110590-84-6 | 2,9-Di(tridecan-7-yl)anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetraone

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$30.00	$21.00
250mg	97%	in stock	$67.00	$47.00

Description

• Catalog Number: AE13218
• Chemical Name: 2,9-Di(tridecan-7-yl)anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetraone
• CAS Number: 110590-84-6
• Molecular Formula: C50H62N2O4
• Molecular Weight: 755.0382800000009
• MDL Number: MFCD08702668
• SMILES: CCCCCCC(N1C(=O)c2ccc3c4c2c(C1=O)ccc4c1c2c3ccc3c2c(cc1)C(=O)N(C3=O)C(CCCCCC)CCCCCC)CCCCCC

Upstream Synthesis Route

The compound $name$ is a unique anthraisoquinolinetetraone derivative that finds significant application in chemical synthesis. Its structure, characterized by the presence of tridecan-7-yl side chains and multiple fused rings, imparts distinctive properties that make it valuable in various synthetic pathways.In chemical synthesis, $name$ serves as a versatile building block for the construction of complex organic molecules. The presence of the anthraquinone and isoquinoline moieties, along with the tetraone functionality, facilitates diverse reactivity and allows for the formation of intricate molecular structures. The tridecan-7-yl substituents offer steric effects that can influence regioselectivity and stereochemistry in reactions involving $name$.Furthermore, the unique structural features of $name$ enable it to participate in a range of transformation reactions, including oxidation, reduction, and condensation processes. Its ability to act as both a ligand and a reactive center in chemical transformations broadens its utility in the synthetic toolbox.Overall, the incorporation of 2,9-Di(tridecan-7-yl)anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetraone in chemical synthesis offers exciting possibilities for the creation of novel compounds and the exploration of new synthetic methodologies.