151716-51-7

Basic information

• Product Name: trimethyl-((7R:11R)-trans-phytyl)-benzoquinone-(1.4)
• Synonyms: trimethyl-((7R:11R)-trans-phytyl)-benzoquinone-(1.4)
• CAS NO: 151716-51-7
• Molecular Weight: 428.699
• Mol File: 151716-51-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: trimethyl-((7R:11R)-trans-phytyl)-benzoquinone-(1.4)(CAS DataBase Reference)
• NIST Chemistry Reference: trimethyl-((7R:11R)-trans-phytyl)-benzoquinone-(1.4)(151716-51-7)
• EPA Substance Registry System: trimethyl-((7R:11R)-trans-phytyl)-benzoquinone-(1.4)(151716-51-7)

Safety Data

• Hazardous Substances Data: 151716-51-7(Hazardous Substances Data)

Upstream product

• 700-13-0 Trimethylhydroquinone 
• 150-86-7 phytol 
• 74515-24-5 2.3.5-trimethyl-6-((7R:11R)-trans-phytyl)-hydroquinone 

Relevant articles and documents

Mesoporous and hexagonally ordered CuAl-SBA-15-catalyzed tandem C-C and C-O bond formation between phenols and allylic alcohols

A novel mesoporous catalyst, CuAl-SBA-15, with a hexagonally ordered porous structure prepared via a soft-templating approach in a highly acidic medium is used for tandem C-C and C-O bond formation between phenols and allylic alcohols to afford a variety of dihydrobenzopyrans in good yields. The catalyst is also found to be highly active for the synthesis of vitamin E and can be recycled several times without significant loss of its activity.

929. Chrom-3-en-6-ols. The action of pyridine on alk-2-enyl-benzoquinones

Allylbenzoquinones are converted by treatment with pyridine into quinols and chrom-3-en-6-ols. The tendency for the latter reaction to occur increases as the benzoquinone ring becomes more highly substituted.