185011-61-4

Basic information

• Product Name: 9-Ethyl-N⁴-(9-ethyl-9H-carbazol-3-yl)-9H-carbazole-3,4-diamine
• Synonyms: 9-Ethyl-N⁴-(9-ethyl-9H-carbazol-3-yl)-9H-carbazole-3,4-diamine
• CAS NO: 185011-61-4
• Molecular Weight: 418.541
• Mol File: 185011-61-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 9-Ethyl-N⁴-(9-ethyl-9H-carbazol-3-yl)-9H-carbazole-3,4-diamine(CAS DataBase Reference)
• NIST Chemistry Reference: 9-Ethyl-N⁴-(9-ethyl-9H-carbazol-3-yl)-9H-carbazole-3,4-diamine(185011-61-4)
• EPA Substance Registry System: 9-Ethyl-N⁴-(9-ethyl-9H-carbazol-3-yl)-9H-carbazole-3,4-diamine(185011-61-4)

Safety Data

• Hazardous Substances Data: 185011-61-4(Hazardous Substances Data)

Upstream product

• 82298-50-8 9,9'-diethyl-Z-3,3'-azocarbazole 
• 104563-32-8 3-azoxy-9-ethylcarbazole 
• 86-20-4 9-ethyl-3-nitro-carbazole 
• 64-17-5 ethanol 

Downstream Products

• 95600-18-3 C₂₈H₂₂N₄ 

Relevant articles and documents

Alkali-induced Formation of ortho-Semidines from 3-Nitro- and 3-Azocarbazoles - Synthesis of 8,16-Dialkyldiindolo[3,2-a,d]phenazines

The ortho-semidines 9-alkyl-4-(9-alkylcarbazol-3-ylamino)-3-aminocarbazoles (2a-d) are formed either by reduction of 9-alkyl-3-nitro-carbazoles (1a-d) or of the azo-(6) or the azoxycarbazoles (7) with zinc in alkaline alcoholic solution. It could be shown by cross experiments that the semidines 2 result from an intramolecular rearrangement. The compounds 2a-d are oxidized by air or H2O2 to the 8,16-dialkyldiindolo[3,2-a,d]phenazines (3a-d). Reduction of 1a-c with Raney-alloy affords the 9-alkyl-3-azoxycarbazoles 7a-c in good yields.