798282
4,7-Dibromo-[1,2,5]thiadiazolo[3,4-c]pyridine
>97%
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About This Item
Empirical Formula (Hill Notation):
C5HBr2N3S
Molecular Weight:
294.95
UNSPSC Code:
12352103
PubChem Substance ID:
MDL number:
Assay:
>97%
Form:
powder
Product Name
4,7-Dibromo-[1,2,5]thiadiazolo[3,4-c]pyridine, >97%
InChI
1S/C5HBr2N3S/c6-2-1-8-5(7)4-3(2)9-11-10-4/h1H
SMILES string
BrC1=CN=C(Br)C2=NSN=C21
InChI key
LEHZIBSAFRVAJP-UHFFFAOYSA-N
assay
>97%
form
powder
mp
144-149 °C
Application
4,7-Dibromo-[1,2,5]thiadiazolo[3,4-c]pyridine can be used in the synthesis of panchromatic organic for dye sensitized solar cells (DSSCs).
This product is used in the synthesis of photoactive acceptor part in low band gap conjugated polymers and oligomers for high performance OPV devices.
General description
4,7-Dibromo-[1,2,5]thiadiazolo[3,4-c]pyridine is a thiadiazolo[3,4-c]pyridine based material that is used as an electron deficient group for organic electronic applications.
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Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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New simple panchromatic dyes based on thiadiazolo [3, 4-c] pyridine unit for dye-sensitized solar cells
Hua Y, et al.
Dyes and Pigments, 102(48), 196-203 (2014)
Gregory C Welch et al.
Journal of the American Chemical Society, 135(6), 2298-2305 (2013-01-10)
A comparison of two classes of small molecules relevant to the field of organic electronics is carried out at the molecular and supramolecular levels. First, two molecules that differ only in the position of a pyridyl N-atom within an acceptor
Regioregular pyridyl [2, 1, 3] thiadiazole-co-indacenodithiophene conjugated polymers
Wen W, et al.
Chemical Communications (Cambridge, England), 49(65), 7192-7194 (2013)
Nicolas Blouin et al.
Journal of the American Chemical Society, 130(2), 732-742 (2007-12-22)
On the basis of theoretical models and calculations, several alternating polymeric structures have been investigated to develop optimized poly(2,7-carbazole) derivatives for solar cell applications. Selected low band gap alternating copolymers have been obtained via a Suzuki coupling reaction. A good
Chalcogenodiazolo [3, 4-c] pyridine based donor-acceptor-donor polymers for green and near-infrared electrochromics
Ming S, et al.
Polym. Chem., 6(48), 8248-8258 (2015)
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