714956-91-9

Basic information

• Product Name: (2E,6E)-8-(2,5-Bis-benzyloxy-phenyl)-2,6-dimethyl-octa-2,6-dien-1-ol
• Synonyms: (2E,6E)-8-(2,5-Bis-benzyloxy-phenyl)-2,6-dimethyl-octa-2,6-dien-1-ol
• CAS NO: 714956-91-9
• Molecular Weight: 442.598
• Mol File: 714956-91-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2E,6E)-8-(2,5-Bis-benzyloxy-phenyl)-2,6-dimethyl-octa-2,6-dien-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (2E,6E)-8-(2,5-Bis-benzyloxy-phenyl)-2,6-dimethyl-octa-2,6-dien-1-ol(714956-91-9)
• EPA Substance Registry System: (2E,6E)-8-(2,5-Bis-benzyloxy-phenyl)-2,6-dimethyl-octa-2,6-dien-1-ol(714956-91-9)

Safety Data

• Hazardous Substances Data: 714956-91-9(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 10457-66-6 (E)-2-(3,7-dimethylocta-2,6-dienyl)benzene-1,4-diol 
• 714956-90-8 1,4-Bis-benzyloxy-2-((E)-3,7-dimethyl-octa-2,6-dienyl)-benzene 

Downstream Products

• 714956-89-5 1,4-Bis-benzyloxy-2-[(2E,6E)-3,7-dimethyl-9-(2,6,6-trimethyl-cyclohex-1-enyl)-nona-2,6-dienyl]-benzene 
• 714956-92-0 1,4-Bis-benzyloxy-2-((2E,6E)-8-chloro-3,7-dimethyl-octa-2,6-dienyl)-benzene 

Relevant articles and documents

Synthesis of jaspaquinol and effect on viability of normal and malignant bladder epithelial cell lines

The synthesis of jaspaquinol 1, a monocyclic diterpene-benzenoid, is reported. Two synthetic routes to this natural product have been developed. The first, utilises a difunctional terpene derivative containing different leaving groups, facilitating the selective introduction of the cyclohexenyl and benzenoid fragments. The alternative route employs a regiospecific Stille cross-coupling reaction to introduce the cyclohexenyl fragment, which occurs without allylic transposition. Preliminary data shows the cell viability of 1 against normal and malignant human bladder epithelial cell lines.