Interesting facts
Interesting Facts about 3-(oxiran-2-yl)-7-oxabicyclo[4.1.0]heptane
3-(oxiran-2-yl)-7-oxabicyclo[4.1.0]heptane is a fascinating compound that captures the attention of chemists due to its unique structural features and the intriguing properties that arise from them. Here are some notable points about this compound:
- Complex Structure: The presence of both an epoxide group and a bicyclic system makes this compound a wonderful example of bicyclic chemistry to explore. Bicyclic compounds can exhibit interesting reactivity due to the inherent strain in their structures.
- Reactivity: The epoxide functional group is known for its ability to undergo a variety of ring-opening reactions, leading to the formation of different derivatives. This feature makes it a valuable precursor in organic synthesis.
- Applications: Compounds similar to 3-(oxiran-2-yl)-7-oxabicyclo[4.1.0]heptane have potential applications in the development of pharmaceuticals and agrochemicals, where their unique reactivities can be harnessed for targeted applications.
- Isomerism: The compound may exhibit chirality, leading to the existence of enantiomers and diastereomers. This opens up an avenue for studying stereochemistry and its impact on the physicochemical properties.
- Importance in Research: Due to its complex nature, this compound serves as an interesting subject for research in materials science and medicinal chemistry, where understanding its behavior can lead to innovative solutions.
In summary, 3-(oxiran-2-yl)-7-oxabicyclo[4.1.0]heptane is not just a chemical compound; it represents a blend of intriguing reactivity, structural complexity, and potential practical applications. As chemists delve deeper into its properties, we may uncover even more possibilities that lie within its molecular architecture.
Synonyms
4-Vinylcyclohexene dioxide
106-87-6
4-Vinyl-1-cyclohexene dioxide
4-Vinylcyclohexene diepoxide
VINYLCYCLOHEXENE DIOXIDE
3-(oxiran-2-yl)-7-oxabicyclo[4.1.0]heptane
4-Vinyl-1-cyclohexene diepoxide
Vinyl cyclohexene dioxide
Vinyl cyclohexene diepoxide
1-Vinyl-3-cyclohexene dioxide
1-Ethyleneoxy-3,4-epoxycyclohexane
1-Epoxyethyl-3,4-epoxycyclohexane
Chissonox 206
7-Oxabicyclo[4.1.0]heptane, 3-oxiranyl-
4-Vinyl-1,2-cyclohexene diepoxide
Unox epoxide 206
Chissonox 206 monomer
Vinylcyclohexene Diepoxide
4-Vinlycyclohexene dioxide
4-(Epoxyethyl)-7-oxabicyclo(4.1.0)heptane
3-Oxiranyl-7-oxabicyclo(4.1.0)heptane
EP-206
1,2-Epoxy-4-(epoxyethyl)cyclohexane
4-(1,2-Epoxyethyl)-7-oxabicyclo(4.1.0)heptane
3-(Epoxyethyl)-7-oxabicyclo(4.1.0)heptane
Erla-2270
Erla-2271
3-(1,2-Epoxyethyl)-7-oxabicyclo(4.1.0)heptane
CCRIS 278
NSC 54752
CHEBI:59001
HSDB 4332
NCI-C60135
NCI-C60139
Unox 4206
EINECS 203-437-7
UCET textile finish 11-74 (Obs.)
