100058-51-3

Basic information

• Product Name: (1-(allyloxy)-4-ethoxybenzene)
• Synonyms: (1-(allyloxy)-4-ethoxybenzene)
• CAS NO: 100058-51-3
• Molecular Weight: 178.231
• Mol File: 100058-51-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (1-(allyloxy)-4-ethoxybenzene)(CAS DataBase Reference)
• NIST Chemistry Reference: (1-(allyloxy)-4-ethoxybenzene)(100058-51-3)
• EPA Substance Registry System: (1-(allyloxy)-4-ethoxybenzene)(100058-51-3)

Safety Data

• Hazardous Substances Data: 100058-51-3(Hazardous Substances Data)

Upstream product

• 622-62-8 4-Ethoxyphenol 
• 106-95-6 allyl bromide 

Downstream Products

• 857627-97-5 1-acetoxy-4-ethoxy-2-allyl-benzene 
• 142875-24-9 2-allyl-4-ethoxyphenol 

Relevant articles and documents

Synthesis and some features of phase behavior of chiral p-alkoxyphenyl glycerol ethers

A series of (S)-3-(4-alkoxyphenoxy)propane-1,2-diols was prepared with the enantiomeric excess 86-92% by Sharpless asymmetric dihydroxylation of 1-alkoxy-4-allyloxybenzenes with an AD-mix-β mixture. R-Enantiomers with enantiomeric excess 97-99% and racemic samples were obtained by reaction of sodium p-substituted phenolates with (R)- and rac-3-chloropropane-1,2-diol. The phase behavior of racemates and scalemates in the produced homolog series of glycerol aryl ethers with hydrocarbon substituents of various length was examined by means of thermomicroscopy. The higher memberes of the homolog series of both racemic and scalemic diols undergo at heating an enantiotropic phase transition to a smectic liquid crystal phase.

METHODS AND COMPOSITIONS FOR CONTROL OF CABBAGE LOOPER, Trichoplusia ni

The invention provides in part dialkoxybenzene compounds for controlling infestation by a Trichoplusia ni, and methods thereof. The compounds include a compound of Formula I: where R1 may be methyl, ethyl, propyl, n-butyl, isopentyl(3-methylbutyl) or allyl; R2 may be at positions 2, 3 or 4 and may be H, methyl, ethyl, propyl, n-butyl, isopentyl(3-methylbutyl) or allyl; and R3 may be optionally present at positions 2, 3 and 4, and is allyl; except that when R2 is at position 2, R3 if present is at position 3, and when R2 is at position 3, R3 if present is at positions 2 or 4, and when R2 is at position 4, R3 if present is at position 2, and when R2 is at position 4 and R3, if present, has reacted with an OH group at position 1 in a Markovnikov sense, then R3 becomes R4, a dihydrofuran.