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Details

Stereochemistry ACHIRAL
Molecular Formula C8H8O4
Molecular Weight 168.1467
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PHLOROACETOPHENONE

SMILES

CC(=O)C1=C(O)C=C(O)C=C1O

InChI

InChIKey=XLEYFDVVXLMULC-UHFFFAOYSA-N
InChI=1S/C8H8O4/c1-4(9)8-6(11)2-5(10)3-7(8)12/h2-3,10-12H,1H3

HIDE SMILES / InChI

Molecular Formula C8H8O4
Molecular Weight 168.1467
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis of kaempferol 3-O-(3'',6''-di-O-E-p-coumaroyl)-β-D-glucopyranoside, efficient glycosylation of flavonol 3-OH with glycosyl o-alkynylbenzoates as donors.
2010-10-15
Crystal structure and computational analyses provide insights into the catalytic mechanism of 2,4-diacetylphloroglucinol hydrolase PhlG from Pseudomonas fluorescens.
2010-02-12
Simultaneous analysis of vitamins and caffeine in energy drinks by surfactant-mediated matrix-assisted laser desorption/ionization.
2008-08
Rapid screening of anthocyanins in berry samples by surfactant-mediated matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.
2008
Matrix-assisted laser desorption/ionization mass spectrometry of polysaccharides with 2',4',6'-trihydroxyacetophenone as matrix.
2007
Determining enediol compounds in tea using surface-assisted laser desorption/ionization mass spectrometry with titanium dioxide nanoparticle matrices.
2007
Detection of phosphopeptides using Fe(III)-nitrilotriacetate complexes immobilized on a MALDI plate.
2006-03-01
Complete MALDI-ToF MS analysis of cross-linked peptide-RNA oligonucleotides derived from nonlabeled UV-irradiated ribonucleoprotein particles.
2005-12
Rapid separation of antimicrobial metabolites by microchip electrophoresis with UV linear imaging detection.
2005-04-15
Defense responses of Fusarium oxysporum to 2,4-diacetylphloroglucinol, a broad-spectrum antibiotic produced by Pseudomonas fluorescens.
2004-11
Rapid analysis of antimicrobial metabolites monoacetylphloroglucinol and 2,4-diacetylphloroglucinol using capillary zone electrophoresis.
2004-06
Enhanced ionization of phosphorylated peptides during MALDI TOF mass spectrometry.
2004-03-01
Chromone studies. Part 13. Synthesis and electron-impact mass spectrometric studies of 5-hydroxy-2-isopropyl-7-methoxychromone, a constituent of the medicinal plant Baeckea frutescens, and side-chain analogues.
2003-08
Evaluation of the acute and subacute toxicity of a choleretic phloracetophenone in experimental animals.
2002-03-24
Sodium-tolerant matrix for matrix-assisted laser desorption/ionization mass spectrometry and post-source decay of oligonucleotides.
2002
Involvement of gacS and rpoS in enhancement of the plant growth-promoting capabilities of Enterobacter cloacae CAL2 and UW4.
2001-08
Investigating the molecular heterogeneity of polysorbate emulsifiers by MALDI-TOF MS.
2001-07
A rapid polymerase chain reaction-based assay characterizing rhizosphere populations of 2,4-diacetylphloroglucinol-producing bacteria.
2001-01
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:38:59 GMT 2025
Edited
by admin
on Mon Mar 31 19:38:59 GMT 2025
Record UNII
8L7XD8830T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-54927
Preferred Name English
PHLOROACETOPHENONE
Common Name English
2,4,6-TRIHYDROXYACETOPHENONE
Common Name English
ACETOPHLOROGLUCINE
Common Name English
Code System Code Type Description
CAS
480-66-0
Created by admin on Mon Mar 31 19:38:59 GMT 2025 , Edited by admin on Mon Mar 31 19:38:59 GMT 2025
PRIMARY
CHEBI
64344
Created by admin on Mon Mar 31 19:38:59 GMT 2025 , Edited by admin on Mon Mar 31 19:38:59 GMT 2025
PRIMARY
PUBCHEM
68073
Created by admin on Mon Mar 31 19:38:59 GMT 2025 , Edited by admin on Mon Mar 31 19:38:59 GMT 2025
PRIMARY
ECHA (EC/EINECS)
207-556-5
Created by admin on Mon Mar 31 19:38:59 GMT 2025 , Edited by admin on Mon Mar 31 19:38:59 GMT 2025
PRIMARY
MESH
C107067
Created by admin on Mon Mar 31 19:38:59 GMT 2025 , Edited by admin on Mon Mar 31 19:38:59 GMT 2025
PRIMARY
EPA CompTox
DTXSID5060061
Created by admin on Mon Mar 31 19:38:59 GMT 2025 , Edited by admin on Mon Mar 31 19:38:59 GMT 2025
PRIMARY
NSC
54927
Created by admin on Mon Mar 31 19:38:59 GMT 2025 , Edited by admin on Mon Mar 31 19:38:59 GMT 2025
PRIMARY
FDA UNII
8L7XD8830T
Created by admin on Mon Mar 31 19:38:59 GMT 2025 , Edited by admin on Mon Mar 31 19:38:59 GMT 2025
PRIMARY
WIKIPEDIA
2,4,6-TRIHYDROXYACETOPHENONE
Created by admin on Mon Mar 31 19:38:59 GMT 2025 , Edited by admin on Mon Mar 31 19:38:59 GMT 2025
PRIMARY