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

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
Structure of 3,5-XYLENOL

SMILES

CC1=CC(O)=CC(C)=C1

InChI

InChIKey=TUAMRELNJMMDMT-UHFFFAOYSA-N
InChI=1S/C8H10O/c1-6-3-7(2)5-8(9)4-6/h3-5,9H,1-2H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Effect of platelet concentration in platelet-rich plasma on peri-implant bone regeneration.
2004 Apr
Asymmetric synthesis of deoxypolypropionate units via stereoselective hydrogenation of optically active cycloheptatriene.
2004 Nov 25
Structural features of phenol derivatives determining potency for activation of chloride currents via alpha(1) homomeric and alpha(1)beta heteromeric glycine receptors.
2005 Aug
Rapid characterization of microbial biodegradation pathways by FT-IR spectroscopy.
2006 Nov
Data processing and classification analysis of proteomic changes: a case study of oil pollution in the mussel, Mytilus edulis.
2006 Sep 13
Study of a monolithic silica capillary column coated with poly(octadecyl methacrylate) for the reversed-phase liquid chromatographic separation of some polar and non-polar compounds.
2007 Dec 14
Behavior of oxidation in the radiochromic gel dosimeter through photoacoustic technique measurements.
2007 May
Characterization of alkylphenol metabolites in fish bile by enzymatic treatment and HPLC-fluorescence analysis.
2008 Apr
Versatile scorpionates and new developments in the denticity changes of NNCp hybrid scorpionate/cyclopentadienyl ligands in Sc and Y compounds: from kappa1-Neta5-Cp to kappa2-NNeta5-Cp.
2008 Jun 2
Lanthanide complexes for magnetic resonance and optical molecular imaging.
2009 Dec
Simple and sensitive determination of 2,4-xylenol in surface water samples from river and sea by gas chromatography-mass spectrometry.
2009 Feb
Iron(III) complexes of tripodal monophenolate ligands as models for non-heme catechol dioxygenase enzymes: correlation of dioxygenase activity with ligand stereoelectronic properties.
2009 Sep 21
Patents
Name Type Language
3,5-XYLENOL
Systematic Name English
XYLENOL, 3,5-
Systematic Name English
3,5-DIMETHYLPHENOL
HSDB  
Systematic Name English
XYLENOL 3,5-DIMETHYLPHENOL [MI]
Common Name English
1-HYDROXY-3,5-DIMETHYLBENZENE
Systematic Name English
3,5-DIMETHYLPHENOL [USP IMPURITY]
Common Name English
NSC-9268
Code English
METACRESOL IMPURITY J [EP IMPURITY]
Common Name English
XYLENOL 3,5-DIMETHYLPHENOL
MI  
Systematic Name English
PHENOL, 3,5-DIMETHYL-
Systematic Name English
1,3,5-XYLENOL
Common Name English
3,5-DIMETHYLPHENOL [HSDB]
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
203-606-5
Created by admin on Fri Dec 15 17:54:16 GMT 2023 , Edited by admin on Fri Dec 15 17:54:16 GMT 2023
PRIMARY
MERCK INDEX
m11549
Created by admin on Fri Dec 15 17:54:16 GMT 2023 , Edited by admin on Fri Dec 15 17:54:16 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID1025148
Created by admin on Fri Dec 15 17:54:16 GMT 2023 , Edited by admin on Fri Dec 15 17:54:16 GMT 2023
PRIMARY
CHEBI
38572
Created by admin on Fri Dec 15 17:54:16 GMT 2023 , Edited by admin on Fri Dec 15 17:54:16 GMT 2023
PRIMARY
HSDB
5385
Created by admin on Fri Dec 15 17:54:16 GMT 2023 , Edited by admin on Fri Dec 15 17:54:16 GMT 2023
PRIMARY
NSC
9268
Created by admin on Fri Dec 15 17:54:16 GMT 2023 , Edited by admin on Fri Dec 15 17:54:16 GMT 2023
PRIMARY
CAS
108-68-9
Created by admin on Fri Dec 15 17:54:16 GMT 2023 , Edited by admin on Fri Dec 15 17:54:16 GMT 2023
PRIMARY
FDA UNII
ONA760G0WA
Created by admin on Fri Dec 15 17:54:16 GMT 2023 , Edited by admin on Fri Dec 15 17:54:16 GMT 2023
PRIMARY
MESH
C016834
Created by admin on Fri Dec 15 17:54:16 GMT 2023 , Edited by admin on Fri Dec 15 17:54:16 GMT 2023
PRIMARY
PUBCHEM
7948
Created by admin on Fri Dec 15 17:54:16 GMT 2023 , Edited by admin on Fri Dec 15 17:54:16 GMT 2023
PRIMARY