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
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
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
Title | Date | PubMed |
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Relaxation processes in an epoxy resin studied by time-resolved optical Kerr effect. | 2002 Jul |
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[Contact allergy to epoxy resins plastics based on materials collected by the Nofer Institute of Occupational Medicine]. | 2003 |
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Enhancing the enantioselectivity of an epoxide hydrolase by directed evolution. | 2004 Jan 22 |
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Infrared optical properties and AFM of spin-cast chitosan films chemically modified with 1,2 Epoxy-3-phenoxy-propane. | 2005 Nov 25 |
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Micellization and drug solubilization in aqueous solutions of a diblock copolymer of ethylene oxide and phenyl glycidyl ether. | 2006 Aug 29 |
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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 |
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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 |
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A novel enantioselective epoxide hydrolase for (R)-phenyl glycidyl ether to generate (R)-3-phenoxy-1,2-propanediol. | 2007 Oct |
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A cold-adapted epoxide hydrolase from a strict marine bacterium, Sphingophyxis alaskensis. | 2008 Aug |
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Screening enantioselective epoxide hydrolase activities from marine microorganisms: detection of activities in Erythrobacter spp. | 2008 Jul-Aug |
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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 |
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Cloning and characterization of an epoxide hydrolase from Novosphingobium aromaticivorans. | 2009 Apr |
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Thermodynamics of surfactants, block copolymers and their mixtures in water: the role of the isothermal calorimetry. | 2009 Jun 29 |
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Chromatographic method for quick estimation of DNA interaction potency of environmental pollutants. | 2009 Oct |
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Biocatalytic resolution of glycidyl phenyl ether using a novel epoxide hydrolase from a marine bacterium, Maritimibacter alkaliphilus KCCM 42376 [corrected]. | 2010 Jun |
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Physical aging of molecular glasses studied by a device allowing for rapid thermal equilibration. | 2010 Nov 7 |
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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
Edited
Sat Dec 16 08:11:37 GMT 2023
by
admin
on
Sat Dec 16 08:11:37 GMT 2023
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Record UNII |
44KJQ1655I
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Record Status |
Validated (UNII)
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Record Version |
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-
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53476
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100000145106
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DTXSID8021145
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122-60-1
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204-557-2
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