assay
98%
mp
55-58 °C (lit.)
functional group
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
InChI key
FYBWRAXKYXTOQC-UHFFFAOYSA-N
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)
"New low band gap compounds comprised of naphthalene diimide and imine units"
Schab-Balcerzak E, et al.
Synthetic Metals, 162(05), 543- 553 (2012)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 576700-1G | 04061826279991 |
| 576700-5G | 04061832628776 |