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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

PubMed

PubMed

TitleDatePubMed
Relaxation processes in an epoxy resin studied by time-resolved optical Kerr effect.
2002 Jul
[Contact allergy to epoxy resins plastics based on materials collected by the Nofer Institute of Occupational Medicine].
2003
Enhancing the enantioselectivity of an epoxide hydrolase by directed evolution.
2004 Jan 22
Infrared optical properties and AFM of spin-cast chitosan films chemically modified with 1,2 Epoxy-3-phenoxy-propane.
2005 Nov 25
Micellization and drug solubilization in aqueous solutions of a diblock copolymer of ethylene oxide and phenyl glycidyl ether.
2006 Aug 29
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 Feb
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 Mar 7
A novel enantioselective epoxide hydrolase for (R)-phenyl glycidyl ether to generate (R)-3-phenoxy-1,2-propanediol.
2007 Oct
A cold-adapted epoxide hydrolase from a strict marine bacterium, Sphingophyxis alaskensis.
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
Cloning and characterization of an epoxide hydrolase from Novosphingobium aromaticivorans.
2009 Apr
Thermodynamics of surfactants, block copolymers and their mixtures in water: the role of the isothermal calorimetry.
2009 Jun 29
Chromatographic method for quick estimation of DNA interaction potency of environmental pollutants.
2009 Oct
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
Synthesis, biological evaluation and mechanistic studies of totarol amino alcohol derivatives as potential antimalarial agents.
2012 Jan 15
Patents
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
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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