M7797
4′-Methoxyflavanone
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About This Item
Empirical Formula (Hill Notation):
C16H14O3
CAS Number:
Molecular Weight:
254.28
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Assay
≥97% (TLC)
SMILES string
COc1ccc(cc1)C2CC(=O)c3ccccc3O2
InChI
1S/C16H14O3/c1-18-12-8-6-11(7-9-12)16-10-14(17)13-4-2-3-5-15(13)19-16/h2-9,16H,10H2,1H3
InChI key
QIUYUYOXCGBABP-UHFFFAOYSA-N
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Steluta Gosav et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 172, 115-125 (2016-04-28)
The aim of this work is to characterize a quite novel 3-dithiocarbamic flavonoid by vibrational spectroscopy in conjunction with Density Functional Theory (DFT) calculations. Quantum mechanics calculations of energies, geometries and vibrational wavenumbers in the ground state were carried out
Jinyan Ye et al.
European journal of pharmacology, 852, 151-158 (2019-02-27)
Inflammation plays an important role in acute lung injury (ALI). Hesperetin (HES), a natural flavanone and an aglycone of hesperidin, has established potent anti-inflammatory activity. The aim of this study was to evaluate the potential protective effect of HES on
Kapil K Patil et al.
International journal of biological macromolecules, 98, 730-738 (2017-02-14)
On the eve of increasing incidence of diabetes mellitus and related complications, the search for novel, safe and alternatives therapeutic approaches are evolving. In the present investigation, a panel of ten dietary flavonoids such as 4'-methoxyflavanone, formononetin, hesperetin, hesperidin, naringenin
Mariana Silva et al.
Journal of chromatography. A, 1490, 166-176 (2017-02-17)
In this paper a chiral stationary phase (CSP) was prepared by the immobilization of a β-CD derivative (3,5-dimethylphenylcarbamoylated β-CD) onto the surface of amino-functionalized spherical ordered mesoporous silica (denoted as SM) via a urea linkage using the Staudinger reaction. The
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