The chemical substance known as 2,6,10,14,18,22,26,30,34,38,42-Tetratetracontaundecaen-1-ol,3,7,11,15,19,23,27,31,35,39,43-undecamethyl-, with the CAS number 26296-50-4, is a complex organic compound characterized by a long hydrocarbon chain and multiple double bonds. This compound belongs to the class of alcohols, specifically a polyunsaturated alcohol, due to the presence of hydroxyl (-OH) functional groups and multiple cis and trans double bonds within its structure. The extensive carbon chain contributes to its hydrophobic nature, making it less soluble in water but more soluble in organic solvents. The presence of multiple double bonds indicates that it may exhibit unique reactivity patterns, including potential for oxidation. Additionally, the specific stereochemistry (cis and trans configurations) of the double bonds can influence its physical properties, such as melting and boiling points, as well as its biological activity. Overall, this compound's structure suggests potential applications in various fields, including materials science and biochemistry, although specific applications would depend on further research and characterization.

2,6,10,14,18,22,26,30,34,38,42-Tetratetracontaundecaen-1-ol,3,7,11,15,19,23,27,31,35,39,43-undecamethyl-,(2Z,6Z,10Z,14Z,18Z,22Z,26Z,30E,34E,38E)-

26296-50-4: The chemical substance known as 2,6,10,14,18,22,26,30,34,38,42-Tetratetracontaundecaen-1-ol,3,7,11,15,19,23,27,31,35,39,43-undecamethyl-, with the CAS number 26296-50-4, is a complex organic compound characterized by a long hydrocarbon chain and multiple double bonds. This compound belongs to the class of alcohols, specifically a polyunsaturated alcohol, due to the presence of hydroxyl (-OH) functional groups and multiple cis and trans double bonds within its structure. The extensive carbon chain contributes to its hydrophobic nature, making it less soluble in water but more soluble in organic solvents. The presence of multiple double bonds indicates that it may exhibit unique reactivity patterns, including potential for oxidation. Additionally, the specific stereochemistry (cis and trans configurations) of the double bonds can influence its physical properties, such as melting and boiling points, as well as its biological activity. Overall, this compound's structure suggests potential applications in various fields, including materials science and biochemistry, although specific applications would depend on further research and characterization.

Ficaprenol 11 is a natural product of Artocarpus, Moraceae.

CAS 26296-50-4

2,6,10,14,18,22,26,30,34,38,42-Tetratetracontaundecaen-1-ol,3,7,11,15,19,23,27,31,35,39,43-undecamethyl-,(2Z,6Z,10Z,14Z,18Z,22Z,26Z,30E,34E,38E)-

Ficaprenol 11

Ref: TM-TN4056

Ficaprenol 11

Ref: BP-SBP01859