The chemical substance known as "Phenol, 4-[[[2S]-1-[2-[4-(2-methylpropyl)phenyl]propyl]-4-[4-[[2S]-1-[2-[4-(2-methylpropyl)phenyl]propyl]-2-piperazinyl]butyl]-2-piperazinyl]methyl]-" with CAS number 2066571-97-7 is a complex organic compound characterized by its multi-functional structure. It features a phenolic group, which is indicative of its potential applications in various chemical reactions and as a precursor in the synthesis of other compounds. The presence of piperazine moieties suggests that it may exhibit biological activity, possibly as a pharmaceutical agent or in medicinal chemistry. The branched alkyl groups, specifically the 2-methylpropyl substituents, contribute to its hydrophobic characteristics, influencing solubility and interaction with biological membranes. Overall, this compound's intricate structure may lead to unique properties, making it of interest in research and development within the fields of organic chemistry and pharmacology. However, specific data regarding its physical properties, reactivity, and safety profile would require further investigation and analysis.

Phenol, 4-[[(2S)-1-[2-[4-(2-methylpropyl)phenyl]propyl]-4-[4-[(2S)-1-[2-[4-(2-methylpropyl)phenyl]propyl]-2-piperazinyl]butyl]-2-piperazinyl]methyl]-

2066571-97-7: The chemical substance known as "Phenol, 4-[[[2S]-1-[2-[4-(2-methylpropyl)phenyl]propyl]-4-[4-[[2S]-1-[2-[4-(2-methylpropyl)phenyl]propyl]-2-piperazinyl]butyl]-2-piperazinyl]methyl]-" with CAS number 2066571-97-7 is a complex organic compound characterized by its multi-functional structure. It features a phenolic group, which is indicative of its potential applications in various chemical reactions and as a precursor in the synthesis of other compounds. The presence of piperazine moieties suggests that it may exhibit biological activity, possibly as a pharmaceutical agent or in medicinal chemistry. The branched alkyl groups, specifically the 2-methylpropyl substituents, contribute to its hydrophobic characteristics, influencing solubility and interaction with biological membranes. Overall, this compound's intricate structure may lead to unique properties, making it of interest in research and development within the fields of organic chemistry and pharmacology. However, specific data regarding its physical properties, reactivity, and safety profile would require further investigation and analysis.

<p>PAT-IN-1, a protein acyl transferases (PAT) inhibitor, competitively inhibits Erf2 autopalmitoylation (WO2017011518A1; compound 13) [1].</p>

CAS 2066571-97-7

Phenol, 4-[[(2S)-1-[2-[4-(2-methylpropyl)phenyl]propyl]-4-[4-[(2S)-1-[2-[4-(2-methylpropyl)phenyl]propyl]-2-piperazinyl]butyl]-2-piperazinyl]methyl]-

PAT-IN-1

Ref: TM-T87110