Catalogue Number
BF-P4006
Analysis Method
HPLC,NMR,MS
Specification
98%(HPLC)
Storage
2-8°C
Molecular Weight
242.274
Appearance
Powder
Botanical Source
Dracaena cochinchinensis
Structure Type
Stilbenes
Category
Standards;Natural Pytochemical;API
SMILES
COC1=CC(=CC(=C1)O)C=CC2=CC=C(C=C2)O
Synonyms
mono-methylated resveratrol /3,4'-Dihydroxy-5-methoxy-trans-stilbene /3-[(E)-2-(4-Hydroxyphenyl)vinyl]-5-methoxyphenol /Pinostilbene /Pinostilbene hydrate /3-methoxyresveratrol /trans-3,4'-dihydroxy-5-methoxystilbene /phenol (3-[(E)-2-(4-hydroxyphenyl)ethenyl]-5-methoxy /5,4'-dihydroxy-3-methoxystilbene /trans-Pinostilbene /3-methoxy-4',5-dihydroxy-trans-stilbene /4,3'-dihydroxy-5'-methoxystilbene /Phenol, 3-[(E)-2-(4-hydroxyphenyl)ethenyl]-5-methoxy-
IUPAC Name
3-[(E)-2-(4-hydroxyphenyl)ethenyl]-5-methoxyphenol
Density
1.3±0.1 g/cm3
Solubility
Methanol
Flash Point
228.5±25.4 °C
Boiling Point
454.3±33.0 °C at 760 mmHg
Melting Point
117-118℃
InChl
InChl Key
WGK Germany
RID/ADR
HS Code Reference
2909500000
Personal Projective Equipment
Correct Usage
For Reference Standard and R&D, Not for Human Use Directly.
Meta Tag
provides coniferyl ferulate(CAS#:42438-89-1) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate
10553400
OBJECTIVES: The effect of a community-based physical activity program in Pawtucket, RI, was evaluated relative to one in a comparison community. METHODS: Cross-sectional surveys of 7529 residents of Pawtucket, RI, and 7732 residents of the comparison city were conducted at 2-year intervals during 7 years of intervention. RESULTS: There were no differences in self-reported knowledge of the benefits of physical activity, attempts to increase exercise, or prevalence of physical inactivity between Pawtucket and the comparison community. CONCLUSIONS: Future community-based physical activity interventions should attempt to involve a wider range of individuals.
Effects of a community-based intervention on physical activity: the Pawtucket Heart Health Program.
C B Eaton, K L Lapane, C E Garber, K M Gans, T M Lasater, and R A Carleton
1999 November;
21581440
In the title molecule, C13H13ClN2O2, the heterocyclic ring adopts a flattened boat conformation with the plane through the four coplanar atoms making a dihedral angle of 89.16 (5)° with the benzene ring, which adopts an axial orientation. The carbonyl, acetyl and methyl groups each have an equatorial orientation. In the crystal structure, intermolecular N—H⋯O hydrogen bonds lead to a tape motif. The H atoms of the methyl group at position 6 are disordered over two positions of opposite orientation.
5-Acetyl-4-(2-chlorophenyl)-6-methyl-3,4-dihydropyrimidin-2(1H)-one
N. Anuradha,a A. Thiruvalluvar,a,* K. Pandiarajan,b S. Chitra,b and R. J. Butcherc
2008 Dec 1;
28947840
Diaporthales is an important ascomycetous order comprising phytopathogenic, saprobic, and endophytic fungi, but interfamilial taxonomic relationships are still ambiguous. Despite its cosmopolitan distribution and high diversity with distinctive morphologies, this order has received relativelyiaceae, Macrohilaceae, Melanconidaceae, Pseudoplagiostomaceae, Schizoparmaceae, Stilbosporaceae and Sydowiellaceae. Taxonomic uncertainties among genera are also clarified and recurrent discrepancies in the taxonomic position of families within the Diaporthales are discussed. An updated outline and key to families and genera of the order is presented.
Key words: Multi-gene DNA phylogeny, New taxonomic arrangement, Phytopathogenic fungi, Sordariomycetes, Systematics
Taxonomic novelties: New families: Apiosporopsidaceae Senan. Maharachch. & K.D. Hyde, Apoharknessiaceae Senan. Maharachch. & K.D. Hyde, Asterosporiaceae Senan. Maharachch. & K.D. Hyde, Auratiopycnidiellaceae Senan. Maharachch. & K.D. Hyde, Erythrogloeaceae Senan. Maharachch. & K.D. Hyde, Melanconiellaceae Senan. Maharachch. & K.D. Hyde, Prosopidicolaceae Senan. & K.D. Hyde
New genera: Marsupiomyces Senan. & K.D. Hyde, Microascospora Senan., Camporesi & K.D. Hyde, Phaeoappendicospora Senan., Q.R. Li & K.D. Hyde, Paradiaporthe Senan., Camporesi, & K.D. Hyde, Hyaliappendispora Senan., Camporesi & K.D. Hyde, Chiangraiomyces Senan. & K.D. Hyde
New species: Chiangraiomyces bauhiniae Senan. & K.D. Hyde, Coniella pseudokoreana Senan., Tangthir. & K.D. Hyde, Cytospora centrivillosa Senan., Camporesi & K.D. Hyde, Cytospora junipericola Senan., Camporesi & K.D. Hyde, Cytospora quercicola Senan., Camporesi & K.D. Hyde, Cytospora rosae Senan., Camporesi & K.D. Hyde, Cytospora fraxinigena Senan., Camporesi & K.D. Hyde, Diaporthe litoricola Senan., E.B.G. Jones & K.D. Hyde, Ditopella biseptata R.H. Perera, Senan., Camporesi & K.D. Hyde, Gnomoniopsis agrimoniae Senan., Camporesi & K.D. Hyde, Hyaliappendispora galii Senan., Camporesi & K.D. Hyde, Marsupiomyces epidermoidea R.H. Perera, Senan., Bulgakov & K.D. Hyde, Marsupiomyces quercina Senan., Camporesi & K.D. Hyde, Melanconis italica Senan., Camporesi & K.D. Hyde, Microascospora rubi Senan., Camporesi & K.D. Hyde, Paradiaporthe artemisiae Senan., Camporesi & K.D. Hyde, Phaeoappendicospora thailandensis Senan., Q.R. Li & K.D. Hyde, Plagiostoma jonesii Senan., & K.D. Hyde, Plagiostoma salicicola Senan., Camporesi & K.D. Hyde, Sydowiella urticicola Senan., Camporesi & K.D. Hyde, Tubakia thailandensis Senan., Tangthir., K.D. Hyde
New combinations: Coryneum arausiaca (Fabre) Senan., Maharachch. & K.D. Hyde, Microascospora fragariae (F. Stevens & Peterson) Senan., Maharachch. & K.D. Hyde
Multi-gene DNA phylogeny, New taxonomic arrangement, Phytopathogenic fungi, Sordariomycetes, Systematics
Families of Diaporthales based on morphological and phylogenetic evidence
I.C. Senanayake,1,2,3 P.W. Crous,4 J.Z. Groenewald,4 S.S.N. Maharachchikumbura,5 R. Jeewon,6 A.J.L. Phillips,7 J.D. Bhat,8,9 R.H. Perera,3 Q.R. Li,10 W.J. Li,1,2,3 N. Tangthirasunun,11,12 C. Norphanphoun,3 S.C. Karunarathna,1,2,∗ E. Camporesi,13,14,15 I.S. Manawasighe,16 A.M. Al-Sadi,5 and K.D. Hyde1,2,3
2017 Mar;