Skip to Content
MilliporeSigma
All Photos(2)

Key Documents

View All Documentation

215341

Sigma-Aldrich

3,5-Dibenzyloxyacetophenone

98%

Sign Into View Organizational & Contract Pricing
All Photos(2)

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

Looking for similar products? Visit Product Comparison Guide

Application

3,5-Dibenzyloxyacetophenone was used in the synthesis of enantiomerically pure B-ring modified analogs of (−)-epicatechin gallate.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service