Interesting facts
Interesting Facts about 1,2-Dibromo-4-(1,2-dibromoethyl)cyclohexane
1,2-Dibromo-4-(1,2-dibromoethyl)cyclohexane is a fascinating organic compound with unique properties and various applications in the field of chemistry. Here are some engaging insights into this compound:
- Bromination Reaction: This compound features multiple bromine substituents, which makes it a notable example of a halogenated alkane. The presence of bromine atoms can significantly alter the reactivity and physical properties of the parent hydrocarbon.
- Structural Diversity: It possesses a cyclohexane ring structure with important functional groups. The incorporation of these bromine atoms introduces chirality and opens up avenues for stereoisomerism, contributing to its chemical complexity.
- Applications in Research: Compounds like 1,2-dibromo-4-(1,2-dibromoethyl)cyclohexane are valuable in organic synthesis, including the development of pharmaceuticals. Their unique reactivity can be harnessed for creating more complex molecules through reactions such as nucleophilic substitution and elimination.
- Environmental Considerations: Brominated compounds have raised ecological concerns due to their persistence in the environment and potential for bioaccumulation. This emphasizes the importance of responsible use and disposal in research and industrial applications.
- Physical Interaction: The spatial arrangement of the bromine atoms affects the molecular interactions, influencing properties like solubility and reactivity. Understanding these interactions is crucial for chemists when designing experiments and new materials.
This compounds' intriguing structure and properties make it a significant subject of study for chemists interested in synthesis, environmental impact, and molecular behavior. As emphasized by many scientists, “The study of such compounds not only uncovers the fundamental principles of chemistry but also fosters innovative applications in various industries.”
Synonyms
1,2-DIBROMO-4-(1,2-DIBROMOETHYL)CYCLOHEXANE
Cyclohexane, 1,2-dibromo-4-(1,2-dibromoethyl)-
1-(1,2-Dibromoethyl)-3,4-dibromocyclohexane
CCRIS 3743
BCH cyclohexane compound
HSDB 6146
EINECS 222-036-8
BRN 1927455
DTXSID8024947
UNII-502D5Q149T
DTXCID204947
3-05-00-00093 (Beilstein Handbook Reference)
1-(1,2-DIBROMOETHYL)-3,4-DIBROMOCYCLOHEXANE [HSDB]
TBECH cpd
1(1,2Dibromoethyl)3,4dibromocyclohexane
4(1,2Dibromoethyl)1,2dibromocyclohexane
Cyclohexane, 1,2dibromo4(1,2dibromoethyl)
CYCLOHEXANE, 1,2-DIBROMO-4-(1,2-DIBROMOMETHYL)-
pqrrsjblkopvjv-uhfffaoysa-n
3322-93-8
Citex BCL 462
Saytex BCL 462
Vinylcyclohexene tetrabromide
4-(1,2-Dibromoethyl)-1,2-dibromocyclohexane
MFCD00086864
CHEMBL375107
502D5Q149T
1,2-DIBROMO-4-(1,2-DIBROMOETHYL)-CYCLOHEXANE
C8H12Br4
MLS002454355
SCHEMBL332771
HMS3039D13
Tox21_200970
BDBM50199965
AKOS015919789
AB89760
NCGC00091838-01
NCGC00091838-02
NCGC00258523-01
DA-17788
DS-17528
PD179167
SMR001371982
SY102311
CAS-3322-93-8
CS-0186287
NS00005516
F11583
Q20054503
1,2-Dibromo-4-(1,2-dibromoethyl)cyclohexane (TBECH)
1beta,2beta-Dibromo-4beta-(1,2-dibromoethyl)cyclohexane
1alpha,2alpha-Dibromo-4alpha-(1,2-dibromoethyl)cyclohexane
Solubility of 1,2-dibromo-4-(1,2-dibromoethyl)cyclohexane
1,2-dibromo-4-(1,2-dibromoethyl)cyclohexane exhibits intriguing solubility characteristics owing to its unique structural features. The presence of multiple bromine atoms contributes to the compound's polarity, which impacts its interaction with solvents.
When considering solubility, it's crucial to note the following:
As a result, one might summarize that “like dissolves like” applies effectively here: 1,2-dibromo-4-(1,2-dibromoethyl)cyclohexane will dissolve best in non-polar environments while showing minimal solubility in more polar settings. This implies a careful selection of solvents is essential for any practical applications involving this compound.