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6-Quinolinol, 8-methyl-

Base Information Edit
  • Chemical Name:6-Quinolinol, 8-methyl-
  • CAS No.:64165-33-9
  • Molecular Formula:C10H9NO
  • Molecular Weight:159.18500
  • Hs Code.:
  • Mol file:64165-33-9.mol
6-Quinolinol, 8-methyl-

Synonyms:8-Methyl-quinolin-6-ol;8-Methyl-chinolin-6-ol;6-Quinolinol, 8-methyl-;

Suppliers and Price of 6-Quinolinol, 8-methyl-
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
  • Crysdot
  • 8-Methylquinolin-6-ol 97%
  • 1g
  • $ 842.00
  • Chemenu
  • 8-Methylquinolin-6-ol 97%
  • 1g
  • $ 795.00
Total 6 raw suppliers
Chemical Property of 6-Quinolinol, 8-methyl- Edit
Chemical Property:
  • PSA:33.12000 
  • LogP:2.24880 
Purity/Quality:

NLT 98% *data from raw suppliers

8-Methylquinolin-6-ol 97% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 6-Quinolinol, 8-methyl-

There total 5 articles about 6-Quinolinol, 8-methyl- 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 glucose dehydrogenase; D-glucose; cytochrome P450 enzyme CYP102A1 R47L/Y51F/H171L/I263G/Q307H/N319Y/A328L mutant; C21H25N7O17P3(3-)*2H(1+)*Na(1+); In aq. phosphate buffer; ethanol; at 20 ℃; for 16h; pH=8.4; Catalytic behavior; Enzymatic reaction;
DOI:10.1002/anie.201904157
Guidance literature:
With boron tribromide; In dichloromethane; at 0 - 20 ℃; for 6h;
DOI:10.1039/d1cc04418d
Guidance literature:
Multi-step reaction with 2 steps
1: sulfuric acid; sodium iodide / 6 h / 140 °C
2: boron tribromide / dichloromethane / 6 h / 0 - 20 °C
With sulfuric acid; boron tribromide; sodium iodide; In dichloromethane;
DOI:10.1039/d1cc04418d
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