Interesting facts
Interesting Facts about 1-Vinyloxybutane
1-Vinyloxybutane, a versatile compound in organic chemistry, is primarily utilized as an intermediary in the synthesis of various chemicals. Here are some engaging insights into this fascinating compound:
- Functional Group: This compound features a vinyl (-C=C-) group, which lends it unique reactivity and the ability to participate in various polymerization reactions, making it a valuable precursor in materials science.
- Synthesis Potential: The presence of both an ether and vinyl functional group allows 1-vinyloxybutane to serve as a building block for complex molecules, including various pharmaceuticals. Its synthesis can typically be achieved through hydrolysis reactions or via alkylation methods.
- Applications in Research: In synthetic organic chemistry, this compound plays a crucial role in the development of new polymers and copolymers. It is often explored for its potential in producing biocompatible materials.
- Reactivity: The vinyl group makes it reactive towards electrophiles, thus opening pathways for various addition reactions. This property is essential for designing targeted modifications in organic synthesis processes.
- Environmental Impact: As with many organic compounds, the implications of 1-vinyloxybutane for environmental sustainability are a key focus. Studying its breakdown processes and potential for biodegradation is vital in the context of eco-friendly chemistry.
Overall, 1-vinyloxybutane stands out as a compound with significant potential in both industrial applications and academic research, symbolizing the beauty and complexity of organic reactions.
Synonyms
BUTYL VINYL ETHER
n-Butyl vinyl ether
111-34-2
Vinyl butyl ether
1-(Ethenyloxy)butane
Butane, 1-(ethenyloxy)-
Butoxyethylene
Butoxyethene
Ether, butyl vinyl
1-ethenoxybutane
1-(vinyloxy)butane
Vinyl n-butyl ether
Ethenyl n-butyl ether
n-butylvinylether
1-vinyloxybutane
NSC 8264
n-butylvinyl ether
Butyl vinyl ether, inhibited
BVE
DTXSID5051575
NSC-8264
321YRT7173
Agrisynth BVE
Butil vinil eter
Butil vinil eter [Spanish]
25232-87-5
Ether butylvinylique
Ether butylvinylique [French]
HSDB 6384
n-Butyl Vinyl Ether (Stabilized with 0.01% KOH)
EINECS 203-860-7
UN2352
BRN 1560217
butylvinylether
Vinilin
Vinipol
Butoxy-ethene
butyl vinylether
butylvinyl ether
AI3-24225
UNII-321YRT7173
butyl-vinyl ether
n-butyl vinylether
1-vinyloxy-butane
Shostakovski balsam
Vinipol vb 2
vinyl-1-butylether
vinyl-n-butyl ether
1-Butoxyethylene #
MFCD00009454
1-(Vinyloxy)-butane
1-(ethenyloxy)-butane
1-BUTOXYETHENE
n-C4H9OCH=CH2
EC 203-860-7
SCHEMBL19482
4-01-00-02052 (Beilstein Handbook Reference)
UN 2352 (Salt/Mix)
Shostakovsky balsam (Salt/Mix)
WLN: 4O1U1
CHEMBL3561125
DTXCID9030127
BUTYL VINYL ETHER [HSDB]
NSC8264
CS-Z0017
Tox21_303721
STL283942
AKOS009031191
Butyl vinyl ether, analytical standard
AT27752
NCGC00357033-01
CAS-111-34-2
FB166126
B0746
NS00006709
EN300-21299
A802345
Q1018214
BUTYL VINYL ETHER (STABILIZED WITH TRIHEXYLAMINE)
F0001-0239
n-Butyl Vinyl Ether (Stabilized with 0.01per cent KOH)
Butyl vinyl ether, inhibited [UN2352] [Flammable liquid]
InChI=1/C6H12O/c1-3-5-6-7-4-2/h4H,2-3,5-6H2,1H
Butyl vinyl ether, 98% contains 0.01% potassium hydroxide as stabilizer
Butyl vinyl ether, contains 0.01% potassium hydroxide as stabilizer, 98%
Solubility of 1-Vinyloxybutane
1-Vinyloxybutane, known for its unique structure, displays interesting solubility characteristics. Being an ether, it possesses a hydrophobic hydrocarbon component paired with a polar ether linkage, affecting its ability to dissolve in various solvents.
Solubility Characteristics:
Due to these properties, it is often essential to consider the solvent selection based on the desired application involving 1-vinyloxybutane. In conclusion, while it shows limited solubility in water, its compatibility with organic solvents underscores its versatility in chemical processes.