The chemical substance known as "3-[(E)-4-Acetoxy-5-(1,2,6-trimethyl-3-oxocyclohexyl)-3-methyl-2-pentenyl]-5-chloro-2,4-dihydroxy-6-methylbenzaldehyde" with CAS number 38965-84-3 is a complex organic compound characterized by its multi-functional groups and structural features. It contains a benzaldehyde moiety, which is indicative of its potential reactivity and applications in organic synthesis. The presence of hydroxyl groups suggests that it may exhibit hydrogen bonding capabilities, influencing its solubility and interaction with other molecules. The acetoxy group contributes to its reactivity, potentially allowing for esterification or other chemical transformations. The compound's structure includes a cyclohexyl ring, which may impart steric effects and influence its biological activity. Additionally, the presence of multiple methyl groups can enhance lipophilicity, affecting its distribution in biological systems. Overall, this compound's unique structural characteristics may render it of interest in medicinal chemistry, particularly in the development of pharmaceuticals or agrochemicals.

3-[(E)-4-Acetoxy-5-(1,2,6-trimethyl-3-oxocyclohexyl)-3-methyl-2-pentenyl]-5-chloro-2,4-dihydroxy-6-methylbenzaldehyde

38965-84-3: The chemical substance known as "3-[(E)-4-Acetoxy-5-(1,2,6-trimethyl-3-oxocyclohexyl)-3-methyl-2-pentenyl]-5-chloro-2,4-dihydroxy-6-methylbenzaldehyde" with CAS number 38965-84-3 is a complex organic compound characterized by its multi-functional groups and structural features. It contains a benzaldehyde moiety, which is indicative of its potential reactivity and applications in organic synthesis. The presence of hydroxyl groups suggests that it may exhibit hydrogen bonding capabilities, influencing its solubility and interaction with other molecules. The acetoxy group contributes to its reactivity, potentially allowing for esterification or other chemical transformations. The compound's structure includes a cyclohexyl ring, which may impart steric effects and influence its biological activity. Additionally, the presence of multiple methyl groups can enhance lipophilicity, affecting its distribution in biological systems. Overall, this compound's unique structural characteristics may render it of interest in medicinal chemistry, particularly in the development of pharmaceuticals or agrochemicals.

<p>Chloronectrin exhibits activity against Gram-positive bacteria.</p>

CAS 38965-84-3

3-[(E)-4-Acetoxy-5-(1,2,6-trimethyl-3-oxocyclohexyl)-3-methyl-2-pentenyl]-5-chloro-2,4-dihydroxy-6-methylbenzaldehyde

Chloronectrin

Ref: TM-TN9845