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Details

Stereochemistry RACEMIC
Molecular Formula C9H10O2
Molecular Weight 150.1745
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PHENYL GLYCIDYL ETHER

SMILES

C(OC1=CC=CC=C1)C2CO2

InChI

InChIKey=FQYUMYWMJTYZTK-UHFFFAOYSA-N
InChI=1S/C9H10O2/c1-2-4-8(5-3-1)10-6-9-7-11-9/h1-5,9H,6-7H2

HIDE SMILES / InChI
Molecular Formula C9H10O2
Molecular Weight 150.1745
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Unknown
149124
PubMed

PubMed

TitleDatePubMed
Synthesis, biological evaluation and mechanistic studies of totarol amino alcohol derivatives as potential antimalarial agents.
2012-01-15
Structure--activity relationship between the in vivo skin sensitizing potency of analogues of phenyl glycidyl ether and the induction of Nrf2-dependent luciferase activity in the KeratinoSens in vitro assay.
2011-08-15
Physical aging of molecular glasses studied by a device allowing for rapid thermal equilibration.
2010-11-07
Biocatalytic resolution of glycidyl phenyl ether using a novel epoxide hydrolase from a marine bacterium, Maritimibacter alkaliphilus KCCM 42376 [corrected].
2010-06
Synthesis of silver nanoparticles coated with OH-functionalized organic groups: dispersion and covalent bonding in epoxy networks.
2010-02-02
Reduced sensitizing capacity of epoxy resin systems: a structure-activity relationship study.
2009-11
Chromatographic method for quick estimation of DNA interaction potency of environmental pollutants.
2009-10
Thermodynamics of surfactants, block copolymers and their mixtures in water: the role of the isothermal calorimetry.
2009-06-29
Directed evolution of an enantioselective epoxide hydrolase: uncovering the source of enantioselectivity at each evolutionary stage.
2009-06-03
Cloning and characterization of an epoxide hydrolase from Novosphingobium aromaticivorans.
2009-04
Sensitizing capacity and cross-reactivity of phenyl glycidyl ether studied in the guinea-pig maximization test.
2009-02
Can simultaneous contact allergies to phenyl glycidyl ether and epoxy resins of the bisphenol A/F-types be explained by contamination of the epoxy resins?
2008-11
A cold-adapted epoxide hydrolase from a strict marine bacterium, Sphingophyxis alaskensis.
2008-08
Spectroscopic and quantitative analysis of spiroorthoester synthesis by two-dimensional correlation and multivariate curve resolution methods of NIR data.
2008-08
A novel enantioselective epoxide hydrolase for (R)-phenyl glycidyl ether to generate (R)-3-phenoxy-1,2-propanediol.
2007-10
Screening enantioselective epoxide hydrolase activities from marine microorganisms: detection of activities in Erythrobacter spp.
2007-08-21
Validation of the concentration profiles obtained from the near infrared/multivariate curve resolution monitoring of reactions of epoxy resins using high performance liquid chromatography as a reference method.
2007-03-07
Micellization and drug solubilization in aqueous solutions of a diblock copolymer of ethylene oxide and phenyl glycidyl ether.
2006-08-29
Influence of SDS and two anionic hydrotropes on the micellized state of the triblock copolymer E71G7E71.
2006-04-15
Multivariate curve resolution-alternating least squares and kinetic modeling applied to near-infrared data from curing reactions of epoxy resins: mechanistic approach and estimation of kinetic rate constants.
2006-02
Infrared optical properties and AFM of spin-cast chitosan films chemically modified with 1,2 Epoxy-3-phenoxy-propane.
2005-11-25
Block copolymers of ethylene oxide and phenyl glycidyl ether: micellization, gelation, and drug solubilization.
2005-06-07
Chitosan-silica complex membranes from sulfonic acid functionalized silica nanoparticles for pervaporation dehydration of ethanol-water solutions.
2005-01-11
An attempt to improve diagnostics of contact allergy due to epoxy resin systems. First results of the multicentre study EPOX 2002.
2004-12-21
Enhancing the enantioselectivity of an epoxide hydrolase by directed evolution.
2004-01-22
Improved catalytic performance of Bacillus megaterium epoxide hydrolase in a medium containing Tween-80.
2003-04-05
Two cases of occupational allergic contact dermatitis from a cycloaliphatic epoxy resin in a neat oil: case report.
2003-03-26
[Contact allergy to epoxy resins plastics based on materials collected by the Nofer Institute of Occupational Medicine].
2003
Relaxation processes in an epoxy resin studied by time-resolved optical Kerr effect.
2002-07
Patents