7-Oxabicyclo(4.1.0)heptane, 3-(epoxyethyl)-
BRN 0106071
25086-25-3
Cyclohexane, 1,2-epoxy-4-(epoxyethyl)-
DTXSID0020604
AI3-26353
7-Oxabicyclo(4.1.0)heptane, 3-oxiranyl-
NSC-7583
NSC-54752
NSC-61281
1-(Epoxyethyl)-3,4-epoxycyclohexane
596C064IG4
3-(1,2-Epoxyethyl)-7-oxabicyclo[4.1.0]heptane
7-Oxa-3-oxiranylbicyclo(4.1.0)heptane
DTXCID80604
RD4
3-(Epoxyethyl)-7-oxabicyclo[4.1.0]heptane
3-oxiran-2-yl-7-oxabicyclo[4.1.0]heptane
NSC7583
7-Oxabicyclo[4.1.0]heptane, 3-(epoxyethyl)-
7-Oxabicyclo(4.1.0)heptane, 3-(2-oxiranyl)-
5-19-01-00295 (Beilstein Handbook Reference)
NSC54752
NSC61281
MFCD00022354
Erl 4206
VINYL CYCLOHEXENE DIOXIDE [HSDB]
3-oxiranyl-7-oxabicyclo[4.1.0]heptane
7-oxa-3-oxiranylbicyclo[4.1.0]heptane
3-Oxiranyl-7-oxabicyclo(4.1.0)heptene
4-VINYLCYCLOHEXENE DIEPOXIDE [IARC]
4-(Epoxyethyl)-7-oxabicyclo[4.1.0]heptane
4-(1,2-Epoxyethyl)-7-oxabicyclo[4.1.0]heptane
Araldite RD 4
Tissonox 206
Araldite DY 032
Bakelite ERL 4206
Unox 206
WLN: T36 BOTJ A- BT3OTJ
Unox EP 206
3-Oxiranyl-7-oxabicyclo[4.1.0]heptene
CAS-106-87-6
4-VINYLCYCLOHEXENE DIEPOXIDE (IARC)
RD 4
EHPE 3158
EHPE 3300
ERRA 4206
3-(oxiran-2-yl)-7-oxabicyclo(4.1.0)heptane
7-Oxabicyclo[4.1.0]heptane, 3-(2-oxiranyl)-
DY032
KRM 2206
4-(oxiran-2-yl)-7-oxabicyclo[4.1.0]heptane
CX 206
EP 206
vinyl cyclohexane diepoxide
3-Oxiranyl- 7-oxabicyclo(4.1.0)heptane
UNII-596C064IG4
1-Epoxyethyl-3,4-epoxy-cyclohexane
4-vinylcyclohexenedioxide
4Vinlycyclohexene dioxide
4Vinylcyclohexene dioxide
Vinylcyclohexane diepoxide
1Vinyl3cyclohexene dioxide
4Vinyl1cyclohexene dioxide
4Vinylcyclohexene diepoxide
Epitope ID:119422
EP-206 (Salt/Mix)
4Vinyl1cyclohexene diepoxide
Vinylcyclohexene dioxide;VCD
MLS001065620
Vinylcyclohexene dioxide, VCD
SCHEMBL106572
1Epoxyethyl3,4epoxycyclohexane
3-EPOXYETHYL-7-OXABICYCLO [4.1.0] HEPTANE
VINYLCYCLOHEXANE DIOXIDE
4Vinyl1,2cyclohexene diepoxide
1Ethyleneoxy3,4epoxycyclohexane
CHEMBL1734307
Unox epoxide 206 (Salt/Mix)
1,2Epoxy4(epoxyethyl)cyclohexane
VINYL CYLCOHEXENE DIEPOXIDE
HMS3039M16
1-Epoxyethyl-3,4-epoxy-cyclohexan
AAA10687
ERL-4206
Cyclohexane, 1,2epoxy4(epoxyethyl)
Tox21_201505
Tox21_300311
3Oxiranyl7oxabicyclo(4.1.0)heptane
BBL011322
STL146309
UCET textile finish 1174 (Obs.)
AKOS005722221
3-EPOXYETHYL-7-OXABICYCLOHEPTANE
7Oxabicyclo(4.1.0)heptane, 3oxiranyl
NCGC00091429-01
NCGC00091429-02
NCGC00091429-03
NCGC00091429-04
NCGC00254198-01
NCGC00259056-01
3(Epoxyethyl)7oxabicyclo(4.1.0)heptane
4(Epoxyethyl)7oxabicyclo(4.1.0)heptane
AS-34998
SMR000568467
SY113814
3-Oxiranyl-7-oxabicyclo(4.1.0) heptane
7Oxabicyclo(4.1.0)heptane, 3(epoxyethyl)
CS-0166800
NS00020724
NS00115895
3(1,2Epoxyethyl)7oxabicyclo(4.1.0)heptane
4(1,2Epoxyethyl)7oxabicyclo(4.1.0)heptane
CYCLOHEXANE,1,2-EPOXY-4(EPOXY ETHYL)
C19311
3-(2-Oxiranyl)-7-oxabicyclo[4.1.0]heptane #
7-oxabicyclo(4.1.0) heptane, 3-(epoxyethyl)-
Q2618250
3-oxiranyl-7-Oxabicyclo[4.1.0]heptane, mixture of isomers
203-437-7
Solubility of 3-(oxiran-2-yl)-7-oxabicyclo[4.1.0]heptane
The solubility of 3-(oxiran-2-yl)-7-oxabicyclo[4.1.0]heptane can be understood by considering several key aspects:
Moreover, it is often helpful to consider the statement: "Like dissolves like." As a rule of thumb, this means:
In summary, while precise solubility data may vary depending on environmental factors and solvent type, 3-(oxiran-2-yl)-7-oxabicyclo[4.1.0]heptane is expected to show enhanced solubility in polar solvents, making it an interesting study case for further solubility investigations.