Compounds > 9,10-bis(phenylethynyl)anthracene
Page last updated: 2024-12-07

9,10-bis(phenylethynyl)anthracene

9,10-bis(phenylethynyl)anthracene, also known as BPEA, is a fluorescent organic molecule with a rigid, planar structure. It has been studied extensively for its potential applications in organic light-emitting diodes (OLEDs), organic solar cells, and as a sensor for various analytes. BPEA exhibits strong fluorescence in the blue region of the visible spectrum, making it a promising candidate for blue-emitting OLEDs. Its synthesis typically involves a Sonogashira coupling reaction between 9,10-dibromoanthracene and phenylacetylene. BPEA is also known for its high thermal stability and good solubility in organic solvents. Researchers are interested in exploring its photophysical properties, investigating its potential for energy transfer, and developing novel materials based on its unique structural features.'
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Cross-References

ID SourceID
PubMed CID82338
CHEBI ID51675
MeSH IDM0541805

Synonyms (36)

Synonym
einecs 233-210-8
9,10-bis(phenylethynyl)anthracene ,
10075-85-1
anthracene, 9,10-bis(2-phenylethynyl)-
CHEBI:51675
bis(phcc)-anthracene
9,10-bis(phenylethynyl)anthracene, 97%
AC-11565
9,10-bis-(phenylethynyl)anthracene
zhbofznnpznwgb-uhfffaoysa-
inchi=1/c30h18/c1-3-11-23(12-4-1)19-21-29-25-15-7-9-17-27(25)30(28-18-10-8-16-26(28)29)22-20-24-13-5-2-6-14-24/h1-18h
P1137
9,10-bis(2-phenylethynyl)anthracene
A800270
AKOS004910146
fc8jdb70dq ,
anthracene, 9,10-bis(phenylethynyl)-
9,10-bis(phenylvinyl)anthracene
unii-fc8jdb70dq
bpea cpd
bpea
FT-0621585
9,10-bis(2-phenylethynyl)anthracene [mi]
DTXSID3064936
SY015099
mfcd00012050
J-650369
W-108941
9,10-bis(phenylethynyl)anthracene #
CS-0010178
Q274980
AS-15612
AMY22869
bpea;9,10-bis(phenylethynyl)anthracene (bpea )
SB66561
9,10-bis-phenylethynyl-anthracene
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
fluorochromeA fluorescent dye used to stain biological specimens.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (3)

ClassDescription
anthracenesCompounds containing an anthracene skeleton.
arylacetyleneAn acetylene with the general formula R(1)-C#C-R(2) where at least one of R(1) or R(2) is an aryl group.
benzenesAny benzenoid aromatic compound consisting of the benzene skeleton and its substituted derivatives.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (9)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (11.11)29.6817
2010's8 (88.89)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 33.64

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index33.64 (24.57)
Research Supply Index2.30 (2.92)
Research Growth Index5.53 (4.65)
Search Engine Demand Index38.01 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (33.64)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other9 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
benzene
[no description available]		2.0810aromatic annulene;
benzenes;
volatile organic compound		carcinogenic agent;
environmental contaminant;
non-polar solvent
indoleacetic acid
indoleacetic acid: RN given refers to unlabeled parent cpd; structure in Merck Index, 9th ed, #4841. auxin : Any of a group of compounds, both naturally occurring and synthetic, that induce cell elongation in plant stems (from Greek alphaupsilonxialphanuomega, "to grow").. indole-3-acetic acid : A monocarboxylic acid that is acetic acid in which one of the methyl hydrogens has been replaced by a 1H-indol-3-yl group.		2.110indole-3-acetic acids;
monocarboxylic acid		auxin;
human metabolite;
mouse metabolite;
plant hormone;
plant metabolite
urea
pseudourea: clinical use; structure. isourea : A carboximidic acid that is the imidic acid tautomer of urea, H2NC(=NH)OH, and its hydrocarbyl derivatives.		2.110isourea;
monocarboxylic acid amide;
one-carbon compound		Daphnia magna metabolite;
Escherichia coli metabolite;
fertilizer;
flour treatment agent;
human metabolite;
mouse metabolite;
Saccharomyces cerevisiae metabolite
erythrosine
Fluoresceins: A family of spiro(isobenzofuran-1(3H),9'-(9H)xanthen)-3-one derivatives. These are used as dyes, as indicators for various metals, and as fluorescent labels in immunoassays.		2.2110
propane
Propane: A three carbon alkane with the formula H3CCH2CH3.		2.110alkane;
gas molecular entity		food propellant
triethylamine
[no description available]		2.110tertiary amine
rhodamine 6g
rhodamine 6G: RN given refers to HCl		2.0510
dithiothreitol
1,4-dimercaptobutane-2,3-diol : A glycol that is butane-2,3-diol in which a hydrogen from each of the methyl groups is replaced by a thiol group.. 1,4-dithiothreitol : The threo-diastereomer of 1,4-dimercaptobutane-2,3-diol.		2.21101,4-dimercaptobutane-2,3-diol;
butanediols;
dithiol;
glycol;
thiol		chelator;
human metabolite;
reducing agent
n,n'-dibutylurea
N,N'-dibutylurea: structure in first source		2.110
firefly luciferin
Firefly Luciferin: A benzothaizole which is oxidized by LUCIFERASES, FIREFLY to cause emission of light (LUMINESCENCE).. Photinus luciferin : A 1,3-thiazolemonocarboxylic acid consisting of 3,5-dihydrothiophene-4-carboxylic acid having a 6-hydroxybenzothiazol-2-yl group at the 2-position.		2.1101,3-thiazolemonocarboxylic acid;
benzothiazoles;
imidothioate		luciferin
bis(2,4,5-trichloro-6-carbopentoxyphenyl)oxalate
[no description available]		2.0710
diacetyldichlorofluorescein
diacetyldichlorofluorescein: stable storage form of dichlorofluorescein		2.2110
fullerene c60
Fullerenes: A polyhedral CARBON structure composed of around 60-80 carbon atoms in pentagon and hexagon configuration. They are named after Buckminster Fuller because of structural resemblance to geodesic domes. Fullerenes can be made in high temperature such as arc discharge in an inert atmosphere.. fullerene : A compound composed solely of an even number of carbon atoms, which form a cage-like fused-ring polycyclic system with twelve five-membered rings and the rest six-membered rings. The term has been broadened to include any closed cage structure consisting entirely of three-coordinate carbon atoms.		2.0610fullerenegeroprotector
bis(2,4,6-trichlorophenyl)oxalate
bis(2,4,6-trichlorophenyl)oxalate: chemiluminescence reagent		2.0610
zinc hematoporphyrin
[no description available]		2.0610
organophosphonates
hydrogenphosphite : A divalent inorganic anion resulting from the removal of a proton from two of the hydroxy groups of phosphorous acid.		2.110divalent inorganic anion;
phosphite ion
oxalates
Oxalates: Derivatives of OXALIC ACID. Included under this heading are a broad variety of acid forms, salts, esters, and amides that are derived from the ethanedioic acid structure.		2.4720
ConditionIndicatedRelationship StrengthStudiesTrials
Infections, Staphylococcal
[description not available]		02.0610
Staphylococcal Infections
Infections with bacteria of the genus STAPHYLOCOCCUS.		02.0610
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