Interesting facts
Interesting Facts about 2-[4-(oxiran-2-yl)butyl]oxirane
2-[4-(oxiran-2-yl)butyl]oxirane, commonly referred to as a type of epoxide, has intriguing applications and properties that make it notable in the field of chemistry. Here are some fascinating insights:
- Epoxide Structure: This compound contains a three-membered cyclic ether known as an epoxide, which is known for its reactivity. The strained ring structure makes epoxides highly reactive, allowing them to participate in various chemical reactions, such as ring-opening mechanisms.
- Applications: Epoxides like this compound are key intermediates in the synthesis of various pharmaceuticals, agrochemicals, and polymer materials. Their unique reactivity allows them to be used in the manufacture of coatings, adhesives, and composite materials.
- Biological Significance: The reactivity of 2-[4-(oxiran-2-yl)butyl]oxirane also lends itself to being studied for its potential biological effects, including interactions with biological macromolecules. This characteristic is critical in drug design, where the ability to form covalent bonds with biomolecules can influence therapeutic outcomes.
- Synthetic Utility: Chemists often utilize this compound as a building block in synthetic organic chemistry. Through strategic functionalization, it can lead to the formation of complex molecules with desired properties.
- Regioselectivity in Reactions: The presence of the oxirane ring offers interesting opportunities for regioselectivity in chemical reactions. Understanding how this compound reacts can help chemists to predict outcomes and optimize conditions for desired transformations.
In conclusion, 2-[4-(oxiran-2-yl)butyl]oxirane stands as a testament to the intricate balance of structure and reactivity in organic compounds. Its applications span across various fields, showcasing the depth and versatility of epoxide chemistry.
Synonyms
1,2,7,8-DIEPOXYOCTANE
2426-07-5
1,2:7,8-Diepoxyoctane
1,7-Octadiene diepoxide
Oxirane, 2,2'-(1,4-butanediyl)bis-
Octane, 1,2:7,8-diepoxy-
4IJ1M5W7LL
CCRIS 963
2,2'-butane-1,4-diyldioxirane
EINECS 219-375-9
UNII-4IJ1M5W7LL
NSC 269058
NSC-269058
BRN 0104873
AI3-52822
CHEBI:23705
DTXSID00862928
2,2'-TETRAMETHYLENEBISOXIRANE
J2.154G
2,2'-(1,4-BUTANEDIYL)BIS(OXIRANE)
5-19-01-00229 (Beilstein Handbook Reference)
DTXCID90811627
Oxirane, 2,2'-(1,4-butanediyl)bis-(9CI)
lfklpjrvshjzpl-uhfffaoysa-n
1,4-Di(oxiran-2-yl)butane
1,2-Epoxy-7,8-epoxyoctane
2-[4-(oxiran-2-yl)butyl]oxirane
2,2'-(1,4-Butanediyl)bisoxirane
MFCD00005155
2-(4-oxiran-2-ylbutyl)oxirane
1,8-epoxyoctane
1,8-Diepoxyoctane
Octane,2:7,8-diepoxy-
SCHEMBL33715
WLN: T3OTJ B4- BT3OTJ
1,2,7,8-Diepoxyoctane, 97%
BCP21857
Oxirane,2'-(1,4-butanediyl)bis-
GEO-01029
NSC269058
2-[4-(2-Oxiranyl)butyl]oxirane #
AKOS015999611
FO75919
CS-11846
SY031422
CS-0313243
D1586
NS00047370
F10176
Q27109807
1,4-Buthylenebis(oxirane);1,7-Octadiene diepoxide;Oxirane, 2,2'-(1,4-butanediyl)bis-
Solubility of 2-[4-(oxiran-2-yl)butyl]oxirane
The solubility of 2-[4-(oxiran-2-yl)butyl]oxirane, also known as a glycidyl derivative, can be influenced by several factors. This compound, with its oxirane functionality, exhibits interesting solubility characteristics that are worth noting:
In practical terms, it is essential to determine the solubility in various solvents to understand the behavior of 2-[4-(oxiran-2-yl)butyl]oxirane in applications. As is often said in chemistry, "solubility is the key to reactivity," making it vital to explore this property when considering this compound's usage in various formulations and reactions.