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8-Bromophenanthridin-6-ol

Base Information Edit
  • Chemical Name:8-Bromophenanthridin-6-ol
  • CAS No.:26689-66-7
  • Molecular Formula:C13H8 Br N O
  • Molecular Weight:274.1127
  • Hs Code.:
  • NSC Number:109627
  • DSSTox Substance ID:DTXSID10296497
  • Nikkaji Number:J3.544.117D
  • Wikidata:Q82037125
  • Mol file:26689-66-7.mol
8-Bromophenanthridin-6-ol

Synonyms:8-bromophenanthridin-6-ol;26689-66-7;NSC109627;SCHEMBL3503005;SCHEMBL20227579;DTXSID10296497;PRZKTRKRIPLYEK-UHFFFAOYSA-N;NSC-109627

Suppliers and Price of 8-Bromophenanthridin-6-ol
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 2 raw suppliers
Chemical Property of 8-Bromophenanthridin-6-ol Edit
Chemical Property:
  • Vapor Pressure:0.000115mmHg at 25°C 
  • Boiling Point:336°C at 760 mmHg 
  • Flash Point:157°C 
  • Density:1.568g/cm3 
  • XLogP3:3.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:0
  • Exact Mass:272.97893
  • Heavy Atom Count:16
  • Complexity:294
Purity/Quality:

99%min *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C3=C(C=C(C=C3)Br)C(=O)N2
Technology Process of 8-Bromophenanthridin-6-ol

There total 3 articles about 8-Bromophenanthridin-6-ol 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:
Guidance literature:
With 1-(2-hydroxyethyl)piperazine; potassium tert-butylate; In 1,3,5-trimethyl-benzene; at 150 ℃; for 24h; Sealed tube; Inert atmosphere;
DOI:10.1021/acs.joc.0c01019
Guidance literature:
Multi-step reaction with 3 steps
1: thionyl chloride / tetrahydrofuran / Reflux; Inert atmosphere
2: triethylamine; dmap / dichloromethane / 6 h / 0 - 20 °C / Inert atmosphere
3: 1-(2-hydroxyethyl)piperazine; potassium tert-butylate / 1,3,5-trimethyl-benzene / 24 h / 150 °C / Sealed tube; Inert atmosphere
With 1-(2-hydroxyethyl)piperazine; dmap; thionyl chloride; potassium tert-butylate; triethylamine; In tetrahydrofuran; dichloromethane; 1,3,5-trimethyl-benzene;
DOI:10.1021/acs.joc.0c01019
Guidance literature:
Multi-step reaction with 2 steps
1: triethylamine; dmap / dichloromethane / 6 h / 0 - 20 °C / Inert atmosphere
2: 1-(2-hydroxyethyl)piperazine; potassium tert-butylate / 1,3,5-trimethyl-benzene / 24 h / 150 °C / Sealed tube; Inert atmosphere
With 1-(2-hydroxyethyl)piperazine; dmap; potassium tert-butylate; triethylamine; In dichloromethane; 1,3,5-trimethyl-benzene;
DOI:10.1021/acs.joc.0c01019
Refernces Edit
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