7-Aminofluoranthene

Base Information

• Chemical Name: 7-Aminofluoranthene
• CAS No.: 13177-27-0
• Molecular Formula: C16H11N
• Molecular Weight: 217.2652
• UNII: 29RFA5UH29
• DSSTox Substance ID: DTXSID50157199
• Mol file: 13177-27-0.mol

Synonyms:7-Aminofluoranthene;7-FLUORANTHENAMINE;13177-27-0;CCRIS 7012;BRN 2105581;29RFA5UH29;UNII-29RFA5UH29;DTXSID50157199;LS-69110

Chemical Property of 7-Aminofluoranthene

Chemical Property:

• Vapor Pressure: 3.58E-08mmHg at 25°C
• Boiling Point: 446.7°C at 760 mmHg
• Flash Point: 250.6°C
• Density: 1.322g/cm³
• XLogP3: 4.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 217.089149355
• Heavy Atom Count: 17
• Complexity: 300

Purity/Quality:

97% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC2=C3C(=C1)C4=C(C3=CC=C2)C(=CC=C4)N

Technology Process of 7-Aminofluoranthene

There total 16 articles about 7-Aminofluoranthene 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: 95.0%

7-nitrofluoranthene (13177-31-6) → 7-Amino-fluoranthen (13177-27-0)

Guidance literature:

With hydrazine hydrate; nickel; In ethanol; for 2h; Heating;

DOI:10.1002/recl.19921110701

Reference yield:

9H-fluorene (86-73-7) → 7-Amino-fluoranthen (13177-27-0)

Guidance literature:

Multi-step reaction with 9 steps

2: 95 percent / 20percent aq. KOH / ethanol / 48 h / Heating

3: thionyl chloride (SOCl₂) / 1 h / Heating

4: AlCl₃ / CH₂Cl₂ / 0.33 h / 0 °C

5: 16 percent / ammonium nitrate, trifluoroacetic anhydride / acetonitrile / Ambient temperature

6: NaBH₄ / CH₂Cl₂; methanol / 2 h / Ambient temperature

7: p-toluenesulfonic acid / toluene / 3 h / Heating

8: 56 percent / dichlorodicyanobenzoquinone (DDQ) / toluene / 2 h / Heating

9: 95 percent / hydrazine monohydrate / Raney Ni / ethanol / 2 h / Heating

With potassium hydroxide; sodium tetrahydroborate; aluminium trichloride; thionyl chloride; ammonium nitrate; toluene-4-sulfonic acid; hydrazine hydrate; trifluoroacetic anhydride; 2,3-dicyano-5,6-dichloro-p-benzoquinone; nickel; In methanol; ethanol; dichloromethane; toluene; acetonitrile;

DOI:10.1002/recl.19921110701

Reference yield:

3-(fluoren-9-yl)propionic acid (97634-43-0) → 7-Amino-fluoranthen (13177-27-0)

Guidance literature:

Multi-step reaction with 7 steps

1: thionyl chloride (SOCl₂) / 1 h / Heating

2: AlCl₃ / CH₂Cl₂ / 0.33 h / 0 °C

3: 16 percent / ammonium nitrate, trifluoroacetic anhydride / acetonitrile / Ambient temperature

4: NaBH₄ / CH₂Cl₂; methanol / 2 h / Ambient temperature

5: p-toluenesulfonic acid / toluene / 3 h / Heating

6: 56 percent / dichlorodicyanobenzoquinone (DDQ) / toluene / 2 h / Heating

7: 95 percent / hydrazine monohydrate / Raney Ni / ethanol / 2 h / Heating

With sodium tetrahydroborate; aluminium trichloride; thionyl chloride; ammonium nitrate; toluene-4-sulfonic acid; hydrazine hydrate; trifluoroacetic anhydride; 2,3-dicyano-5,6-dichloro-p-benzoquinone; nickel; In methanol; ethanol; dichloromethane; toluene; acetonitrile;

DOI:10.1002/recl.19921110701

upstream raw materials:

Fluoranthren-7-carbonsaeure

7-nitrofluoranthene

2-(naphthalen-1-yl)phenylamine

9H-fluorene