23556-91-4

Basic information

• Product Name: Benzene, 1,1'-[propylidenebis(oxymethylene)]bis-
• CAS NO: 23556-91-4
• Molecular Formula: C17H20O2
• Molecular Weight: 256.345
• Mol File: 23556-91-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, 1,1'-[propylidenebis(oxymethylene)]bis-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,1'-[propylidenebis(oxymethylene)]bis-(23556-91-4)
• EPA Substance Registry System: Benzene, 1,1'-[propylidenebis(oxymethylene)]bis-(23556-91-4)

Safety Data

• Hazardous Substances Data: 23556-91-4(Hazardous Substances Data)

Upstream product

• 123-38-6 propionaldehyde 
• 100-51-6 benzyl alcohol 
• 14593-43-2 benzyl allyl ether 

Downstream Products

• 32426-80-5 (Z)-((prop-1-en-1-yloxy)methyl)benzene 
• 32426-79-2 1-((prop-1-enyloxy)methyl)benzene 
• 140-11-4 Benzyl acetate 
• 122-63-4 benzyl proprionate 
• 15895-87-1 1-((prop-1-enyloxy)methyl)benzene 

Relevant articles and documents

Highly selective isomerization of allyloxyalcohols to cyclic acetals or 1-propenyloxyalcohols

Highly selective isomerization of allyloxyalcohols either to 1-propenyl derivatives or to cyclic acetals of propanal depending on the transition metal (Ru, Rh) complex used is described together with a proposed explanation of an alternative reaction, which permits broad application of the described method.

A selective and convenient ruthenium mediated method for the synthesis of mixed acetals and orthoesters

Addition of alcohols and phenols to O-allyl compounds (allyl ethers and acrolein acetals), catalyzed by [RuCl2(PPh3)3], was examined. Intramolecular addition of an OH group, leading to the formation of cyclic acetals and o