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

• 7074-00-2 peroxybenzoic acid phenylisopropyl ester 
• 102653-79-2 3-phenoxy-crotonic acid 
• 80-15-9 Cumene hydroperoxide 
• 74-99-7 prop-1-yne 
• 108-95-2 phenol 
• 57422-37-4 3-phenoxy-crotonic acid ethyl ester 
• 557-93-7 2-bromoprop-1-ene 
• 100-67-4 potassium phenolate 
• 78-75-1 1,2-Dibromopropane 
• 139-02-6 sodium phenoxide 
• 857335-90-1 1-iodo-2-isopropoxybenzene 
• 463-49-0 1,2-propanediene 
• 7732-18-5 water 
• 17333-73-2 phenylium 

Downstream Products

• 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 
• 98995-25-6 (α-chloro-isopropyl)-phenyl ether 
• 10277-93-7 2-isopropenylphenol 
• 144330-59-6 pentacarbonyl{(phenyl)(methyl)(phenyloxy)1,2-diselenolane}tungsten 
• 5026-12-0 2-(2-hydroxyphenyl)-2,4,4-trimethylchroman 
• 88-69-7 2-(1-methylethyl)phenol 
• 100519-82-2 (1,1-dimethyl-butyl)-phenyl ether 
• 81634-59-5 2-methyl-2-phenoxybutane 
• 144866-83-1 (2R,3E)-(-)-1-methylamino-2-(2'-phenoxy-isopropyl)oxypentene 

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.

Organophosphorus Antioxidants. I. Kinetics and Mechanism of the Decomposition of Alkylhydroperoxides by o-Phenylene Phosphites and Phosphates

The reaction mechanism of 2-(2,6-di-tert-butyl-4-methyl-phenoxyl)-1,3,2-benzo-dioxaphosphole (1) with cumyl and t-butyl hydroperoxide has been studied kinetically by means of 31P-n.m.r. spectroscopy and high pressure liquid chromatography. 1 reacts with cumyl hydroperoxide to give the corresponding 2-oxide (2) which with more hydroperoxide and/or water forms the open chained phosphate ester 5.This acidic phosphate decomposes hydroperoxide catalytically.The kinetic parameters of the separate reaction steps are given.The ionic mechanism of hydroperoxide decomposition is accompanied by a homolytic one in a minor proportion.