Interesting facts
Interesting Facts about 5-(Bromomethyl)-1,2,3,4,7,7-hexachloro-bicyclo[2.2.1]hept-2-ene
This fascinating compound, often referred to in its abbreviated forms, stands out for several reasons within the domain of organic chemistry. Its unique structure incorporates multiple halogen substitutions, which profoundly influence its chemical behavior and potential applications.
Unique Structural Features
- Bicyclic Framework: The compound contains a bicyclo[2.2.1]heptane core, providing a robust framework that embodies both strength and stability.
- Hexachloro Configuration: The presence of six chlorine atoms showcases its extreme halogenation, which can significantly enhance its reactivity and potential use in various chemical reactions.
- Bromomethyl Group: This important functional group opens doors to further chemical transformations, allowing for the attachment of other functional groups or molecules.
Applications
The compounds that bear such complex halogenated structures typically find roles in fields such as:
- Pesticide Development: Compounds with strong chlorine and bromine atoms can be highly effective as pesticides due to their ability to disrupt biological processes in pests.
- Pharmaceutical Research: Halogenated compounds are often explored for their potential in drug design, as halogens can influence lipophilicity and biological activity.
- Material Science: Due to their stability, halogenated bicyclic compounds may be valuable in synthesizing new materials with desired mechanical and thermal properties.
Reactivity and Synthesis
Understanding the reactivity of this compound can provide insights into:
- Electrophilic Reactions: The highly electron-withdrawing nature of chlorine makes this compound a prime candidate for electrophilic aromatic substitutions.
- Potential Toxicity: The strong bond formation and stability often seen in halogenated compounds raise questions regarding their environmental impact and toxicity, making them subjects of rigorous study.
In labs, continual exploration of such compounds can lead to groundbreaking discoveries, emphasizing the importance of understanding their chemistry as we advance in the field.
Synonyms
Bromocyclen
Bromociclen
1715-40-8
Bromociclene
Bromodan
Alugan
5-(bromomethyl)-1,2,3,4,7,7-hexachlorobicyclo[2.2.1]hept-2-ene
Bromocicleno
DTXSID6041680
CHEBI:82097
Bromomethylhexachlorobicycloheptene
NCGC00166203-01
5-(Bromomethyl)-1,2,3,4,7,7-hexachlorobicyclo(2.2.1)hept-2-ene
DTXCID4021680
CAS-1715-40-8
2-NORBORNENE, 5-(BROMOMETHYL)-1,2,3,4,7,7-HEXACHLORO-
ENT-23393
Bicyclo[2.2.1]hept-2-ene, 5-(bromomethyl)-1,2,3,4,7,7-hexachloro-
Bromodan-d5
SD-2774
SCHEMBL117965
5- Bromomethyl-1,2,3,4,7,7-hexachloro-2-norbornene
CHEMBL1437390
HY-B1567
Tox21_112345
Tox21_301856
ENT 23393
AKOS022181470
Tox21_112345_1
SD 2774
NCGC00166203-02
NCGC00255473-01
DB-043870
CS-0013458
NS00001549
Bromocyclen, PESTANAL(R), analytical standard
C18958
SR-01000883683
Bromomethyl-1,2,3,4,7,7-hexachloro-2-norbornene
SR-01000883683-1
5-(Bromomethyl)-1,2,3,4,7,7-hexachloro-norbornene
Q27155747
Q27281057
(-)-5-ENDO-BROMOMETHYL-1,2,3,4,7,7-HEXACHLORO-2-NORBORNENE
Solubility of 5-(bromomethyl)-1,2,3,4,7,7-hexachloro-bicyclo[2.2.1]hept-2-ene
The solubility of 5-(bromomethyl)-1,2,3,4,7,7-hexachloro-bicyclo[2.2.1]hept-2-ene in various solvents showcases its interesting chemical behavior. Understanding its solubility characteristics is essential for applications in chemical synthesis and material science. Here are some key points to consider:
In summary, the solubility of 5-(bromomethyl)-1,2,3,4,7,7-hexachloro-bicyclo[2.2.1]hept-2-ene can be summarized as follows:
Understanding these factors can greatly enhance practical applications and inform further research on the compound's behavior in various chemical environments.