U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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
139594
PubMed

PubMed

TitleDatePubMed
Relaxation processes in an epoxy resin studied by time-resolved optical Kerr effect.
2002 Jul
Improved catalytic performance of Bacillus megaterium epoxide hydrolase in a medium containing Tween-80.
2003 Mar-Apr
Enhancing the enantioselectivity of an epoxide hydrolase by directed evolution.
2004 Jan 22
Chitosan-silica complex membranes from sulfonic acid functionalized silica nanoparticles for pervaporation dehydration of ethanol-water solutions.
2005 Jan-Feb
A novel enantioselective epoxide hydrolase for (R)-phenyl glycidyl ether to generate (R)-3-phenoxy-1,2-propanediol.
2007 Oct
Spectroscopic and quantitative analysis of spiroorthoester synthesis by two-dimensional correlation and multivariate curve resolution methods of NIR data.
2008 Aug
Screening enantioselective epoxide hydrolase activities from marine microorganisms: detection of activities in Erythrobacter spp.
2008 Jul-Aug
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 Nov
Sensitizing capacity and cross-reactivity of phenyl glycidyl ether studied in the guinea-pig maximization test.
2009 Feb
Biocatalytic resolution of glycidyl phenyl ether using a novel epoxide hydrolase from a marine bacterium, Maritimibacter alkaliphilus KCCM 42376 [corrected].
2010 Jun
Physical aging of molecular glasses studied by a device allowing for rapid thermal equilibration.
2010 Nov 7
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 Aug 15
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 Sat Dec 16 08:11:37 GMT 2023
Edited
by admin
on Sat Dec 16 08:11:37 GMT 2023
Record UNII
44KJQ1655I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PHENYL GLYCIDYL ETHER
HSDB  
Systematic 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
AGEFLEX PGE
Brand Name English
(±)-1,2-EPOXY-3-PHENOXYPROPANE
Systematic Name English
Code System Code Type Description
NSC
53476
Created by admin on Sat Dec 16 08:11:37 GMT 2023 , Edited by admin on Sat Dec 16 08:11:37 GMT 2023
PRIMARY
SMS_ID
100000145106
Created by admin on Sat Dec 16 08:11:37 GMT 2023 , Edited by admin on Sat Dec 16 08:11:37 GMT 2023
PRIMARY
EPA CompTox
DTXSID8021145
Created by admin on Sat Dec 16 08:11:37 GMT 2023 , Edited by admin on Sat Dec 16 08:11:37 GMT 2023
PRIMARY
CAS
122-60-1
Created by admin on Sat Dec 16 08:11:37 GMT 2023 , Edited by admin on Sat Dec 16 08:11:37 GMT 2023
PRIMARY
ECHA (EC/EINECS)
204-557-2
Created by admin on Sat Dec 16 08:11:37 GMT 2023 , Edited by admin on Sat Dec 16 08:11:37 GMT 2023
PRIMARY
EVMPD
SUB122936
Created by admin on Sat Dec 16 08:11:37 GMT 2023 , Edited by admin on Sat Dec 16 08:11:37 GMT 2023
PRIMARY
NSC
635
Created by admin on Sat Dec 16 08:11:37 GMT 2023 , Edited by admin on Sat Dec 16 08:11:37 GMT 2023
PRIMARY
FDA UNII
44KJQ1655I
Created by admin on Sat Dec 16 08:11:37 GMT 2023 , Edited by admin on Sat Dec 16 08:11:37 GMT 2023
PRIMARY
HSDB
1821
Created by admin on Sat Dec 16 08:11:37 GMT 2023 , Edited by admin on Sat Dec 16 08:11:37 GMT 2023
PRIMARY
PUBCHEM
31217
Created by admin on Sat Dec 16 08:11:37 GMT 2023 , Edited by admin on Sat Dec 16 08:11:37 GMT 2023
PRIMARY
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966