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Home  > 6,6'-Dibromo-1,1'-bis(2-ethylhexyl)-[3,3'-biindolinylidene]-2,2'-dione

AA19359

1147124-23-9 | 6,6'-Dibromo-1,1'-bis(2-ethylhexyl)-[3,3'-biindolinylidene]-2,2'-dione

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $66.00 $46.00 -   +
1g 97% in stock $163.00 $114.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA19359
Chemical Name: 6,6'-Dibromo-1,1'-bis(2-ethylhexyl)-[3,3'-biindolinylidene]-2,2'-dione
CAS Number: 1147124-23-9
Molecular Formula: C32H40Br2N2O2
Molecular Weight: 644.4802
MDL Number: MFCD28125575
SMILES: CCCCC(CN1C(=O)C(=C2c3ccc(cc3N(C2=O)CC(CCCC)CC)Br)c2c1cc(Br)cc2)CC

 

Upstream Synthesis Route
  • 6,6'-Dibromo-1,1'-bis(2-ethylhexyl)-[3,3'-biindolinylidene]-2,2'-dione is a versatile compound commonly used in chemical synthesis due to its unique properties. This compound is especially valuable in the field of organic synthesis as a key component in the development of new materials, functional molecules, and pharmaceutical compounds. Its high reactivity and stability make it ideal for the construction of complex molecular structures through various synthetic routes. In particular, 6,6'-Dibromo-1,1'-bis(2-ethylhexyl)-[3,3'-biindolinylidene]-2,2'-dione is utilized in the formation of novel polymers, organic semiconductors, and fluorescent dyes. Its ability to undergo diverse chemical reactions, such as cross-coupling reactions and cycloaddition reactions, further enhances its utility in organic synthesis processes. Additionally, its presence in the synthesis of biologically active compounds highlights its significance in medicinal chemistry research. By serving as a crucial building block in the creation of advanced organic compounds, 6,6'-Dibromo-1,1'-bis(2-ethylhexyl)-[3,3'-biindolinylidene]-2,2'-dione plays a pivotal role in expanding the horizons of chemical synthesis applications.
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