Skip to main content

2-Vinyloxirane

ADVERTISEMENT
Identification
Molecular formula
C5H8O
CAS number
106-86-5
IUPAC name
2-vinyloxirane
State
State

At room temperature, 2-Vinyloxirane is found in a liquid state.

Melting point (Celsius)
-102.00
Melting point (Kelvin)
171.15
Boiling point (Celsius)
88.00
Boiling point (Kelvin)
361.15
General information
Molecular weight
70.12g/mol
Molar mass
70.0900g/mol
Density
0.9018g/cm3
Appearence

2-Vinyloxirane is a colorless liquid with a mild characteristic odor.

Comment on solubility

Solubility of 2-vinyloxirane

2-vinyloxirane, also known as vinyl-oxide, exhibits specific solubility characteristics that are important to consider in various chemical contexts. This compound is generally soluble in organic solvents and can demonstrate variable solubility when interacting with polar and non-polar substances. Here are some notable points regarding its solubility:

  • Polar solvents: 2-vinyloxirane tends to have limited solubility in water due to the hydrophobic residues present in its structure.
  • Non-polar solvents: It is more soluble in non-polar solvents like hexane or ether, owing to the similarity in the intermolecular forces between the solvent and the solute.
  • Reactivity: The presence of the epoxide ring may influence solubility as it can participate in reactions with nucleophiles, potentially leading to solubility changes in various environments.

In summary, the solubility of 2-vinyloxirane is primarily dictated by the nature of the solvent and the compound's chemical structure. As the saying goes, "like dissolves like," and this principle aptly applies to understanding the solubility behaviors of this epoxide compound.

Interesting facts

Interesting Facts About 2-Vinyloxirane

2-Vinyloxirane, also known as 2-vinyloxirane or vinyl oxirane, is a fascinating compound in the field of organic chemistry. This compound stands out due to its unique structural and functional properties, making it an important subject of study.

Key Characteristics:

  • Reactive Epoxide: As an epoxide, 2-vinyloxirane features a three-membered cyclic ether. This structure gives it a high degree of reactivity, particularly in nucleophilic substitution reactions.
  • Versatile Building Block: It serves as a crucial intermediate in the synthesis of various chemical compounds, including pharmaceuticals and polymers.
  • Vinyl Group Influence: The presence of the vinyl group enhances its reactivity, allowing for the formation of diverse derivatives when subjected to different chemical reactions.

Applications:

2-Vinyloxirane has multiple applications across different fields. Here are a few notable examples:

  • Synthetic Chemistry: It is used in the production of polymers through copolymerization processes.
  • Pharmaceuticals: The compound is being explored for its potential in developing novel drug molecules.

A Final Thought:

The ability of 2-vinyloxirane to participate in various chemical reactions while acting as a precursor to valuable materials demonstrates its significance in organic synthesis. As one researcher aptly noted, “The chemistry of epoxides like 2-vinyloxirane expands the toolkit of synthetic chemists, paving the way for innovative advancements.” Such characteristics underscore the importance of studying this intriguing compound in the quest for new and efficient chemical processes.

Synonyms
Butadiene monoxide
3,4-EPOXY-1-BUTENE
1,2-Epoxy-3-butene
Butadiene epoxide
Vinyloxirane
Oxirane, 2-ethenyl-
1,2-Epoxybutene
3,4-Epoxybut-1-ene
Monoepoxybutene
Monoepoxybutadiene
vinyl oxirane
CCRIS 2614
HSDB 5520
UNII-478ERR5NKR
EINECS 213-210-4
478ERR5NKR
DTXSID4025240
3,4-Epoxybutene-1
AI3-16049
NSC-8023
1,2-Epoxy-3-butylene
NSC-24251
DTXCID105240
3,4-EPOXY-1-BUTENE [HSDB]
butadienemonoepoxide
Oxirane, ethenyl
1,2Epoxybutene
3,4Epoxybutene
1,2Epoxy3butene
1,2Epoxybutene3
1,2Oxido3butene
3,4Epoxybut1ene
Oxirane, 2ethenyl
1,2-EB
1,3Butadiene oxide
1Butene, 3,4epoxy
(+-)-VINYLOXIRANE
BUTENE 3,4-EPOXIDE
(.+-.)-VINYLOXIRANE
1-BUTENE,3,4-EPOXY-
epoxybutene
gxbyfvgcmpjvjx-uhfffaoysa-n
un1993
930-22-3
2-Vinyloxirane
2-ethenyloxirane
Oxirane, ethenyl-
Butadiene monooxide
Butadiene oxide
Butadiene monoepoxide
Ethenyloxirane
Vinylethylene oxide
1,2-Epoxybutene-3
1,2-Oxido-3-butene
1,3-Butadiene monoepoxide
1,3-Butadiene oxide
1-Butene, 3,4-epoxy-
3,4-Epoxybutene
NSC 8023
NSC 24251
1,3-Butadiene monooxide
(+/-)-VINYLOXIRANE
MFCD00005149
1-Butene,4-epoxy-
WLN: T3OTJ B1U1
26703-03-7
2-Vinyloxirane #
VINYL EPOXIDE
1,2-epoxybut-3-ene
3,4-epoxy-butene-1
1,3-butadiene monoxide
CHEMBL1299388
3,4-Epoxy-1-butene, 98%
NSC8023
NSC24251
Tox21_200871
BBL102661
STL556465
AKOS005257726
FE03375
NCGC00091691-01
NCGC00091691-02
NCGC00258425-01
CAS-930-22-3
DB-073082
DB-073083
(Oxiran-2-yl)ethylene; 1,2-Epoxybutene-3
E0337
NS00039515
NS00115902
EN300-98979
D90487
Q15910431