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About This Item
Linear Formula:
(C6H5CH2O)2C6H3COCH3
CAS Number:
Molecular Weight:
332.39
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
98%
form
powder
mp
60-62 °C (lit.)
functional group
ketone
phenyl
SMILES string
CC(=O)c1cc(OCc2ccccc2)cc(OCc3ccccc3)c1
InChI
1S/C22H20O3/c1-17(23)20-12-21(24-15-18-8-4-2-5-9-18)14-22(13-20)25-16-19-10-6-3-7-11-19/h2-14H,15-16H2,1H3
InChI key
KOJXGMJOTRYLBD-UHFFFAOYSA-N
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Application
3,5-Dibenzyloxyacetophenone was used in the synthesis of enantiomerically pure B-ring modified analogs of (−)-epicatechin gallate.
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
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James C Anderson et al.
Tetrahedron, 61(32), 7703-7711 (2005-08-08)
Two enantiomerically pure B-ring modified analogues of (-)-epicatechin gallate were synthesised and their modulation of beta-lactam resistance using three strains of methicillin resistant Staphylococcus aureus (BB 568, EMRSA-15 and EMRSA-16) evaluated. Sub-inhibitory concentrations (12.5 and 25 mg/L) of the two
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