CAS 7315-32-4
:5-ethenyl-1,3-benzodioxole
Description:
5-Ethenyl-1,3-benzodioxole, also known as 5-vinyl-1,3-benzodioxole, is an organic compound characterized by its unique bicyclic structure that incorporates a dioxole ring fused to a benzene ring. This compound features a vinyl group (-CH=CH2) at the 5-position of the benzodioxole, which contributes to its reactivity and potential applications in polymer chemistry and organic synthesis. It is typically a colorless to pale yellow liquid with a distinctive aromatic odor. The presence of the vinyl group allows for participation in various addition reactions, making it useful in the production of polymers and other derivatives. Additionally, the compound may exhibit interesting electronic properties due to the conjugated system formed by the vinyl and aromatic components. Its solubility in organic solvents and relatively low boiling point make it suitable for various chemical processes. However, safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested.
Formula:C9H8O2
InChI:InChI=1/C9H8O2/c1-2-7-3-4-8-9(5-7)11-6-10-8/h2-5H,1,6H2
SMILES:C=Cc1ccc2c(c1)OCO2
Synonyms:- 1,3-Benzodioxole, 5-ethenyl-
- 5-Ethenylbenzo[1,3]Dioxole
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Found 5 products.
5-VINYLBENZO[D][1,3]DIOXOLE
CAS:Formula:C9H8O2Purity:95%Color and Shape:LiquidMolecular weight:148.15865-Vinylbenzo[d][1,3]dioxole
CAS:5-Vinylbenzo[d][1,3]dioxolePurity:95% (stabilized with TBC)Molecular weight:148.16g/mol5-Vinyl-1,3-benzodioxole
CAS:Formula:C9H8O2Purity:>95.0%(GC)Color and Shape:Colorless to Yellow clear liquidMolecular weight:148.165-Vinylbenzo[d][1,3]dioxole (stabilized with TBC)
CAS:Controlled Product<p>Stability Light Sensitive<br>Applications 5-Vinylbenzo[d][1,3]dioxole (cas# 7315-32-4) is a useful research chemical.<br></p>Formula:C9H8O2Color and Shape:NeatMolecular weight:148.165-Vinylbenzo[d][1,3]dioxole
CAS:Controlled Product<p>5-Vinylbenzo[d][1,3]dioxole is an organic compound that belongs to the amide class. It has been shown to be a potent inhibitor of leishmania and related protozoan parasites. 5-Vinylbenzo[d][1,3]dioxole inhibits these parasites by targeting the amine group on their surface, which is responsible for the conversion of ammonium nitrate into nitric oxide. 5-Vinylbenzo[d][1,3]dioxole also has reactive properties and can form covalent bonds with other molecules in a process called redox chemistry. This property makes it useful as a reactive intermediate in chemical synthesis. 5-Vinylbenzo[d][1,3]dioxole is an example of a primary amino compound because it does not contain any secondary or tertiary amines.</p>Formula:C9H8O2Purity:Min. 95%Molecular weight:148.16 g/mol





