Indolo[3,2-b]carbazole

Catalog Number

ACM6336329-2

CAS

6336-32-9

Structure

Synonyms

5,11-Dihydroindolo[3,2-B]Carbazole

IUPAC Name

5,11-dihydroindolo[3,2-b]carbazole

Molecular Weight

254.29

Molecular Formula

C18H10N2

Canonical SMILES

C1=CC=C2C(=C1)C3=CC4=C(C=C3N2)C5=CC=CC=C5N4

InChI

InChI=1S/C18H12N2/c1-3-7-15-11(5-1)13-9-18-14(10-17(13)19-15)12-6-2-4-8-16(12)20-18/h1-10,19-20H

InChI Key

YCPBCVTUBBBNJJ-UHFFFAOYSA-N

Boiling Point

460 °C

Melting Point

569.8 ± 23.0 °C

Purity

95%+

Density

1.404 ± 0.06 g/ml

Application

Indolo[3,2-b]carbazole serves as a crucial component in enhancing the performance of various electronic devices, including organic light-emitting diodes (OLEDs), organic field-effect transistors (OFETs), and solar cells. Its large planar and rigid conjugated structure, characterized by fused alternating three benzene and two pyrrole rings, makes it a heterocyclic analogue of pentacene, and an effective nitrogen-containing electron-rich heteroacene. Its synthesis is pivotal in creating oligomers and polymers that exhibit remarkable electrical, optical, and magnetic properties. Due to its electron-donating capabilities, Indolo[3,2-b]carbazole is frequently used as a hole transporting, charge injection, host, and electroluminescent material, offering exceptional thermal, chemical, and environmental stability, making it highly suitable for application in advanced electronic materials.

• Catalog Number: ACM6336329-2
• CAS: 6336-32-9
• Synonyms: 5,11-Dihydroindolo[3,2-B]Carbazole
• IUPAC Name: 5,11-dihydroindolo[3,2-b]carbazole
• Molecular Weight: 254.29
• Molecular Formula: C18H10N2
• Canonical SMILES: C1=CC=C2C(=C1)C3=CC4=C(C=C3N2)C5=CC=CC=C5N4
• InChI: InChI=1S/C18H12N2/c1-3-7-15-11(5-1)13-9-18-14(10-17(13)19-15)12-6-2-4-8-16(12)20-18/h1-10,19-20H
• InChI Key: YCPBCVTUBBBNJJ-UHFFFAOYSA-N
• Boiling Point: 460 °C
• Melting Point: 569.8 ± 23.0 °C
• Purity: 95%+
• Density: 1.404 ± 0.06 g/ml
• Application: Indolo[3,2-b]carbazole serves as a crucial component in enhancing the performance of various electronic devices, including organic light-emitting diodes (OLEDs), organic field-effect transistors (OFETs), and solar cells. Its large planar and rigid conjugated structure, characterized by fused alternating three benzene and two pyrrole rings, makes it a heterocyclic analogue of pentacene, and an effective nitrogen-containing electron-rich heteroacene. Its synthesis is pivotal in creating oligomers and polymers that exhibit remarkable electrical, optical, and magnetic properties. Due to its electron-donating capabilities, Indolo[3,2-b]carbazole is frequently used as a hole transporting, charge injection, host, and electroluminescent material, offering exceptional thermal, chemical, and environmental stability, making it highly suitable for application in advanced electronic materials.