9H-Carbazole, 1,6-dichloro-

Base Information

• Chemical Name: 9H-Carbazole, 1,6-dichloro-
• CAS No.: 64389-47-5
• Molecular Formula: C12H7Cl2N
• Molecular Weight: 236.1
• DSSTox Substance ID: DTXSID40471775
• Nikkaji Number: J848.321C
• Wikidata: Q82300430

Synonyms:64389-47-5;9H-Carbazole, 1,6-dichloro-;DTXSID40471775

Chemical Property of 9H-Carbazole, 1,6-dichloro-

Chemical Property:

• XLogP3: 4.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 234.9955546
• Heavy Atom Count: 15
• Complexity: 246

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1=CC2=C(C(=C1)Cl)NC3=C2C=C(C=C3)Cl

Technology Process of 9H-Carbazole, 1,6-dichloro-

There total 2 articles about 9H-Carbazole, 1,6-dichloro- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

N-chlorocarbazole (105598-33-2) → 1,6-dichlorocarbazole (64389-47-5) + 1-chlorocarbazole (5599-70-2) + 3,6-dichloro-9H-carbazole (5599-71-3) + 9H-carbazole (86-74-8,105184-46-1,97960-57-1)

Guidance literature:

In methanol; at 39 ℃;

DOI:10.1002/jhet.5570340327

Reference yield:

N-chlorocarbazole (105598-33-2) → 1,6-dichlorocarbazole (64389-47-5) + 1-chlorocarbazole (5599-70-2) + 3-chloro-9H-carbazole (2732-25-4) + 3,6-dichloro-9H-carbazole (5599-71-3) + 9H-carbazole (86-74-8,105184-46-1,97960-57-1)

Guidance literature:

In methanol; dichloromethane; for 1h; Product distribution; Mechanism; Heating; var. times, also in the presence of acid or basic reaction partner;

DOI:10.1021/jo00378a002

upstream raw materials:

N-chlorocarbazole

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