5,12-Dibromo-2,9-dioctylanthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetraone

• CAT Number: L029029
• CAS Number: 209111-67-1
• Molecular Formula: C40H40Br2N2O4
• Molecular Weight: 772.60
• Purity: ≥95%
• IUPAC Name: 11,22-dibromo-7,18-dioctyl-7,18-diazaheptacyclo[14.6.2.22,5.03,12.04,9.013,23.020,24]hexacosa-1(22),2,4,9,11,13(23),14,16(24),20,25-decaene-6,8,17,19-tetrone
• InChI: InChI=1S/C40H40Br2N2O4/c1-3-5-7-9-11-13-19-43-37(45)25-17-15-23-34-30(42)22-28-32-26(38(46)44(40(28)48)20-14-12-10-8-6-4-2)18-16-24(36(32)34)33-29(41)21-27(39(43)47)31(25)35(23)33/h15-18,21-22H,3-14,19-20H2,1-2H3
• InChIKey: JFVLXCZVJSJPFG-UHFFFAOYSA-N
• SMILES: CCCCCCCCN1C(=O)C2=C3C(=CC(=C4C3=C(C=C2)C5=C(C=C6C7=C(C=CC4=C57)C(=O)N(C6=O)CCCCCCCC)Br)Br)C1=O

5,12-Dibromo-2,9-dioctylanthra[2,1,9-def:6,5,10-d’e’f’]diisoquinoline-1,3,8,10(2H,9H)-tetraone（Cat No.:L029029）is a highly complex organic molecule, characterized by an anthraquinone structure fused with two isoquinoline units and substituted with bromo and octyl groups. This structure offers multifaceted chemical properties, useful in advanced material science for creating organic semiconductors and photovoltaic cells. The bromine atoms facilitate further chemical modifications through coupling reactions, while the octyl groups enhance solubility in organic solvents. This compound is pivotal in the development of high-performance organic electronics, contributing to advancements in OLED technology and organic solar cells.