Interesting facts
Interesting Facts About 3-vinyl-7-oxabicyclo[4.1.0]heptane
3-vinyl-7-oxabicyclo[4.1.0]heptane is a fascinating compound that showcases a unique structural framework, making it a point of interest for chemists and material scientists alike. Here are some engaging aspects of this compound:
- Structural Complexity: This compound features a bicyclic structure, which is characterized by its two interconnected rings. The presence of an oxygen atom in one of the rings adds to its intriguing chemical behavior.
- Potential Applications: Compounds with similar structures can be employed in various applications, including in organic synthesis, in materials science for the development of novel polymers, and even in medicinal chemistry.
- Chemical Reactivity: The vinyl group present in 3-vinyl-7-oxabicyclo[4.1.0]heptane makes this compound particularly reactive. It can participate in addition reactions, allowing for a wide range of chemical transformations.
- Synthesis Pathways: The synthesis of this compound can be quite intricate, often involving multiple steps. Exploring the synthetic routes not only contributes to the understanding of organic chemistry but also enhances the skills necessary for laboratory work.
- Research Potential: Ongoing research on compounds like 3-vinyl-7-oxabicyclo[4.1.0]heptane opens new avenues for discovering novel chemical reactions and pathways, which could lead to groundbreaking applications in various fields.
In summary, 3-vinyl-7-oxabicyclo[4.1.0]heptane stands out due to its structural intricacies and its potential for diverse applications. As one investigates this compound further, it exemplifies the beauty and complexity of organic chemistry, inviting curiosity and innovation.
Synonyms
106-86-5
1,2-Epoxy-4-vinylcyclohexane
3-Vinyl-7-oxabicyclo[4.1.0]heptane
Epoxide 101
4-Vinylcyclohexene oxide
7-Oxabicyclo[4.1.0]heptane, 3-ethenyl-
Unoxat epoxide 101
Vinylcyclohexane monoxide
1-Vinyl-3,4-epoxycyclohexane
4-Vinyl-1,2-epoxycyclohexane
4-Vinylcyclohexene monoxide
3,4-Epoxycyclohexylethylene
4-Vinylcyclohexane monoepoxide
Vinylcyclohexene monoxide
EP-101
4-Vinyl-1-Cyclohexene-1,2-Epoxide
4-Vinylcyclohexene-1,2-epoxide
3-ethenyl-7-oxabicyclo[4.1.0]heptane
4-Vinylcyclohexane, 1,2-epoxide
EINECS 203-436-1
4-Vinyl-1-Cyclohexene 1,2-Epoxide
NSC 35409
3-Vinyl-7-oxabicyclo(4.1.0)heptane
BRN 0107390
7-Oxabicyclo(4.1.0)heptane, 3-ethenyl-
AI3-26045
DTXSID10861725
7-OXABICYCLO(4.1.0)HEPTANE, 3-VINYL-
4-17-00-00314 (Beilstein Handbook Reference)
7-Oxabicyclo[4.1.0]heptane, 3-vinyl-
MFCD00022356
SCHEMBL33100
1,2-epoxy-4-vinyl-cyclohexane
4-Vinylcyclohexane 1,2-epoxide
WLN: T36 BOTJ E1U1
DTXCID50810611
CHEBI:189262
NSC35409
NSC-35409
AKOS015901730
CS-W013521
7-Oxabicyclo4.1.0heptane, 3-ethenyl-
CS-17360
E0956
NS00041291
E70404
3,4-Epoxycyclohexylethylene;1-Vinyl-3,4-epoxycyclohexane;3-Eethehyl-7-oxabicyclo[4.1.0]heptane;3-Vinyl-7-oxabicyclo[4.1.0]heptane;1,2-Epoxy-4-vinylcyclohexane;
Solubility of 3-vinyl-7-oxabicyclo[4.1.0]heptane
3-vinyl-7-oxabicyclo[4.1.0]heptane exhibits a unique solubility profile that is influenced by its molecular structure. This compound shows interesting characteristics based on its polarity and functional groups. Here are some key points regarding its solubility:
In summary, 3-vinyl-7-oxabicyclo[4.1.0]heptane is more soluble in organic solvents while demonstrating minimal solubility in aqueous environments, largely influenced by its structural composition and functional characteristics.