Details
Stereochemistry | ACHIRAL |
Molecular Formula | C9H12O |
Molecular Weight | 136.191 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC(C)=C(O)C(C)=C1
InChI
InChIKey=BPRYUXCVCCNUFE-UHFFFAOYSA-N
InChI=1S/C9H12O/c1-6-4-7(2)9(10)8(3)5-6/h4-5,10H,1-3H3
Molecular Formula | C9H12O |
Molecular Weight | 136.191 |
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 |
---|---|---|
Thermochemical and kinetic studies of a bisphenol antioxidant. | 2001 Aug 10 |
|
Electron-rich phenols for probing the photochemical reactivity of freshwaters. | 2001 Feb 15 |
|
Methylphenols removal from water by low-cost adsorbents. | 2002 Jul 1 |
|
4,6,8,10,16-penta- and 4,6,8,10,16,18-hexamethyldocosanes from the cane beetle antitrogusparvulus--cuticular hydrocarbons with unprecedented structure and stereochemistry. | 2003 Dec 25 |
|
The effect of ring nitrogen atoms on the homolytic reactivity of phenolic compounds: understanding the radical-scavenging ability of 5-pyrimidinols. | 2003 Oct 17 |
|
Key role of the low molecular size fraction of soil humic acids for fluorescence and photoinductive activity. | 2004 Apr 1 |
|
Photosensitized degradation of bisphenol A by dissolved organic matter. | 2004 Nov 15 |
|
Humic substances mediated phototransformation of 2,4,6-trimethylphenol: a catalytic reaction. | 2005 Jun |
|
Novel cuticular hydrocarbons from the cane beetle Antitrogus parvulus--4,6,8,10,16-penta- and 4,6,8,10,16,18-hexamethyldocosanes-unprecedented anti-anti-anti-stereochemistry in the 4,6,8,10-methyltetrad. | 2005 Mar 4 |
|
Selective copper(II)-mediated oxidative coupling of a nucleophilic reagent to the para-methyl group of 2,4,6-trimethylphenol. | 2005 Nov 7 |
|
Synthetic and reaction chemistry of heteroatom stabilized boryl and cationic borylene complexes. | 2006 Jan 14 |
|
Effect of three different cultivars of Lepidium meyenii (Maca) on learning and depression in ovariectomized mice. | 2006 Jun 23 |
|
Data processing and classification analysis of proteomic changes: a case study of oil pollution in the mussel, Mytilus edulis. | 2006 Sep 13 |
|
Gas-phase acidities and O-H bond dissociation enthalpies of phenol, 3-methylphenol, 2,4,6-trimethylphenol, and ethanoic acid. | 2006 Sep 7 |
|
Transformation of polycyclic aromatic hydrocarbons by laccase is strongly enhanced by phenolic compounds present in soil. | 2007 Apr 15 |
|
Column temperature as an active variable in the isocratic, normal-phase high-performance liquid chromatography separation of lipophilic metabolites of nonylphenol ethoxylates. | 2007 Jul 20 |
|
Inhibition of humic substances mediated photooxygenation of furfuryl alcohol by 2,4,6-trimethylphenol. Evidence for reactivity of the phenol with humic triplet excited states. | 2007 Sep 1 |
|
Chemical composition and biological activity of a new type of Brazilian propolis: red propolis. | 2007 Sep 5 |
|
Characterization of alkylphenol metabolites in fish bile by enzymatic treatment and HPLC-fluorescence analysis. | 2008 Apr |
|
Evaluation of photochemical properties of compost humic-like materials. | 2008 Jul |
|
Mono-, di-, tri- and tetranuclear rare earth complexes obtained using a moderately bulky aryloxide ligand. | 2009 Nov 2 |
|
Reactive photoinduced species in estuarine waters. Characterization of hydroxyl radical, singlet oxygen and dissolved organic matter triplet state in natural oxidation processes. | 2010 Jan |
|
Synthesis of fluoro(aryloxo)alkaline earth metal cages by C-F bond activation. | 2010 Jun 28 |
|
Structural diversity in polyamine Lewis base stabilised lithium aryloxides. | 2010 Sep 21 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:34:18 GMT 2023
by
admin
on
Fri Dec 15 19:34:18 GMT 2023
|
Record UNII |
FPZ32614N6
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
JECFA EVALUATION |
2,4,6-TRIMETHYLPHENOL
Created by
admin on Fri Dec 15 19:34:18 GMT 2023 , Edited by admin on Fri Dec 15 19:34:18 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
5353
Created by
admin on Fri Dec 15 19:34:18 GMT 2023 , Edited by admin on Fri Dec 15 19:34:18 GMT 2023
|
PRIMARY | |||
|
1991
Created by
admin on Fri Dec 15 19:34:18 GMT 2023 , Edited by admin on Fri Dec 15 19:34:18 GMT 2023
|
PRIMARY | |||
|
Mesitol
Created by
admin on Fri Dec 15 19:34:18 GMT 2023 , Edited by admin on Fri Dec 15 19:34:18 GMT 2023
|
PRIMARY | |||
|
FPZ32614N6
Created by
admin on Fri Dec 15 19:34:18 GMT 2023 , Edited by admin on Fri Dec 15 19:34:18 GMT 2023
|
PRIMARY | |||
|
DTXSID7022049
Created by
admin on Fri Dec 15 19:34:18 GMT 2023 , Edited by admin on Fri Dec 15 19:34:18 GMT 2023
|
PRIMARY | |||
|
C505148
Created by
admin on Fri Dec 15 19:34:18 GMT 2023 , Edited by admin on Fri Dec 15 19:34:18 GMT 2023
|
PRIMARY | |||
|
10698
Created by
admin on Fri Dec 15 19:34:18 GMT 2023 , Edited by admin on Fri Dec 15 19:34:18 GMT 2023
|
PRIMARY | |||
|
208-419-2
Created by
admin on Fri Dec 15 19:34:18 GMT 2023 , Edited by admin on Fri Dec 15 19:34:18 GMT 2023
|
PRIMARY | |||
|
5677
Created by
admin on Fri Dec 15 19:34:18 GMT 2023 , Edited by admin on Fri Dec 15 19:34:18 GMT 2023
|
PRIMARY | |||
|
527-60-6
Created by
admin on Fri Dec 15 19:34:18 GMT 2023 , Edited by admin on Fri Dec 15 19:34:18 GMT 2023
|
PRIMARY |