGHAPLWNJPAJDE-UHFFFAOYSA-N
NSC25854
Ethane-1,2-diylbis(2-bromoacetate)
NSC406054
AKOS015964337
AS-75620
NS00030303
D97238
Q27270866
Solubility of 2-(2-bromoacetyl)oxyethyl 2-bromoacetate
When discussing the solubility of 2-(2-bromoacetyl)oxyethyl 2-bromoacetate, several factors come into play that can influence its behavior in different solvents. Here are some key points to consider:
In summary, while definitive solubility data may not be readily available, the compound is expected to exhibit significant solubility in polar solvents and potentially limited solubility in non-polar solvents. Understanding these interactions can provide deeper insights into its practical applications in chemical processes.