Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H10O |
| Molecular Weight | 122.1644 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC=CC(O)=C1C
InChI
InChIKey=QWBBPBRQALCEIZ-UHFFFAOYSA-N
InChI=1S/C8H10O/c1-6-4-3-5-8(9)7(6)2/h3-5,9H,1-2H3
| Molecular Formula | C8H10O |
| Molecular Weight | 122.1644 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| 4-Bromo-methyl-7,8-dimethyl-coumarin. | 2010-11-30 |
|
| Musculoskeletal response to whole-body vibration during fracture healing in intact and ovariectomized rats. | 2010-08 |
|
| Estrogen and raloxifene improve metaphyseal fracture healing in the early phase of osteoporosis. A new fracture-healing model at the tibia in rat. | 2010-02 |
|
| Three dimensional model for N-terminal A domain of DmpR (2-dimethylphenol) protein based on secondary structure prediction and fold recognition. | 2010 |
|
| Solid-phase microextraction Ni-Ti fibers coated with functionalised silica particles immobilized in a sol-gel matrix. | 2009-03-20 |
|
| Determination of gas-phase acidities of dimethylphenols: combined experimental and theoretical study. | 2008-11 |
|
| Disassembly of lignin and chemical recovery in supercritical water and p-cresol mixture. Studies on lignin model compounds. | 2008-04 |
|
| Immunomodulatory effects of mono-, di-, and trimethylphenols in mice. | 2007-03-22 |
|
| Determination of phenolic compounds in wastewater by liquid-phase microextraction coupled with gas chromatography. | 2007-01-27 |
|
| Twisted, Z-shaped perylene bisimide. | 2006-01-25 |
|
| Glucuronidation converts gemfibrozil to a potent, metabolism-dependent inhibitor of CYP2C8: implications for drug-drug interactions. | 2006-01 |
|
| [Degradation of phenols formed during lignin pyrolysis by microfungi of genera Trichoderma and Penicillium]. | 2005-10-26 |
|
| Protein engineering of toluene-o-xylene monooxygenase from Pseudomonas stutzeri OX1 for enhanced chlorinated ethene degradation and o-xylene oxidation. | 2005-09 |
|
| Occupational exposure to aromatic hydrocarbons at a coke plant: Part I. Identification of hydrocarbons in air and their metabolites in urine by a gas chromatography-mass spectrometry method. | 2004-05 |
|
| Synthesis of pyrimidine derivatives possessing an antioxidative property and their inhibitory effects on picryl chloride-induced contact hypersensitivity reaction. | 2003-12 |
|
| Synthesis and SAR studies of potent HIV protease inhibitors containing novel dimethylphenoxyl acetates as P2 ligands. | 2003-11-03 |
|
| Vibrational analysis of substituted phenols: part II. Transferability of valence force constants. | 2002-12 |
|
| Procedure for the quantification of rider peaks. | 2001-09-21 |
|
| Characterization of Rhodococcus opacus R7, a strain able to degrade naphthalene and o-xylene isolated from a polycyclic aromatic hydrocarbon-contaminated soil. | 2001-09 |
|
| Photorelease of HCl from o-methylphenacyl chloride proceeds through the Z-xylylenol. | 2001-08-15 |
|
| Isolation and characterization of a thermotolerant bacterium Ralstonia sp. strain PHS1 that degrades benzene, toluene, ethylbenzene, and o-xylene. | 2001-07 |
|
| Solid-state photochromism and photoreactivity of o- and p-anisaldehydes. Remarkable stabilization of o-xylylenols. | 2001-05-17 |
|
| [Research on a new side-chain liquid crystalline polysiloxane as stationary phase for capillary column gas chromatography]. | 2001-05 |
|
| Determination of Henry's law constants of phenols by pervaporation-flow injection analysis. | 2001-01-01 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:21:39 GMT 2025
by
admin
on
Mon Mar 31 19:21:39 GMT 2025
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| Record UNII |
RLF9YS3586
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| Record Status |
Validated (UNII)
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m11549
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PRIMARY | Merck Index |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (GC)
EP
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