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Merck
CN

419753

7-Hydroxyflavanone

98%

Synonym(s):

7-Hydroxy-2-phenylchroman-4-one

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About This Item

Empirical Formula (Hill Notation):
C15H12O3
CAS Number:
6515-36-2
Molecular Weight:
240.25
NACRES:
NA.22
PubChem Substance ID:
24866274
UNSPSC Code:
12352100
MDL number:
MFCD00017487
Assay:
98%
Form:
solid

Key Documents

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functional group

ketone, phenyl

InChI

1S/C15H12O3/c16-11-6-7-12-13(17)9-14(18-15(12)8-11)10-4-2-1-3-5-10/h1-8,14,16H,9H2

SMILES string

Oc1ccc2C(=O)CC(Oc2c1)c3ccccc3

InChI key

SWAJPHCXKPCPQZ-UHFFFAOYSA-N

assay

98%

form

solid

mp

188-190 °C (lit.)

Quality Level

100

Gene Information

mouse ... Maoa(17161)
rat ... Aldh1a2(116676)

Related Categories

Application

7-Hydroxyflavanone has been used for the stereoisomeric separation of flavonoids using polysaccharide-based chiral stationary phases by nano-liquid chromatography (nano-LC).

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKCJ6847
MKBH4022V
MKBF5727V
05902ME
06627MI

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Tomasz Wróblewski et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 215, 81-87 (2019-03-02)
In this work the photophysical properties of 7-hydroxyflavanone in acetonitrile, ethanol and methanol have been studied. The quantum chemical calculations as well as the experimental measurements have been performed. The absorption and emission spectra have been obtained for 7-hydroxyflavanone dissolved
F R Cross
Journal of cell science. Supplement, 12, 117-127 (1989-01-01)
The DAF1-1 mutation reduces cell size and reduces or eliminates G1 phase in Saccharomyces cerevisiae, and results in alpha-factor resistance. DAF1-1 cells transferred into low cycloheximide express an increased G1 phase in their cycle, suggesting that G1 regulation is present
Přemysl Mladěnka et al.
Journal of inorganic biochemistry, 105(5), 693-701 (2011-04-01)
Flavonoids have been demonstrated to possess miscellaneous health benefits which are, at least partly, associated with iron chelation. In this in vitro study, 26 flavonoids from different subclasses were analyzed for their iron chelating activity and stability of the formed
[Microbial kinetics: experiences with Staphylococcus aureus ATCC 25 293 and bacteriostatic drugs].
N B Pappano et al.
Revista latinoamericana de microbiologia, 29(4), 367-372 (1987-10-01)
Edyta Kostrzewa-Susłow et al.
TheScientificWorldJournal, 2012, 254929-254929 (2012-06-02)
Microbial transformations of racemic 7-hydroxyflavanone using strains of genus Aspergillus (A. niger KB, A. niger 13/5, A. ochraceus 456) and the species Penicillium chermesinum 113 were studied. The products of O-methylation, O-methylation along with hydroxylation at C-3' and C-4', reduction
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