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Sigma-Aldrich

3,5-Dibenzyloxyacetophenone

98%

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About This Item

Linear Formula:
(C6H5CH2O)2C6H3COCH3
CAS Number:
28924-21-2
Molecular Weight:
332.39
EC Number:
249-315-7
MDL number:
MFCD00004777
UNSPSC Code:
12352100
PubChem Substance ID:
24852887
NACRES:
NA.22

Assay

98%

form

powder

mp

60-62 °C (lit.)

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

Certificates of Analysis (COA)

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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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