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Merck
CN

69061

Sigma-Aldrich

Dihydropinosylvin monomethyl ether

≥97.0% (HPLC)

Synonym(s):

3-Hydroxy-5-methoxybibenzyl, 3-Methoxy-5-(2-phenylethyl)phenol

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About This Item

Empirical Formula (Hill Notation):
C15H16O2
CAS Number:
Molecular Weight:
228.29
Beilstein:
1971738
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
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Assay

≥97.0% (HPLC)

form

powder

mp

49-53 °C

SMILES string

COc1cc(O)cc(CCc2ccccc2)c1

InChI

1S/C15H16O2/c1-17-15-10-13(9-14(16)11-15)8-7-12-5-3-2-4-6-12/h2-6,9-11,16H,7-8H2,1H3

InChI key

HPEFWCAKFRCLBD-UHFFFAOYSA-N

Application

Dihydropinosylvin monomethyl ether may be used in studies of stilbenoid chemistry and function.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

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J Fliegmann et al.
Plant molecular biology, 18(3), 489-503 (1992-02-01)
Chalcone synthase (CHS) and stilbene synthase (STS) are closely related polyketide synthases which are key enzymes in the biosynthesis of flavonoids and stilbenes. Scots pine (Pinus sylvestris) is an interesting plant for a direct comparison of the enzymes. It not
L E Lindberg et al.
Journal of industrial microbiology & biotechnology, 31(3), 137-147 (2004-04-28)
Hydrophilic knotwood extracts from 18 wood species were assessed in disc diffusion and liquid culture tests for antibacterial effects against three species of paper mill bacteria. The Pinus sylvestris, P. resinosa, P. contorta, and P. banksiana extracts decreased or inhibited
Michael Adams et al.
Journal of natural products, 68(1), 83-85 (2005-02-01)
Fifteen stilbenoids and two alkaloids from Stemona collinsae, S. tuberosa, and S. peirrei were tested alongside the commercially available stilbenoids resveratrol and pinosylvin for inhibition of leukotriene formation in an ex vivo test system based on activated human neutrophilic granulocytes.

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