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Merck
CN

798282

Sigma-Aldrich

4,7-二溴-[1,2,5]噻二唑[3,4-c]吡啶

>97%

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关于此项目

经验公式(希尔记法):
C5HBr2N3S
分子量:
294.95
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
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方案

>97%

表单

powder

mp

144-149 °C

SMILES字符串

BrC1=CN=C(Br)C2=NSN=C21

InChI

1S/C5HBr2N3S/c6-2-1-8-5(7)4-3(2)9-11-10-4/h1H

InChI key

LEHZIBSAFRVAJP-UHFFFAOYSA-N

一般描述

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.

应用

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.

象形图

Skull and crossbones

警示用语:

Danger

危险分类

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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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
Solution-processed small-molecule solar cells with 6.7% efficiency
Sun, Yanming; Welch, Gregory C.; Leong, Wei Lin; et al.
Nature Materials, 11(1), 44-48 (2012)

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