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Name: 4,7-dibromo-2,1,3-benzothiadiazole-5,6-diamine  

CAS NO: 141215-32-9

MF: C6H4Br2N4S

MW: 324

BP:423.0±40.0 °C(Predicted)

Density:2.375±0.06 g/cm3(Predicted)

Appearance:Tawny powder

Purity: 97% min

Package: 25g, 100g, 500g, bulk package

Application:365bet娱乐 intermediate

4,7-Dibromobenzo[c][1,2,5]thiadiazole-5,6-diamine (DBTD) CAS：141215-32-9 is an important and highly versatile organic molecule with a wide range of applications in the fields of chemistry, biochemistry and pharmacology. It is a derivative of benzo[c][1,2,5]thiadiazole, and it is used as a building block in the synthesis of various organic molecules. DBTD has been used in the synthesis of various drugs, as well as in the development of new drugs and drug delivery systems. It has also been used in the synthesis of various polymers, dyes, and other materials. DBTD is a highly reactive molecule, and its reactivity has been exploited in various chemical reactions. 

Synthesis and Material Development

4,7-Dibromobenzo[c][1,2,5]thiadiazole-5,6-diamine is utilized in the synthesis of various materials. For instance, it's used in the one-pot synthesis of low bandgap materials via palladium-catalyzed coupling reactions.

Photovoltaic and Light-Emitting Applications

Its derivatives play a significant role in the development of photovoltaic materials. For example, dibromoderivatives of benzofused chalcogen-nitrogen heterocycles, including 4,7-Dibromobenzo[c][1,2,5]thiadiazole, are important precursors in synthesizing photovoltaic materials.

Advancements in Organic Synthesis

The compound aids in the development of novel synthetic pathways. An improved synthesis approach using 4,7-dibromobenzo[d][1,2,3]thiadiazole has been developed, leading to high electron conductivity due to the stability of the molecule in the excited state. This process is crucial for designing promising photovoltaic materials .

Contributions to Polymer Science

The compound is instrumental in synthesizing hyperbranched conjugated polymers. It's used in Suzuki coupling polymerization to create polymers with enhanced optical properties, crucial for various applications in polymer science.

Catalysis and Reaction Mechanisms

4,7-Dibromobenzo[c][1,2,5]thiadiazole-5,6-diamine plays a role in understanding catalytic mechanisms.

Other name:

4,7-dibromobenzo[c][1,2,5]thiadiazole-5,6-diamine;

2,1,3-Benzothiadiazole-5,6-diamine,4,7-dibromo;

5,6-diamino-4,7-dibromobenzo[c][1,2,5]-thiadiazole;

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