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Details Pinosylvin

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Role	Reference Substance
name	Pinosylvin
MPIMP ID	R000332
stereoisomer
isotopomer	ambient
formula	C14H12O2
molecular mass	212.244
monoisotopic mass	212.08373
InChI	InChI=1S/C14H12O2/c15-13-8-12(9-14(16)10-13)7-6-11-4-2-1-3-5-11/h1-10,15-16H/b7-6+
InChIKey	YCVPRTHEGLPYPB-VOTSOKGWSA-N
supplier	Apin
supplier code	17542P
lot	11403
purity
solubility
general	CAS ,sum formula and weight completed with SciFinder
amount	25
amount unit	MG
store temperature 1	4°C
store temperature 2	4°C
store dry	True
store under argon	False
store in dark	False
contributing author	Boelling C, Max Planck Institute of Molecular Plant Physiology, Department of Molecular Plant Physiology (Prof. Willmitzer L), Am Muehlenberg 1, D-14476 Golm, Germany
date of order	2005-02-28
date in	2005-03-30
date out
date expired
box number	159
application/atom+xml	http://gmd.mpimp-golm.mpg.de/REST/gmd.svc/ReferenceSubstance(guid%27d6cad445-d6f3-47ae-b2cf-2499aca4314a%27)

Synonyms of Pinosylvin

property	value
CAS	22139-77-1
ChEBI ID	CHEBI:17323
ChEBI ontology	has parent hydride trans-stilbene
ChEBI ontology	is a pinosylvin
ChemSpider ID	4444110
MetaCyc	CPD-438
synonym	(E)-3,5-stilbenediol
synonym	(E)-5-(2-phenylethenyl)-1,3-benzenediol
synonym	5-[(1E)-2-phenylethenyl]- 1,3-Benzenediol\|trans-3,5-Dihydroxystilbene
synonym	5-[(1E)-2-phenylethenyl]benzene-1,3-diol
15 synonym(s)
Page of 2 Results per page:

Metabolites mapped to Pinosylvin

metabolite	stereoisomer	isotopomer
no hits!

Replica of Pinosylvin

reference substance	supplier	supplier code	lot
No Reference substances found!

compound timestamp information
deposited	at 8/29/2006 by Hummel J., Max Planck Institute of Molecular Plant Physiology, Bioinformatics, Am Muehlenberg 1, D-14476 Golm, Germany
last changed	at 8/7/2013 by Hummel J., Max Planck Institute of Molecular Plant Physiology, Bioinformatics, Am Muehlenberg 1, D-14476 Golm, Germany
modified by users	Strehmel N., Hummel J.

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