InChI
1S/C9H6OS2/c10-6-7-3-4-9(12-7)8-2-1-5-11-8/h1-6H
SMILES string
[H]C(=O)c1ccc(s1)-c2cccs2
InChI key
FYBWRAXKYXTOQC-UHFFFAOYSA-N
assay
98%
mp
55-58 °C (lit.)
functional group
aldehyde
Application
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)
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
"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)
"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)
"New low band gap compounds comprised of naphthalene diimide and imine units"
Schab-Balcerzak E, et al.
Synthetic Metals, 162(05), 543- 553 (2012)
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
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