79370-71-1

Basic information

• Product Name: (2E,6E,10E,14E,18E,22E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene-1-ol
• Synonyms: (2E,6E,10E,14E,18E,22E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene-1-ol
• CAS NO: 79370-71-1
• Molecular Weight: 426.726
• Mol File: 79370-71-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2E,6E,10E,14E,18E,22E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (2E,6E,10E,14E,18E,22E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene-1-ol(79370-71-1)
• EPA Substance Registry System: (2E,6E,10E,14E,18E,22E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene-1-ol(79370-71-1)

Safety Data

• Hazardous Substances Data: 79370-71-1(Hazardous Substances Data)

Upstream product

• 111-02-4 2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene 

Relevant articles and documents

Solid-phase selenium-catalyzed selective allylic chlorination of polyprenoids: Facile syntheses of biologically active terpenoids

Regioselective halogenation of the terminal isopropylidene unit of different acyclic polyolefinic polyprenoids (farnesyl acetate, geranylgeranyl acetate, squalene, etc.) using NCS/catalytic polymer-supported selenenyl bromide is described; good to excellent yields are obtained (68-96%). The first applications of this protocol include the concise synthesis of bioactive terpenoids 1-3.