Patents

04582833
1
05064863
3
05110820
1
05496589
2
05707690
1
06432656
4
08039503
5
08765728
1
JP2005514484A
3
JPH02219816A
2
JPH03115331A
1
JPH04145186A
1
JPH0491157A
1
JPH055006A
1
JPH06145298A
2
JPH0649133A
1
JPH07304897A
1
JPH08277385A
1
JPH10218854A
1
JPH10306234A
1
JPH11228659A
1
JPH1160686A
1
JPH1160818A
1
JPS05852344A
1
JPS5557578A
1
JPS56106973A
1
JPS58164607A
1
JPS59117590A
2
JPS59122539A
1
JPS59189178A
1
JPS60115617A
2
JPS6163664A
1
JPS62184009A
1
JPS63295676A
1
JPS6386714A
1
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:55:51 GMT 2025
Edited
by admin
on Mon Mar 31 21:55:51 GMT 2025
Record UNII
44KJQ1655I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PHENYL GLYCIDYL ETHER
HSDB  
Systematic Name English
AGEFLEX PGE
Preferred Name English
NSC-635
Code English
PHENYL GLYCIDYL ETHER [IARC]
Common Name English
.GAMMA.-PHENOXYPROPYLENE OXIDE
Common Name English
PHENYL GLYCIDYL ETHER [HSDB]
Common Name English
NSC-53476
Code English
GLYCIDYL PHENYL ETHER
Systematic Name English
OXIRANE, 2-(PHENOXYMETHYL)-
Systematic Name English
3-PHENOXY-1,2-PROPYLENE OXIDE
Systematic Name English
PHENOL GLYCIDYL ETHER
Systematic Name English
2,3-EPOXYPROPYL PHENYL ETHER
Systematic Name English
BENZENE, (2,3-EPOXYPROPOXY)-
Systematic Name English
PROPANE, 1,2-EPOXY-3-PHENOXY-
Systematic Name English
(±)-1,2-EPOXY-3-PHENOXYPROPANE
Systematic Name English
Code System Code Type Description
NSC
53476
Created by admin on Mon Mar 31 21:55:51 GMT 2025 , Edited by admin on Mon Mar 31 21:55:51 GMT 2025
PRIMARY
SMS_ID
100000145106
Created by admin on Mon Mar 31 21:55:51 GMT 2025 , Edited by admin on Mon Mar 31 21:55:51 GMT 2025
PRIMARY
EPA CompTox
DTXSID8021145
Created by admin on Mon Mar 31 21:55:51 GMT 2025 , Edited by admin on Mon Mar 31 21:55:51 GMT 2025
PRIMARY
CAS
122-60-1
Created by admin on Mon Mar 31 21:55:51 GMT 2025 , Edited by admin on Mon Mar 31 21:55:51 GMT 2025
PRIMARY
ECHA (EC/EINECS)
204-557-2
Created by admin on Mon Mar 31 21:55:51 GMT 2025 , Edited by admin on Mon Mar 31 21:55:51 GMT 2025
PRIMARY
EVMPD
SUB122936
Created by admin on Mon Mar 31 21:55:51 GMT 2025 , Edited by admin on Mon Mar 31 21:55:51 GMT 2025
PRIMARY
NSC
635
Created by admin on Mon Mar 31 21:55:51 GMT 2025 , Edited by admin on Mon Mar 31 21:55:51 GMT 2025
PRIMARY
FDA UNII
44KJQ1655I
Created by admin on Mon Mar 31 21:55:51 GMT 2025 , Edited by admin on Mon Mar 31 21:55:51 GMT 2025
PRIMARY
HSDB
1821
Created by admin on Mon Mar 31 21:55:51 GMT 2025 , Edited by admin on Mon Mar 31 21:55:51 GMT 2025
PRIMARY
PUBCHEM
31217
Created by admin on Mon Mar 31 21:55:51 GMT 2025 , Edited by admin on Mon Mar 31 21:55:51 GMT 2025
PRIMARY
NIH
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