stilbene
pair of cis–trans isomers
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stilbene
Summary
stilbene is a group of stereoisomers[1]. stilbene draws 3 Wikipedia views per month (group_of_stereoisomers category, ranking #215 of 1,063).[2]
Key Facts
- stilbene's instance of is recorded as group of stereoisomers[3].
- stilbene's instance of is recorded as group of isomeric entities[4].
- stilbene's CAS Registry Number is recorded as 588-59-0[5].
- stilbene's EC number is recorded as 209-621-3[6].
- stilbene's canonical SMILES is recorded as C1=CC=C(C=C1)C=CC2=CC=CC=C2[7].
- stilbene's InChI is recorded as InChI=1S/C14H12/c1-3-7-13(8-4-1)11-12-14-9-5-2-6-10-14/h1-12H[8].
- stilbene's InChIKey is recorded as PJANXHGTPQOBST-UHFFFAOYSA-N[9].
- stilbene's chemical formula is recorded as C₁₄H₁₂[10].
- stilbene's subclass of is recorded as stilbenoid[11].
- stilbene's part of is recorded as stilbene metabolic process[12].
- stilbene's part of is recorded as stilbene biosynthetic process[13].
- stilbene's part of is recorded as stilbene catabolic process[14].
- stilbene's Commons category is recorded as Stilbene[15].
- stilbene's has part is recorded as 1,1-Diphenylethene[16].
- stilbene's has part is recorded as (E)-stilbene[17].
- stilbene's has part is recorded as (Z)-stilbene[18].
- stilbene's ChemSpider ID is recorded as 11018[19].
- stilbene's PubChem CID is recorded as 11502[20].
- stilbene's ChEBI ID is recorded as 26775[21].
- stilbene's found in taxon is recorded as Alnus sieboldiana[22].
- stilbene's found in taxon is recorded as Petiveria alliacea[23].
- stilbene's found in taxon is recorded as Pinus taeda[24].
- stilbene's found in taxon is recorded as Alnus firma[25].
- stilbene's found in taxon is recorded as Erythrina poeppigiana[26].
- stilbene's Art & Architecture Thesaurus ID is recorded as 300380571[27].
Why It Matters
stilbene draws 3 Wikipedia views per month (group_of_stereoisomers category, ranking #215 of 1,063).[2] stilbene has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[28] stilbene is known by 7 alternative names across languages and contexts.[29]