26397-37-5

Basic information

• Product Name: Methoxy, phenyl-
• CAS NO: 26397-37-5
• Molecular Formula: C7H7O
• Molecular Weight: 109.148
• Mol File: 26397-37-5.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Methoxy, phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Methoxy, phenyl-(26397-37-5)
• EPA Substance Registry System: Methoxy, phenyl-(26397-37-5)

Safety Data

• Hazardous Substances Data: 26397-37-5(Hazardous Substances Data)

Upstream product

• 13822-09-8 benzyl peroxide 
• 4399-88-6 Benzylperoxyradikal 
• 2154-56-5 benzyl radical 
• 140-11-4 Benzyl acetate 
• 2143-58-0 methylperoxy radical 

Downstream Products

• 1233319-94-2 BnOP_.(Oi-Pr)3 
• 1233319-90-8 BnOP_.(OMe)3 
• 1233319-92-0 BnOP_.(OEt)3 
• 100-51-6 benzyl alcohol 
• 25087-46-1 methanesulfinyl-methyl 
• 35942-63-3 quinuclidinyl radical 
• 220418-56-4 C₁₀H₂₀N 
• 90265-29-5 tripropylamine 
• 26374-14-1 1-diethylamino-ethyl 
• 2406-15-7 α-hydroxybenzyl radical 
• 4971-41-9 hydroxy-diphenyl-methyl 

Relevant articles and documents

Reactions of the cumyloxyl and benzyloxyl radicals with strong hydrogen bond acceptors. Large enhancements in hydrogen abstraction reactivity determined by substrate/radical hydrogen bonding

A kinetic study on hydrogen abstraction from strong hydrogen bond acceptors such as DMSO, HMPA, and tributylphosphine oxide (TBPO) by the cumyloxyl (CumO?) and benzyloxyl (BnO?) radicals was carried out in acetonitrile. The reactions

Diffusion controlled hydrogen atom abstraction from tertiary amines by the benzyloxyl radical. the importance of C-H/N hydrogen bonding

The rate constants for H-atom abstraction (kH) from 1,4-cyclohexadiene (CHD), triethylamine (TEA), triisobutylamine (TIBA), and DABCO by the cumyloxyl (CumO?) and benzyloxyl (BnO ?) radicals were measured. Comparable ksub

Determination of the Enthalpies of Formation of C6H5CH2O·, p-CH3OC6H4CH2O·, and C6H5CHOH Radicals by Photoionization Mass Spectrometry

The enthalpies of formation (kJ mol-1) of PhCH2O· (125), p-CH3OC6H4CH2O· (-37), and PhCHOH radicals (28) were determined from the energies of appearance of the corresponding fragment ions. The reliability of these data is confirmed by the coincidence of the experimental results with those calculated by the method of isodesmic reactions.