1239277-96-3

Basic information

• Product Name: 4-BroMo-7-(dibroMoMethyl)benzo[c][1,2,5]thiadiazole
• Synonyms: 4-BroMo-7-(dibroMoMethyl)benzo[c][1,2,5]thiadiazole
• CAS NO: 1239277-96-3
• Molecular Formula: C₇H₃Br₃N₂S
• Molecular Weight: 386.88912
• Mol File: 1239277-96-3.mol
• Article Data: 5

Chemical Properties

• Melting Point: 119-120 °C
• Boiling Point: 400.5±40.0 °C(Predicted)
• Appearance: /
• Density: 2.431±0.06 g/cm3(Predicted)
• PKA: -2.70±0.50(Predicted)
• CAS DataBase Reference: 4-BroMo-7-(dibroMoMethyl)benzo[c][1,2,5]thiadiazole(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BroMo-7-(dibroMoMethyl)benzo[c][1,2,5]thiadiazole(1239277-96-3)
• EPA Substance Registry System: 4-BroMo-7-(dibroMoMethyl)benzo[c][1,2,5]thiadiazole(1239277-96-3)

Safety Data

• Hazardous Substances Data: 1239277-96-3(Hazardous Substances Data)

Usage

General Description

4-Bromo-7-(dibromomethyl)benzo[c][1,2,5]thiadiazole is a chemical compound with the molecular formula C8H3Br3N2S. It is a benzothiadiazole derivative with two bromine atoms and a dibromomethyl group attached to the benzene ring. 4-BroMo-7-(dibroMoMethyl)benzo[c][1,2,5]thiadiazole is commonly used in the field of organic chemistry for its potential applications in materials science, particularly in the development of organic semiconductors and electronic devices. Its unique structure and properties make it a valuable building block for the synthesis of advanced materials with electronic and optoelectronic properties. Overall, 4-Bromo-7-(dibromomethyl)benzo[c][1,2,5]thiadiazole has the potential to contribute to the advancement of technology and scientific research in various fields.

Upstream product

• 2255-80-3 4-bromo-7-methylbenzo[c][1,2,5]thiadiazole 
• 2687-25-4 3-methyl-1,2-benzenediamine 
• 1457-92-7 4-Methyl-2,1,3-benzothiadiazol 

Downstream Products

• 1071224-34-4 7-bromobenzo[c][1,2,5]thiadiazole-4-carboxaldehyde 
• 1335150-10-1 2-((7-bromobenzo[c][1,2,5]thiadiazol-4-yl)methylene)malononitrile 
• 1335150-09-8 2-{[7-(5-(N,N-di-p-tolyl)aminothiophen-2-yl)-2,1,3-benzothiadiazol-4-yl]methylene}malononitrile 
• 1393343-59-3 2-{[7-(5-(N,N-diphenyl)aminothiophen-2-yl)-2,1,3-benzothiadiazol-4-yl]methylene}malononitrile 
• 1393343-60-6 2-{[7-(4-(N,N-diphenyl)aminophenyl)-2,1,3-benzothiadiazol-4-yl]methylene}malononitrile 
• 1393343-58-2 2-[(7-(4-[N,N-bis(4-methylphenyl)amino]phenyl)-2,1,3-benzothia-diazol-4-yl)methylene]propane-dinitrile 
• 1419639-20-5 2-{[7-(2-fluoro-4-(N,N-di-p-tolyl)aminophenyl)-2,1,3-benzothiadiazol-4-yl]methylene}malononitrile 

Relevant articles and documents

Organic light-emitting material containing benzo[c][1,2,5]thiadiazole derivative receptor structural unit and application

The invention provides an organic light-emitting material based on a donor-receptor structure of a benzo[c][1,2,5]thiadiazole-4-aldehyde group receptor and a 2-(benzo[c][1,2,5]thiadiazole-4-methylene)malononitrile receptor and application thereof. The organic light-emitting material is a receptor-donor separation system, wherein the receptor is benzo[c][1,2,5]thiadiazole-4-aldehyde or 2-(benzo[c][1,2,5]thiadiazole-4-methylene) malononitrile, and a donor is carbazole and a derivative or benzoxazine and the like. The lowest unoccupied molecular orbital (LUMO) in the material is located in the receptor, and the highest occupied molecular orbital (HOMO) in the material is located in the donor, so that the molecular orbital energy level of the luminescent material can be effectively regulated and controlled through electrical regulation of the receptor structure and the donor. By regulating and controlling the structure of the light-emitting material or the electron donating capability of the donor, the light-emitting color of material molecules can be conveniently regulated. The organic light-emitting material has the characteristic that the light-emitting color is easy to adjust, andcan be used as a light-emitting material for preparing an OLED device.

Compounds for organic thin-film solar cells and organic thin-film solar cells

Provided are compounds with a donor moiety, a first acceptor moiety and a second acceptor moiety, as shown by Formula (I): With the unique molecular design, compounds of Formula (I) can provide a desirable power conversion efficiency. Moreover, this invention also provides organic thin-film solar cells comprising the above-mentioned compounds.

New low bandgap molecules based on ethylene-separated benzothiadiazoles: Synthesis and bandgap comparison

New ethylene-separated benzothiadiazoles were synthesized for the first time by using a facile procedure, and they showed lower bandgaps than the reported benzothiadiazole-containing compounds. This new benzothiadiazole- containing unit could be introduced into the backbone of the π-conjugated small molecules or polymers to develop new materials with a low bandgap that may have potential applications in optoelectronic fields.