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Home  > 4,9-Dibromo-2,7-bis(2-ethylhexyl)benzo[lmn][3,8]phenanthroline-1,3,6,8(2h,7h)-tetraone

AE21604

1088205-02-0 | 4,9-Dibromo-2,7-bis(2-ethylhexyl)benzo[lmn][3,8]phenanthroline-1,3,6,8(2h,7h)-tetraone

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $34.00 $24.00 -   +
5g 98% in stock $365.00 $256.00 -   +

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*All prices are in USD.

Description
Catalog Number: AE21604
Chemical Name: 4,9-Dibromo-2,7-bis(2-ethylhexyl)benzo[lmn][3,8]phenanthroline-1,3,6,8(2h,7h)-tetraone
CAS Number: 1088205-02-0
Molecular Formula: C30H36Br2N2O4
Molecular Weight: 648.4258
MDL Number: MFCD27923032
SMILES: CCCCC(Cn1c(=O)c2cc(Br)c3c4c2c(c1=O)c(Br)cc4c(=O)n(c3=O)CC(CCCC)CC)CC

 

Upstream Synthesis Route
  • 4,9-Dibromo-2,7-bis(2-ethylhexyl)benzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetraone, commonly referred to as $name$, is a versatile compound widely used in chemical synthesis. This compound is known for its ability to act as a powerful catalyst in a variety of organic transformations. One key application of $name$ in chemical synthesis is in the formation of complex organic molecules through C-C bond formation reactions. Due to its unique structure and reactivity, $name$ can facilitate the construction of carbon-carbon bonds in a selective and efficient manner. This makes it a valuable tool for chemists working on the synthesis of natural products, pharmaceuticals, and other fine chemicals.Moreover, $name$ can also serve as a ligand in transition metal catalyzed reactions, enabling the activation of otherwise inert chemical bonds. This property allows for the development of new synthetic methodologies and the rapid assembly of structurally diverse compounds.In summary, the use of 4,9-Dibromo-2,7-bis(2-ethylhexyl)benzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetraone in chemical synthesis offers chemists a powerful tool to streamline complex reactions, accelerate synthetic pathways, and access novel chemical scaffolds.
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