CHEBI:36007 - trans-stilbene

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name trans-stilbene
ChEBI ID CHEBI:36007
ChEBI ASCII Name trans-stilbene
Definition The trans-isomer of stilbene.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Wikipedia License
Waiting for wikipedia content
Read full article at Wikipedia
Formula C14H12
Net Charge 0
Average Mass 180.24508
Monoisotopic Mass 180.09390
InChI InChI=1S/C14H12/c1-3-7-13(8-4-1)11-12-14-9-5-2-6-10-14/h1-12H/b12-11+
InChIKey PJANXHGTPQOBST-VAWYXSNFSA-N
SMILES c1ccc(cc1)\C=C\c1ccccc1
ChEBI Ontology
Outgoing trans-stilbene (CHEBI:36007) is a stilbene (CHEBI:26775)
Incoming N-(trans-4'-nitro-4-stilbenyl)-N-methyl-5-aminopentanoic acid (CHEBI:46151) has parent hydride trans-stilbene (CHEBI:36007)
trans-pinosylvin (CHEBI:17323) has parent hydride trans-stilbene (CHEBI:36007)
trans-stilben-4-ol (CHEBI:35101) has parent hydride trans-stilbene (CHEBI:36007)
trans-stilbene-4,4'-diol (CHEBI:36012) has parent hydride trans-stilbene (CHEBI:36007)
piceatannol (CHEBI:28814) has parent hydride trans-stilbene (CHEBI:36007)
pterostilbene (CHEBI:8630) has parent hydride trans-stilbene (CHEBI:36007)
IUPAC Name
1,1'-[(1E)-ethene-1,2-diyl]dibenzene
Synonyms Sources
(E)-1,2-diphenylethylene NIST Chemistry WebBook
(E)-stilbene NIST Chemistry WebBook
1,1'-(E)-ethene-1,2-diyldibenzene ChEBI
[(E)-2-phenylethenyl]benzene NIST Chemistry WebBook
trans-1,2-diphenylethylene ChemIDplus
trans-α,β-diphenylethylene NIST Chemistry WebBook
trans-stilbene ChemIDplus
Manual Xrefs Databases
(E)-Stilbene Wikipedia
C00037932 KNApSAcK
View more database links
Registry Numbers Types Sources
103-30-0 CAS Registry Number ChemIDplus
103-30-0 CAS Registry Number NIST Chemistry WebBook
1616740 Beilstein Registry Number ChemIDplus
4381 Gmelin Registry Number Gmelin
Citations Waiting for Citations Types Sources
32201774 PubMed citation Europe PMC
32662469 PubMed citation Europe PMC
33564098 PubMed citation Europe PMC
Last Modified
05 March 2021