69061
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
PubChem Substance ID:
UNSPSC Code:
12352200
Beilstein/REAXYS Number:
1971738
MDL number:
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
assay
≥97.0% (HPLC)
form
powder
mp
49-53 °C
Application
Dihydropinosylvin monomethyl ether may be used in studies of stilbenoid chemistry and function.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2
Storage Class
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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