256487-37-3

Basic information

• Product Name: 2-[2-(1,3-Dimethyl-2-methylene-cyclohexyl)-ethyl]-2,5,5-trimethyl-[1,3]dioxane
• Synonyms: 2-[2-(1,3-Dimethyl-2-methylene-cyclohexyl)-ethyl]-2,5,5-trimethyl-[1,3]dioxane
• CAS NO: 256487-37-3
• Molecular Weight: 280.451
• Mol File: 256487-37-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-[2-(1,3-Dimethyl-2-methylene-cyclohexyl)-ethyl]-2,5,5-trimethyl-[1,3]dioxane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[2-(1,3-Dimethyl-2-methylene-cyclohexyl)-ethyl]-2,5,5-trimethyl-[1,3]dioxane(256487-37-3)
• EPA Substance Registry System: 2-[2-(1,3-Dimethyl-2-methylene-cyclohexyl)-ethyl]-2,5,5-trimethyl-[1,3]dioxane(256487-37-3)

Safety Data

• Hazardous Substances Data: 256487-37-3(Hazardous Substances Data)

Upstream product

• 1779-49-3 Methyltriphenylphosphonium bromide 
• 256487-36-2 2,6-Dimethyl-2-[2-(2,5,5-trimethyl-[1,3]dioxan-2-yl)-ethyl]-cyclohexanone 
• 2816-57-1 2,6-dimethylcyclohexanone 
• 4071-74-3 2,6-dimethyl-2-(3-oxobutyl)cyclohexanone 
• 126-30-7 2,2-Dimethyl-1,3-propanediol 
• 63547-53-5 2,6-dimethyl-1-(trimethylsiloxy)cyclohexene 

Relevant articles and documents

A Total Synthesis of the Sesquiterpene Quinone Metachromin-A

The first total synthesis of the marine natural product metachromin A was accomplished through a convergent synthesis amenable to the preparation of synthetic analogues.The main features of this synthesis are the introduction the oxygenation at C17 employing a Thiele acetoxylation reaction and a stereoselective Horner-Wadsworth-Emmons coupling of a nonstabilized phosphonate with a methyl ketone derivative to generate the required (E)-trisubstituted double bond.