576700
2,2′-Bithiophen-5-carboxaldehyd
98%
Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise
Alle Fotos(1)
About This Item
Empirische Formel (Hill-System):
C9H6OS2
CAS-Nummer:
Molekulargewicht:
194.27
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
Empfohlene Produkte
![Benzo[b]thiophen-2-Carboxaldehyd 97%](/deepweb/assets/sigmaaldrich/product/structures/321/060/32405a4e-5720-4c6d-91cf-115c747270c4/640/32405a4e-5720-4c6d-91cf-115c747270c4.png)
![Thieno[3,2-b]thiophene-2,5-dicarboxaldehyde 96%](/deepweb/assets/sigmaaldrich/product/structures/137/771/57dfbc98-f02d-4773-bc11-3e8b861ad74b/640/57dfbc98-f02d-4773-bc11-3e8b861ad74b.png)
Assay
98%
mp (Schmelzpunkt)
55-58 °C (lit.)
Funktionelle Gruppe
aldehyde
SMILES String
[H]C(=O)c1ccc(s1)-c2cccs2
InChI
1S/C9H6OS2/c10-6-7-3-4-9(12-7)8-2-1-5-11-8/h1-6H
InChIKey
FYBWRAXKYXTOQC-UHFFFAOYSA-N
Anwendung
2,2′-Bithiophene-5-carboxaldehyde may be used in the synthesis of the following:
- boron dipyrromethene(BODIPY)oligothiophenes via a multi-step reaction process
- (2,2′-bithiophene-5-carbaldehyde)-4-nitrophenylhydrazone(BT-NPH) via reaction with 4-nitrophenylhydrazine
- bithiophene fulleropyrrolidine obtained via refluxing with sarcosine and fullerene
- azomethine phthalic diimides by heating with N,N-bis(4-amino-2,3,5,6-tetramethylphenyl)naphthalene-1,4,5,8-dicarboximide (DANDI)
Lagerklassenschlüssel
13 - Non Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
Eyeshields, Gloves, type N95 (US)
Hier finden Sie alle aktuellen Versionen:
Besitzen Sie dieses Produkt bereits?
In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.
Kunden haben sich ebenfalls angesehen
"New low band gap compounds comprised of naphthalene diimide and imine units"
Schab-Balcerzak E, et al.
Synthetic Metals, 162(05), 543- 553 (2012)
"Enhanced Functionality for Donor?Acceptor Oligothiophenes by means of Inclusion of Bodipy: Synthesis, Electrochemistry, Photophysics, and Model Chemistry"
Collado D, et al.
Chemistry?A European Journal , 17(02), 498-507 (2011)
"Optical nonlinearities and molecular conformations in thiophene-based hydrazone crystals"
Kwon P-O, et al.
The Journal of Physical Chemistry C, 113(34), 15405-15411 (2009)
"The effect of thiophene substituents of fulleropyrrolidine acceptors on the performance of inverted organic solar cells"
Kaunisto.MK, et al.
Synthetic Metals, 195, 193-200 (2014)
Sara S M Fernandes et al.
ACS omega, 3(10), 12893-12904 (2018-11-10)
A series of push-pull heterocyclic N,N-diphenylhydrazones were prepared to study the effect of structural modifications (different π-spacers and electron-withdrawing groups) on the optical (linear and nonlinear) and electronic properties of the molecules. The photovoltaic response of dye-sensitized solar cells assembled
Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..
Setzen Sie sich mit dem technischen Dienst in Verbindung.