698-91-9

Basic information

• Product Name: Benzene, [(1-methylethenyl)oxy]-
• CAS NO: 698-91-9
• Molecular Formula: C9H10O
• Molecular Weight: 134.178
• Mol File: 698-91-9.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzene, [(1-methylethenyl)oxy]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [(1-methylethenyl)oxy]-(698-91-9)
• EPA Substance Registry System: Benzene, [(1-methylethenyl)oxy]-(698-91-9)

Safety Data

• Hazardous Substances Data: 698-91-9(Hazardous Substances Data)

Upstream product

• 78-75-1 1,2-Dibromopropane 
• 139-02-6 sodium phenoxide 
• 90561-10-7 (2-bromopropoxy)benzene 
• 86623-33-8 (β-bromo-isopropyl)-phenyl ether 
• 74-99-7 prop-1-yne 
• 108-95-2 phenol 
• 75-24-1 trimethylaluminum 
• 122-79-2 Phenyl acetate 
• 17333-73-2 phenylium 
• 75-56-9 methyloxirane 
• 7732-18-5 water 
• 463-49-0 1,2-propanediene 
• 57422-37-4 3-phenoxy-crotonic acid ethyl ester 
• 857335-90-1 1-iodo-2-isopropoxybenzene 

Downstream Products

• 10277-93-7 2-isopropenylphenol 
• 98995-25-6 (α-chloro-isopropyl)-phenyl ether 
• 100975-82-4 acetone-diphenylacetal 
• 144866-82-0 (2R,3E)-(+)-<2-(2'-phenoxy-isopropyl)oxy>pentenenitrile 
• 926-66-9 2-ethoxyprop-1-ene 
• 126-84-1 2,2-diethoxypropane 
• 108-95-2 phenol 
• 144866-83-1 (2R,3E)-(-)-1-methylamino-2-(2'-phenoxy-isopropyl)oxypentene 
• 81634-59-5 2-methyl-2-phenoxybutane 
• 100519-82-2 (1,1-dimethyl-butyl)-phenyl ether 
• 88-69-7 2-(1-methylethyl)phenol 
• 5026-12-0 2-(2-hydroxyphenyl)-2,4,4-trimethylchroman 
• 144330-59-6 pentacarbonyl{(phenyl)(methyl)(phenyloxy)1,2-diselenolane}tungsten 

Relevant articles and documents

Catalytic dehydrogenation of o-alkylated or o-alkoxylated iodoarenes with concomitant hydrogenolysis

Palladium-catalyzed dehydrogenation of suitable chains bonded to an ortho position of an iodoarene has been achieved by two methods both involving oxidative addition of the iodoarene to palladium(0) and palladacycle formation under mild conditions.

2-Phenoxypropene as protective reagent of chiral alcohols

2-Phenoxypropene (2) was applied as a novel protective reagent of chiral alcohols, yielding 2-phenoxy-isopropyl (PIP) ethers. Introduction and cleavage of the protective group was achieved under mild conditions.

DECOMPOSITION HETEROLITIQUE DE PERCARBONATES DE O,O-METHYL-1 PHENYL-1 ETHYLE ET O-ALKYLE OU O-VINYLE EN SOLUTION

O,O-α-cumyl O-ethyl, O-vinyl and O-isopropenyl peroxycarbonates (percarbonates) have been prepared from the corresponding chloroformates.Their decompositions have been studied in triisopropylbenzene and di-n-butyl phtalate as solvents; in both cases the main process was the heterolysis of the peroxydic bond (Criegee rearrangement) which gave 2-phenoxy propene.Kinetic studies have been performed using Differential Scanning Microcalorimetry; they have shown that the decomposition of O,O-α-cumyl O-ethyl percarbonate is faster in di-butyl phtalate than in triisopropylbenzene and that the rate constants depend on the initial concentrations of the solutions.From both chemical and kinetic data it has been concluded that the studied percarbonates cannot act as free radical initiators even in non polar media.