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6-Hydroxybenzbromarone

Base Information Edit
  • Chemical Name:6-Hydroxybenzbromarone
  • CAS No.:152831-00-0
  • Molecular Formula:C17H12Br2O4
  • Molecular Weight:440.088
  • Hs Code.:
  • UNII:4M7NUR5V9E
  • Nikkaji Number:J570.202J
  • Pharos Ligand ID:G4ZGJ3CDTCXP
  • ChEMBL ID:CHEMBL1767079
  • Mol file:152831-00-0.mol
6-Hydroxybenzbromarone

Synonyms:6-hydroxybenzbromarone

Suppliers and Price of 6-Hydroxybenzbromarone
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 7 raw suppliers
Chemical Property of 6-Hydroxybenzbromarone Edit
Chemical Property:
  • XLogP3:5.2
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:3
  • Exact Mass:439.90818
  • Heavy Atom Count:23
  • Complexity:434
Purity/Quality:

99%, *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCC1=C(C2=C(O1)C=C(C=C2)O)C(=O)C3=CC(=C(C(=C3)Br)O)Br
Technology Process of 6-Hydroxybenzbromarone

There total 7 articles about 6-Hydroxybenzbromarone 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 aluminum (III) chloride; ethanethiol; In dichloromethane; for 1.5h; Cooling with ice/NaCl bath;
DOI:10.1021/jm1015022
Guidance literature:
Multi-step reaction with 4 steps
1: tin(IV) chloride / carbon disulfide / 5 - 20 °C / Inert atmosphere; Cooling with ice
2: sodium thioethylate / N,N-dimethyl-formamide / 1 h / 105 - 110 °C
3: N-Bromosuccinimide / dichloromethane; N,N-dimethyl-formamide / 20 h / 20 °C / Cooling with ice-brine bath
4: aluminum (III) chloride; ethanethiol / dichloromethane / 1.5 h / Cooling with ice/NaCl bath
With aluminum (III) chloride; N-Bromosuccinimide; tin(IV) chloride; ethanethiol; sodium thioethylate; In carbon disulfide; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm1015022
Guidance literature:
Multi-step reaction with 3 steps
1: sodium thioethylate / N,N-dimethyl-formamide / 1 h / 105 - 110 °C
2: N-Bromosuccinimide / dichloromethane; N,N-dimethyl-formamide / 20 h / 20 °C / Cooling with ice-brine bath
3: aluminum (III) chloride; ethanethiol / dichloromethane / 1.5 h / Cooling with ice/NaCl bath
With aluminum (III) chloride; N-Bromosuccinimide; ethanethiol; sodium thioethylate; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm1015022
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