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D206008

Sigma-Aldrich

trans,trans-1,4-Diphenyl-1,3-butadien

98%

Synonym(e):

β,β′-Bistyryl, DPB

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About This Item

Lineare Formel:
C6H5CH=CHCH=CHC6H5
CAS-Nummer:
538-81-8
Molekulargewicht:
206.28
Beilstein:
1905939
MDL-Nummer:
MFCD00004791
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24893612
NACRES:
NA.22

Qualitätsniveau

200

Assay

98%

Form

crystals

bp

350 °C (lit.)

mp (Schmelzpunkt)

150-152 °C (lit.)

SMILES String

c1ccc(cc1)\C=C\C=C\c2ccccc2

InChI

1S/C16H14/c1-3-9-15(10-4-1)13-7-8-14-16-11-5-2-6-12-16/h1-14H/b13-7+,14-8+

InChIKey

JFLKFZNIIQFQBS-FNCQTZNRSA-N

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Verwandte Kategorien

Anwendung

trans,trans-1,4-Diphenyl-1,3-butadiene can be used as a reactant to synthesize:
  • 2,5-diphenylthiophene by oxidation reaction with potassium sulfide and DMSO.
  • 2-[(3E)-4-Phenyl-2-(phenylmethyl)-3-buten-1-yl]furan via nickel catalyzed hydrobenzylation reaction with furfural in the presence of N2H4.

It can also be used as a ligand to prepare silver(I) coordination polymers by reacting with silver(I) salts.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
BCCF9112
BCCC7683
BCBZ4681
BCBT9349
BCBQ2593V

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Die Dokumentenbibliothek aufrufen

David P Burgner et al.
PloS one, 10(5), e0125342-e0125342 (2015-05-06)
Pathogen-specific and overall infection burden may contribute to atherosclerosis and cardiovascular disease (CVD), but the effect of infection severity and timing is unknown. We investigated whether childhood infection-related hospitalisation (IRH, a marker of severity) was associated with subsequent adult CVD
Liang Chen et al.
Organic letters, 20(23), 7392-7395 (2018-11-22)
A novel, atom economical, and transition-metal-free strategy for the synthesis of thiophenes from substituted buta-1-enes with potassium sulfide has been presented. The reaction achieves double C-S bond formations via cleavage of multiple C-H bonds and provides an efficient approach to
Mustafa Toprakçí et al.
Bioorganic & medicinal chemistry letters, 15(20), 4438-4446 (2005-09-03)
Monoamine oxidase (EC1.4.3.4; MAO) is a mitochondrial outer membrane flavoenzyme that catalyzes the oxidation of biogenic amines. It has two distinct isozymic forms designated MAO-A and MAO-B, each displaying different substrate and inhibitor specificities. They are the well-known targets for
Vikram Agarwal et al.
eLife, 4 (2015-08-13)
MicroRNA targets are often recognized through pairing between the miRNA seed region and complementary sites within target mRNAs, but not all of these canonical sites are equally effective, and both computational and in vivo UV-crosslinking approaches suggest that many mRNAs
Samim Sardar et al.
Scientific reports, 5, 17313-17313 (2015-11-28)
Energy harvesting from solar light employing nanostructured materials offer an economic way to resolve energy and environmental issues. We have developed an efficient light harvesting heterostructure based on poly(diphenylbutadiyne) (PDPB) nanofibers and ZnO nanoparticles (NPs) via a solution phase synthetic
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Global Trade Item Number

SKUGTIN
D206008-100G
D206008-25G4061833561485
D206008-5G4061833317488

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