CAS 22388-89-2

2H-Pyran-2-one,6-[(1E,3E)-1,3-dimethyl-4-(4-nitrophenyl)-1,3-butadien-1-yl]-4-methoxy-3-methyl-

Description:

2H-Pyran-2-one, 6-[(1E,3E)-1,3-dimethyl-4-(4-nitrophenyl)-1,3-butadien-1-yl]-4-methoxy-3-methyl- is an organic compound characterized by its complex structure, which includes a pyranone ring and a substituted butadiene moiety. The presence of a methoxy group and a nitrophenyl group contributes to its chemical reactivity and potential applications in various fields, including pharmaceuticals and materials science. This compound is likely to exhibit properties typical of conjugated systems, such as UV-Vis absorbance due to the extended π-electron system. Its molecular structure suggests potential for biological activity, possibly as a dye or in medicinal chemistry, although specific biological properties would require empirical investigation. The CAS number 22388-89-2 uniquely identifies this compound in chemical databases, facilitating research and regulatory compliance. Overall, the compound's unique functional groups and structural features make it of interest for further study in synthetic and applied chemistry.

Formula: C₁₉H₁₉NO₅

Synonyms:

• 2H-Pyran-2-one,6-[(1E,3E)-1,3-dimethyl-4-(4-nitrophenyl)-1,3-butadienyl]-4-methoxy-3-methyl-(9CI)
• 2H-Pyran-2-one,6-[1,3-dimethyl-4-(4-nitrophenyl)-1,3-butadienyl]-4-methoxy-3-methyl-, (E,E)-
• 2H-Pyran-2-one,6-[1,3-dimethyl-4-(p-nitrophenyl)-1,3-butadienyl]-4-methoxy-3-methyl- (8CI)
• Griseulin
• Luteoreticulin

Luteoreticulin

CAS: 22388-89-2

Luteoreticulin, a nitro-containing bacterial metabolite first isolated from S. luteoreticuli, exhibits mosquitocidal activity against A. aegypti at a concentration of 6.25 mg/L and nematocidal activity against C. elegans.

Formula: C₁₉H₁₉NO₅

Color and Shape: Solid

Molecular weight: 341.36

Ref: TM-TN7552

Luteoreticulin

CAS: 22388-89-2

Ref: 7W-GW6055