CAS 81518-74-3

Benzene, [(4-pentenyloxy)methyl]-

Description:

Benzene, [(4-pentenyloxy)methyl]- is an organic compound characterized by its benzene ring structure substituted with a 4-pentenyloxy methyl group. This compound features a hydrophobic aromatic ring, which contributes to its stability and unique chemical properties. The presence of the pentenyloxy group introduces a degree of reactivity due to the unsaturation in the pentene chain, allowing for potential participation in various chemical reactions, such as polymerization or addition reactions. The compound is likely to be a colorless to pale yellow liquid with a characteristic aromatic odor. Its solubility in organic solvents, combined with its hydrophobic nature, makes it suitable for applications in organic synthesis and as an intermediate in the production of more complex molecules. Safety considerations are important, as compounds containing benzene rings can be toxic and potentially carcinogenic, necessitating proper handling and storage protocols. Overall, this compound exemplifies the diverse reactivity and utility of substituted benzene derivatives in organic chemistry.

Formula: C₁₂H₁₆O

[(Pent-4-en-1-yloxy)methyl]benzene

CAS: 81518-74-3

[(Pent-4-en-1-yloxy)methyl]benzene

Purity: 95% +(stabilized with TBC)

Molecular weight: 176.26g/mol

Ref: 54-OR1065758

[(Pent-4-en-1-yloxy)methyl]benzene

CAS: 81518-74-3

[(Pent-4-en-1-yloxy)methyl]benzene is an ester that is used in the synthesis of other compounds. It is produced by the catalytic cleavage of sulfoxides and interacts with a variety of ligands. [(Pent-4-en-1-yloxy)methyl]benzene can be used as a precursor to allylic esters, which are important in organic synthesis because they are often more reactive than their parent olefin. It has been shown to undergo allylic oxidation and allylic esters, which are important reactions in organic chemistry. Allylic oxidation involves the addition of oxygen to an unsaturated carbon atom, while allylic esters involve the addition of an alcohol to an unsaturated carbon atom. This functionalization process is useful for making molecules that contain two different types of functional groups.

Formula: C₁₂H₁₆O

Purity: Min. 95%

Molecular weight: 176.25 g/mol

Ref: 3D-GDA51874