215341
3,5-二苄氧基苯乙酮
98%
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线性分子式:
(C6H5CH2O)2C6H3COCH3
化学文摘社编号:
分子量:
332.39
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
249-315-7
MDL number:
Assay:
98%
Form:
powder
InChI key
KOJXGMJOTRYLBD-UHFFFAOYSA-N
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
SMILES string
CC(=O)c1cc(OCc2ccccc2)cc(OCc3ccccc3)c1
assay
98%
form
powder
mp
60-62 °C (lit.)
functional group
ketone, phenyl
Application
3,5-Dibenzyloxyacetophenone was used in the synthesis of enantiomerically pure B-ring modified analogs of (−)-epicatechin gallate.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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